81. Dr. Koop - Beckwith-Wiedemann Syndrome beckwithwiedemann syndrome in the newborn is a consistent group of findings ofunknown cause and is characterized by large tongue (macroglossia), http://www.drkoop.com/ency/93/ImagePages/17076.html

Home Health Reference Beckwith-Wiedemann syndrome Jul 29, 2005 Search: Dr.Koop MEDLINE Diseases Symptoms Procedures Natural Medicine ... Drug Library Inside DrKoop News Archive Animations Health Videos Health Tools ... Newsletters Beckwith-Wiedemann syndrome Beckwith-Wiedemann syndrome in the newborn is a consistent group of findings of unknown cause and is characterized by large tongue (macroglossia), large organs (visceromegaly), large body size (macrosomia), hernia of the navel (omphalocele) and small head (microcephaly). New Features Fewer Migraines Skin Cancer Atkins/Low Carb Diets Learn More About Migraines * All Health Centers * Acne Addictions AIDS/HIV Alcohol Abuse Allergies Alternative Medicine Alzheimer's Arthritis Asthma Attention Deficit Disorder (ADHD) Backache Bipolar Affective Disorder Birth Control Blood Blood Pressure Bone/Joint/Tendon Bowel Brain Breast cancer Cancer Cerebral Palsy Cholesterol Cramps Crohn's Disease Cysts Dental/Oral Depression Diabetes Diet, Fitness, Looks Disabled/Special Needs Drug Abuse Ear/Nose/Throat Eating/Appetite Eczema Encephalitis Eye/Vision Fatigue Fever Flu Food Poisoning Foot Gallbladder Gastrointestinal Genetic/Congenital GERD/Heartburn Hair Loss Hair/Scalp Headache Hearing Heart Disease, Stroke

82. Faculty Of 1000 Biology | Beckwith-Wiedemann Syndrome And IVF: A Case-control St beckwithwiedemann syndrome and IVF a case-control study. Halliday J, Oke K,Breheny S, Algar E, J Amor D Am J Hum Genet 2004 Sep 75(3)526-8 http://www.facultyof1000.com/article/15284956/evaluation

Subscription Info Institutional Access Free Trial F1000 walkthrough ... About F1000 Beckwith-Wiedemann syndrome and IVF: a case-control study. Halliday J, Oke K, Breheny S, Algar E, J Amor D Am J Hum Genet 2004 Sep "This paper reports the first case-control study of the incidence..." Evaluated by Faculty of 1000 Biology member Carmen Sapienza (Temple University School of Medicine, United States) To see the full evaluation, choose from the options below: Faculty of 1000 Biology Essential, rapid post-publication evaluation of the most important papers in biology by over 1900 of the world's top scientists [see a sample evaluation You can: Customize the site and receive tailored e-mail alerts [ more "This is really going to help busy scientists find the gems amongst the mounds of rubble!" Keith Roberts (John Innes Centre, UK) Personal access Existing subscribers Log in here E-mail Password Free 7 day trial Subscribe Institutional access Recommend to your librarian 80% of the world's top institutions subscribe! Log in via Athens If you are registered and have trouble logging in, email us:

83. Disease - Beckwith-Wiedemann Syndrome - Detroit, Michigan Disease beckwith-wiedemann syndrome - courtesy of Henry Ford Health System ofDetroit, Michigan. http://www.henryfordhealth.org/12207.cfm

3D Tour of the Vattikuti Institute About the Institute The Vattikuti Institute Prostatectomy Prostate Cancer ... Health Encyclopedia Health Encyclopedia Back to main Health Information page Disease - Beckwith-Wiedemann syndrome Beckwith-Wiedemann syndrome Metopic ridge Definition: Beckwith-Wiedemann syndrome is a consistent grouping of findings of unknown etiology (cause) and characterized by a large tongue ( macroglossia ), large organs ( visceromegaly ) and large body size ( macrosomia umbilical hernia or omphalocele (hernia of the navel), and low blood sugar in the newborn (neonatal hypoglycemia Causes And Risk: The cause of Beckwith-Wiedemann syndrome is unknown, but it appears to be genetic. Some cases may be associated with a defect in chromosome number 11. Affected children are often large at birth. Many have an abdominal wall defect, such as an umbilical hernia or omphalocele. They have a characteristic facial appearance with a gaping mouth and large tongue. Infancy can be a critical period because of low blood sugar (hypoglycemia)

84. Beckwith-Wiedemann Syndrome (BWS) - Patient UK beckwithwiedemann syndrome (BWS) - Patient UK. A directory of UK health, disease,illness and related medical websites that provide patient information. http://www.patient.co.uk/showdoc/40001350/

PatientPlus articles are written for doctors and so the language can be technical. However, some people find that they add depth to the articles found in the other sections of this website which are written for non-medical people. Beckwith-Wiedemann Syndrome (BWS) An overgrowth disorder with macroglossia, abdominal wall defects and visceromegaly. First described in 1963 by Dr J Bruce Beckwith, a paediatric pathologist working in California. Also in 1964 by Dr HR Wiedemann, a geneticist from Kiel in Germany. The severity of affect on the child is highly variable, with the majority minimally affected. Aetiology The underlying cause is unclear. 80% of cases have genotypic abnormalities on the distal portion of chromosome 11p. The reported pattern of inheritance is autosomal dominance with variable expression. There is contiguous gene duplication at band 11p.15.5. This is always derived from the patients father, whereas translocation and inversion is invariably derived from the mother. There appears to be aberrant genomic imprinting resulting from a defective or absent copy of the maternally derived gene. Most sporadic cases lack apparent cytogenetic abnormalities. Only 2% carry inversions, translocations or deletions. 20% of sporadic cases have uniparental disomy

85. Long-Term Changes In Dentoskeletal Pattern In A Case With Beckwith-Wiedemann Syn Macroglossia is the predominent finding in beckwithwiedemann syndrome (97%) A genetic diagnosis is now possible for beckwith-wiedemann syndrome.12,13 A http://www.angle.org/anglonline/?request=get-document&issn=0003-3219&volume=070&

86. Beckwith-Wiedemann Syndrome beckwithwiedemann syndrome is a consistent grouping of findings of unknownetiology (cause) and characterized by a large tongue (macroglossia), http://www.pennhealth.com/ency/article/001186.htm

Appointments Medical Services Health Information Find a Doctor Search: Search Encyclopedia: List of Topics Print This Page  Endocrinology Beckwith-Wiedemann syndrome Beckwith-Wiedemann syndrome Metopic ridge Definition: Beckwith-Wiedemann syndrome is characterized by a consistent set of symptoms including a large tongue ( macroglossia ), large organs ( visceromegaly ), large body size ( macrosomia umbilical hernia or omphalocele (hernia of the navel), and low blood sugar in the newborn (neonatal hypoglycemia ). The cause is unknown. Causes, incidence, and risk factors: The cause of Beckwith-Wiedemann syndrome is unknown, but it appears to be genetic. Some cases may be associated with a defect in chromosome number 11. Affected children are often large at birth. Many have an abdominal wall defect, such as an umbilical hernia or omphalocele. They have a characteristic facial appearance with a gaping mouth and large tongue. Infancy can be a critical period because of low blood sugar (hypoglycemia), omphalocele (when present), and an increased rate of tumor development ( Wilm's tumor and adrenal carcinoma being most common).

87. Beckwith-Wiedemann Syndrome beckwithwiedemann syndrome - SWMC serving Vancouver Washington beckwith-wiedemann syndrome - Online Medical Encyclopedia courtesy of SouthwestWashington Medical Center, a Top 100 Hosptital award winner locacted in http://adam.about.com/encyclopedia/001186.htm

zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') zfs=0;zCMt='a61' About Healthcare Center IBS/Crohn's Disease Related Topics Beckwith-Wiedemann syndrome Healthcare Center Essentials A.D.A.M. Illustrated Health Encyclopedia In Depth Reports ... Help zau(256,140,140,'el','http://z.about.com/0/ip/417/C.htm','');w(xb+xb+' ');zau(256,140,140,'von','http://z.about.com/0/ip/496/6.htm','');w(xb+xb); Search Healthcare Center ENCYCLOPEDIA INDEX Injury Disease Nutrition Poison ... Z Beckwith-Wiedemann syndrome Overview Symptoms Treatment Prevention Definition: Beckwith-Wiedemann syndrome is a consistent grouping of findings of unknown etiology (cause) and characterized by a large tongue ( macroglossia ), large organs ( visceromegaly ) and large body size ( macrosomia umbilical hernia or omphalocele (hernia of the navel), and low blood sugar in the newborn (neonatal hypoglycemia Causes, incidence, and risk factors: The cause of Beckwith-Wiedemann syndrome is unknown, but it appears to be genetic. Some cases may be associated with a defect in chromosome number 11.

88. Beckwith-Wiedemann Syndrome: Ascertainment Of The Genetic Causes, Uniparental Di beckwithwiedemann syndrome ascertainment of the genetic causes, uniparentaldisomy, duplications, abnormal methylation patterns at LIT1, H19 or IGF2. http://www.research-projects.unizh.ch/med/unit42200/area313/p2311.htm

research project Beckwith-Wiedemann syndrome: ascertainment of the genetic causes, uniparental disomy, duplications, abnormal methylation patterns at LIT1, H19 or IGF2. Molecular genetic and clinical investigations of more than 100 patients. Contacts PD Dr. A. Baumer (Project Leader) baumer@medgen.unizh.ch Prof. A. Schinzel schinzel@medgen.unizh.ch Funding Source SNF Duration Jan 2002 to Jan 2011 Last Update Responsible Project Leader: PD Dr. A. Baumer Professor or Research Area Leader: Prof. Dr. Albert Schinzel Institute or Clinic: Faculty: Use the Google search engine to find descriptions of research projects For authorized person(s) only Comments to uni research page generation 03.04.2005

89. Beckwith-Wiedemann Syndrome beckwithwiedemann syndrome Medical.WebEnds.com. beckwith-wiedemann syndrome.Exomphalos-Macroglossia-Gigantism Syndrome; Wiedemann-Beckwith Syndrome; http://medical.webends.com/kw/Beckwith-Wiedemann Syndrome

Medical.WebEnds.com - Medical Terminology Dictionary A B C D ... Z WWW Medical.WebEnds.com Beckwith-Wiedemann Syndrome Exomphalos-Macroglossia-Gigantism Syndrome; Wiedemann-Beckwith Syndrome; Beckwith Wiedemann Syndrome; Exomphalos Macroglossia Gigantism Syndrome; Syndrome, Beckwith-Wiedemann; Syndrome, Exomphalos-Macroglossia-Gigantism A syndrome of multiple defects characterized primarily by umbilical hernia (HERNA, UMBILICAL), MACROGLOSSIA , and GIGANTISM and secondarily by visceromegaly, HYPOGLYCEMIA , and ear abnormalities Google links Processing time was 0.015657186508179 seconds.

90. Evolution Of The Beckwith-Wiedemann Syndrome Region In Vertebrates -- Paulsen Et Evolution of the beckwithwiedemann syndrome region in vertebrates. Martina Paulsen1 ,Tarang Khare , Christopher Burgard , Sascha Tierling and Jörn Walter http://www.genome.org/cgi/content/abstract/15/1/146

QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: Published online before print December 8, 2004, 10.1101/gr.2689805 Genome Research 15:146-153, 2005 ISSN 1088-9051/ $5.00 This Article Full Text Full Text (PDF) Supplemental Research Data ... The Chicken Genome All Versions of this Article: gr.2689805v1 most recent Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by Paulsen, M. Articles by Walter, J. Chicken Special/Letter Evolution of the Beckwith-Wiedemann syndrome region in vertebrates Martina Paulsen Tarang Khare Christopher Burgard Sascha Tierling and In the animal kingdom, genomic imprinting appears to be restricted

91. Resource Library Find Information On Beckwith-Wiedemann Syndrome Find information on beckwithwiedemann syndrome at MerckSource. Learn more aboutbeckwith-wiedemann syndrome, beckwith-wiedemann syndrome is characterized http://www.mercksource.com/pp/us/cns/cns_hc_children_content_adam.jspzQzpgzEzzSz

92. Beckwith-Wiedemann Syndrome   beckwithwiedemann syndrome. A rare, overgrowth disorder in which babies are large beckwith-wiedemann syndrome increases the risk of developing certain http://www.webref.org/cancer/b/beckwithwiedemann_syndrome.htm

Beckwith-Wiedemann syndrome Beckwith-Wiedemann syndrome A rare, overgrowth disorder in which babies are large at birth and may develop low blood sugar. Other common symptoms are a large tongue, large internal organs, and defects of the abdominal wall near the navel. Beckwith-Wiedemann syndrome increases the risk of developing certain cancers, especially Wilms’ tumor. Back Next Search! Cancer - A ... Tabularium™ WebRef™ Search WWW Search webref.org JourneyEd.com is the leading supplier of discounted software to students and faculty. This site hosted by EASY CGI Web Hosting

93. Large Muscles beckwithwiedemann syndrome l Cyclin-dependent kinase inhibitor 1C l Duplicationof chromosome 11p15.5; Dominant with incomplete penetrance http://www.neuro.wustl.edu/neuromuscular/mother/mlarge.html

Front Search Index Links ... Patient Info LARGE OR PROMINENT MUSCLES Drugs Endocrinopathy Focal enlargement Infections ... Storage disorders Amyloidosis: Enlarged tongue Overusage Neural Myokymia Neuromyotonia Isaac's Syndrome Schwartz-Jampel Exercise: Bodybuilding Spasticity with persistent muscle spasms Orthostatic tremor Myotonia Congenita Hyperkalemic Periodic Paralysis Paramyotonia congenita Proximal myotonic myopathy (PROMM) ... Rippling Muscle Syndrome Partial Denervation Focal : Radiculopathy; Nerve lesion Later-onset Spinal Muscular Atrophies Polyneuropathy: HMSN I II Endocrinopathy Hypothyroid ... Acromegaly Muscular Dystrophies Disorders Dystrophinopathies Limb-Girdle Muscular Dystrophy: Myopathy with abnormal merosin Congenital muscular dystrophy with Respiratory failure Features causing hypertrophy Infections Cysticercosis Trichinosis Schistosomiasis Drug treatment adrenergic agonists: Albuterol; Clenbuterol Androgenic steroids Glycogen Amyloid Fatty replacement of muscle Gangliosidoses Focal enlargement Extremities or Trunk Focal partial denervation Complex repetitive discharges or Myokymia Old polio Focal myokymia Focal myositis : Acute onset; Pain

94. Beckwith-Wiedemann Syndrome: Imprinting In Clusters Revisited -- Maher And Reik An imprinted gene p57Kip2 is mutated in beckwithwiedemann syndrome. Imprinting mutations in the beckwith-wiedemann syndrome suggested by an altered http://www.jci.org/cgi/content/full/105/3/247

QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Full Text (PDF) Submit a response Alert me when this article is cited ... Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Cited by other online articles PubMed PubMed Citation Articles by Maher, E. R. Articles by Reik, W. J Clin Invest, February 2000, Volume 105, Number 3, 247-252 Perspective Beckwith-Wiedemann syndrome: imprinting in clusters revisited Eamonn R. Maher and Wolf Reik Section of Medical and Molecular Genetics, Department of Paediatrics and Child Health, University of Birmingham, Birmingham B15 2TT, United Kingdom Laboratory of Developmental Genetics and Imprinting, The Babraham Institute, Cambridge CB2 4AT, United Kingdom Address correspondence to: Eamonn R. Maher, Section of Medical and Molecular Genetics, Department of Paediatrics and Child Health, University of Birmingham, The Medical School, Edgbaston, Birmingham B15 2TT, United Kingdom. Phone: 44-121-627-2630; Fax: 44-121-627-2618; E-mail: Introduction Genomic imprinting, a process that causes genes to be expressed

95. Beckwith Wiedemann, Syndrome : Sites Et Documents Francophones syndrome de beckwith-wiedemann, syndrome de Par Dr Gicquel C. http://www.chu-rouen.fr/ssf/pathol/beckwithwiedemannsyndrome.html

Beckwith Wiedemann, syndrome Définition [MeSH Scope Note ; traduction CISMeF] : Syndrome à défauts multiples caractérisé principalement par une hernie ombilicale (hernie ombelicale), une macroglossie, et un gigantisme et de façon secondaire par une viscéromégalie, une hypoglycémie, et des anomalies de l'oreille. Synonyme(s) CISMeF Beckwith Wiedemann ; Wiedemann-Beckwith, syndrome de ; omphalocèle-macroglossie-gigantisme . Arborescence(s) Beckwith Wiedemann, syndrome Beckwith-Wiedemann syndrome maladies et malformations congénitales, héréditaires et néonatales Position du mot-clé dans l' (les) arborescence(s) : Vous pouvez consulter toutes les ressources ou seulement les principales ou utiliser l' outil de recherche les recommandations les documents concernant l' enseignement les documents destinés aux patients Ou consulter ci-dessous une sélection des principales ressources : Qualificatifs : diagnostic patient Beckwith-Wiedemann, syndrome de [Par Dr Gicquel C. Site éditeur Orphanet base de données sur les maladies rares et les médicaments orphelins. Direction Générale de la Santé / INSERM ; signes de la maladie, sites internet, dysmorphologie, conseil génétique, hypertrophies hémifaciales, laboratoires de diagnostic, projets de recherche, associations de patients ; pays : France ; langue : français ; format : html ; accès : gratuit ; non parrainé ; daté de : 2001 ; visité le : 10/09/2003]. mots clés : *Beckwith Wiedemann, syndrome

96. Beckwith Wiedemann Syndrome Beckwith Wiedemann syndrome (BWS) is a rare genetic disorder. It may becharacterized by a wide spectrum http://my.webmd.com/hw/raising_a_family/nord52.asp

var guid_source = ""; var guid_source_id = ""; //unused var encodedurl = ""; WebMD Today Home WebMD News Center XML News via RSS Member Services WebMD University My WebMD Find a Physician Medical Info Check Symptoms Medical Library Health Tools Clinical Trials ... Women, Men, Lifestyle Who We Are About WebMD Site Map Health Topics Symptoms ... For a Complete Report Beckwith Wiedemann Syndrome Important It is possible that the main title of the report Beckwith Wiedemann Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms Beckwith-Syndrome BWS EMG Syndrome Exomphalos-Macroglossia-Gigantism Syndrome Hypoglycemia with Macroglossia Macroglossia-Omphalocele-Visceromegaly Syndrome Omphalocele-Visceromegaly-Macroglossia Syndrome Visceromegaly-Umbilical Hernia-Macroglossia Syndrome Wiedmann-Beckwith Syndrome Disorder Subdivisions None General Discussion Beckwith-Wiedemann syndrome (BWS) is a rare genetic disorder. It may be characterized by a wide spectrum of symptoms and findings that vary in range and severity from case to case. However, in many individuals with the syndrome, associated features may include above average weight and length at birth and/or increased growth after birth (postnatally); an unusually large tongue (macroglossia); enlargement of certain abdominal organs (visceromegaly); and/or abdominal wall defects. BWS may also be characterized by low blood sugar levels within the first days of life (neonatal hypoglycemia); advanced bone age, particularly up to age four; the presence of distinctive linear grooves in the ear lobes and/or other abnormalities of the facial area; and/or an increased risk of developing certain childhood cancers.

97. Beckwith Wiedemann Syndrome Complete online version of The Encyclopaedia of Medical Imaging including textand images from The Encyclopaedia of Medical Imaging s eight book volumes http://www.amershamhealth.com/medcyclopaedia/medical/Volume VII/BECKWITH WIEDEM

financial services our commitment our company Search Medcyclopaedia for: Search marked text (mark text before you click) Browse entry words starting with: A B C D ... amershamhealth.com Beckwith wiedemann syndrome, (John Bruce Beckwith, born1933, American pathologist; Hans Rudolf Wiedemann, born 1915, German paediatrician).The clinical features are macroglossia, visceromegaly, umbilical hernia and hypoglycaemia. There is an increased incidence of Wilms tumour . Ultrasound examination confirms the visceromegaly which mainly affects the kidneys and liver. The umbilical hernia is visible on plain abdominal radiographs.The associated neoplasms affect the kidneys and liver. DWP The Encyclopaedia of Medical Imaging Volume VII Corporate Products Financial Services Our Commitment ... Terms of Conditions

98. Beckwith Wiedemann Syndrome Complete online version of The Encyclopaedia of Medical Imaging including textand images from The Encyclopaedia of Medical Imaging s eight book volumes http://www.amershamhealth.com/medcyclopaedia/medical/Volume IV 2/BECKWITH WIEDE

financial services our commitment our company Search Medcyclopaedia for: Search marked text (mark text before you click) Browse entry words starting with: A B C D ... amershamhealth.com Beckwith wiedemann syndrome, see Beckwith Wiedemann syndrome and Beckwith Wiedemann syndrome renal manifestation HH The Encyclopaedia of Medical Imaging Volume IV 2 Corporate Products Financial Services Our Commitment ... Terms of Conditions

99. Beckwith Wiedemann Syndrome - St. Joseph Mercy, Ann Arbor Michigan Beckwith Wiedemann syndrome St. Joseph Mercy Health System Hospitals servingAnn Arbor, SE Michigan, Washtenaw County, Livingston County, Wayne County, http://www.sjmercyhealth.org/12661.cfm

@import url(default.css); Online Health Information Health Information - Rare Diseases and Disorders Back to Health Library Print This Page Email to a Friend National Organization for Rare Disorders, Inc. Beckwith Wiedemann Syndrome Synonyms Disorder Subdivisions General Discussion Resources ... For a Complete Report Important It is possible that the main title of the report Beckwith Wiedemann Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms Beckwith-Syndrome BWS EMG Syndrome Exomphalos-Macroglossia-Gigantism Syndrome Hypoglycemia with Macroglossia Macroglossia-Omphalocele-Visceromegaly Syndrome Omphalocele-Visceromegaly-Macroglossia Syndrome Visceromegaly-Umbilical Hernia-Macroglossia Syndrome Wiedmann-Beckwith Syndrome Disorder Subdivisions None General Discussion Beckwith-Wiedemann syndrome (BWS) is a rare genetic disorder. It may be characterized by a wide spectrum of symptoms and findings that vary in range and severity from case to case. However, in many individuals with the syndrome, associated features may include above average weight and length at birth and/or increased growth after birth (postnatally); an unusually large tongue (macroglossia); enlargement of certain abdominal organs (visceromegaly); and/or abdominal wall defects. BWS may also be characterized by low blood sugar levels within the first days of life (neonatal hypoglycemia); advanced bone age, particularly up to age four; the presence of distinctive linear grooves in the ear lobes and/or other abnormalities of the facial area; and/or an increased risk of developing certain childhood cancers.

100. Beckwith Wiedemann Syndrome: Link Found To Assisted Reproduction, December 19, 2 OBGYN.net Headline News page, daily womens health news. http://www.obgyn.net/newsheadlines/womens_health-Beckwith_Wiedemann_Syndrome-200

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