61. Identification Of A Mutation In DLX3 Associated With Tricho-dento- Osseous (TDO) Several other clinical features, including macrocephaly, dolicocephaly, a highprevalence of dental caries, narrowing of the ear canal, altered craniofacial http://hmg.oxfordjournals.org/cgi/content/full/7/3/563

JOURNAL HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Abstract FREE Full Text (PDF) Alert me when this article is cited ... Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed ... Cited by other online articles Search for citing articles in: ISI Web of Science (66) Request Permissions PubMed PubMed Citation Articles by Price, J. A. Articles by Hart, T. C. Human Molecular Genetics Pages Identification of a mutation in associated with tricho-dento-osseous (TDO) syndrome Introduction Results Identification of a common haplotype in the TDO region Mapping of DLX7 to the common haplotype region and mutational analysis ... References Identification of a mutation in associated with tricho-dento-osseous (TDO) syndrome Jennifer A. Price Donald W. Bowden J. Tim Wright Mark J. Pettenati Thomas C.

62. Journal Of Pediatric Hematology Oncology - UserLogin After the skin edema subsided, he was noted to have facial features consistentwith NS, as evidenced by dolicocephaly, downward obliquity of the palpebral http://www.jpho-online.com/pt/re/jpho/fulltext.00043426-199911000-00015.htm

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63. The Nordish Portal Quote As for Normandy and dolicocephaly, it is not all as rare as you mightthink. If I can dig up the approximation I will post them. http://www.nordish.net/forum/showthread.php?t=1119&page=2

64. Science - Ethics - Power, Turner Statement Regarding Eugenics significant correlations could be established between dolicocephaly andmesocephaly or variations in cephalic index and reproductive performance. http://www.umich.edu/~idpah/SEP/sep_te.html

EUGENIC IDEAS IN JAMES NEEL'S CONCEPTION OF "PRIMITIVE SOCIETY" Terence Turner Department of Anthropology, Cornell University November 10, 2000 A puzzling feature of the outpouring of messages and testimonials in support of James Neel against the allegations about his actions and ideas in Patrick Tierney's book, Darkness in El Dorado, is the denial that Neel held eugenic beliefs. In his discussions of primitive society, Neel was quite explicit about his eugenic ideas, both in print and in conversation. They have a fundamental place in his conception of the selective advantages of primitive (and specifically Yanomama) social organization. These ideas are most fully expounded in his article, "On being Headman". I quote at length from this article. I have put certain passages in upper case for emphasis (page numbers are indicated in brackets). [p.285-] Some genetic implications of [Yanomami] culture Some caveats Are there tenable countermeasures to the loss of our primitive population structure? Menu of Resources Doctoral Program in Anthropology and History

65. 3802cr5 More recently in 1992, Phelan et al reported a threeyear-old with developmentaldelay, hypotonia, dolicocephaly, ptosis, epicanthal folds and posteriorly http://www.sma.org.sg/smj/3802/articles/3802cr5.htm

Journals Present Issue Past Issues THESMANEWS Present Issue Past Issues SMJ Editorial Board Letters to the Editor S I N G A P O R E M E D I C A L J O U R N A L This site is supported by Health ONE Partial Monosomy For Chromosome 22 In A Girl With Mental Retardation Y P Yong, L A Knight, M H Yong, S Lam, L Y Ho ABSTRACT This report describes a 5-year 6-month-old Chinese girl with partial monosomy for the long arm of chromosome 22. The karyotype was 46,XX / 46,XX,del (22) (ql3.2). She presented with global developmental delay. Clinical features include seizures, failure-to-thrive, prominent ears, long philtrum and abnormal skin pigmentation on the face and limbs. Keywords: mental retardation, partial monosomy 22 INTRODUCTION Mental retardation in association with physical abnormalities is highly suggestive of chromosomal aberrations. With the availability of increasingly sophisticated techniques in the field of cytogenetics, more patients with so-called idiopathic mental retardation and minor dysmorphic facial features may in reality have an abnormal chromosome karyotype previously undetected. Therefore, mental retardation attributed to chromosomal abnormality will be better defined with increasing awareness and reporting. CASE REPORT Psychological assessment at age 2 years 11 months confirmed global developmental delay with a functional age of approximately 15 months (Bayley’s Scale of Infant development). Subsequent assessment at age 4 years 1 month showed her functioning profile to be about 17 months and speech and language skills at about 12 months.

66. Genetica Medica - Università Degli Studi Di Siena - XLinked Mental Retardation mild mental retardation, dolicocephaly; plagiocephaly;squint;high vaulted and narrow palate; tended upper lip; clinosactyly of fifth......Trait http://xlmr.unisi.it/dettagli2.asp?Cod=105

67. Sci.anthropology.paleo: Re: Homo Heidelbergensis toes longer than first toes (well, mine are), relative dolicocephaly (at leastamongst early populations, it seems to have diminished in the last http://www.anatomy.usyd.edu.au/danny/anthropology/sci.anthropology.paleo/archive

Re: Homo heidelbergensis Ken Brown ( rkjb@cix.compulink.co.uk Mon, 30 May 1994 23:21:50 +0000 Messages sorted by: [ date ] [ thread ] [ subject ] [ author ] Next message: R.Downing: "Re: African Eve" Maybe in reply to: NICHOLLS PHILIP A: "Homo heidelbergensis" Next in thread: Ethan Vishniac: "Re: Homo heidelbergensis" sarima@netcom.com (Stanley Friesen) wrote: eh? What evidence is there that Jews are or ever were a seperate breeding community from anybody else? There are of course well-known genes whose frequency differs between Jewish closely related to Gentiles living nearby than to remote Jewish populations. said to look just like other Indians. And so on. Back on topic for a while - I have a purely sentimental attraction to the idea that some of the oddities about us northern Europeans are due to Partial albinism, vestigal brow ridges (I can feel mine distinctly), second toes longer than first toes (well, mine are), relative dolicocephaly (at least amongst early populations, it seems to have diminished in the last millenium)... until someone proves the contrary with genetic evidence I shall

68. Sci.anthropology.paleo: Re: Homo Heidelbergensis toes longer than first toes (well, mine are), relativedolicocephaly (at ^^^^^^^^^^^^^^^^^^^^^^^^^^^^ least amongst early populations,it seems to have http://www.anatomy.usyd.edu.au/danny/anthropology/sci.anthropology.paleo/archive

Re: Homo heidelbergensis Xiaoguang Zhang ( zhang@gmsds.ms.ornl.gov Sun, 5 Jun 1994 21:01:30 GMT Messages sorted by: [ date ] [ thread ] [ subject ] [ author ] Next message: Cameron Laird: "Re: aquatic ape?" Previous message: Stanley Friesen: "Re: Early diets" Maybe in reply to: NICHOLLS PHILIP A: "Homo heidelbergensis" Ken Brown (rkjb@cix.compulink.co.uk) wrote: : Back on topic for a while - I have a purely sentimental attraction to the : idea that some of the oddities about us northern Europeans are due to : Partial albinism, vestigal brow ridges (I can feel mine distinctly), second : toes longer than first toes (well, mine are), relative dolicocephaly (at : least amongst early populations, it seems to have diminished in the last : millenium)... until someone proves the contrary with genetic evidence I shall : persist in imagining that I have a few Neanderthal ancestors! I wonder if this constitutes counter argument: I'm a Chinese, and my second toes are longer than first toes. Same for my wife (also a Chinese). Does that mean that I too have a few Neanderthal ancestors?

69. The World Diseases A 2 Z Names By Countrylinks And Dr Impex dolicocephaly. Down Syndrome. Drooling. Dry Eye. Dubowitz Syndrome. Dwarfism.Dysencephalia Splanchnocystica. Dysmenorrhea. Dyspareunia. Dysphagia http://www.countrylinks.biz/diseases.htm

Country Links Dr Impex free on-line Services Note: search with CTRL + F A Aarskog Syndrome Aase Syndrome Abetalipoproteinemia Ablepharon-Macrostomia Syndrome Achilles Tendonitis Achondroplasia Acoustic Neuroma Acromegaly Activated Protein C Resistance Acute Idiopathic Polyneuritis ADD and ADHD Addiction and Recovery Addison's Disease Adiposis Dolorosa Adjustment Disorders Adrenoleukodystrophy Agnosia Agoraphobia Aicardi Syndrome AIDS Alagille Syndrome Albinism Alcoholism Alexander Disease Alkaptonuria Allergies Alopecia Alpers' Disease Alpha1 Antitrypsin Deficiency Alport Syndrome Alstrom Syndrome Alternating Hemiplegia Altophobia Alzheimer's Amblyopia Amputee Amyloidosis Amyoplasia Congenita Amyotrophic Lateral Sclerosis Anal Fissures Anemia Anencephaly Aneurysm Angina Pectoris Anophthalmos Anorexia Anosmia Anterior Knee Pain Syndrome Antiphospholipid Syndrome Anxiety Aortic Valve Disease Apert Syndrome Aphasia Aplastic Anemia Apnea, Sleep Appendicitis Arrhythmia Arteriohepatic Dysplasia Arthritis Arthrogryposis Asbestosis Asperger's Syndrome Aspergillosis Asthma Atherosclerosis Athlete's Foot Atrial Fibrillation Attachment Disorder Attention Deficit Disorder Autism Auto Immune Disorders Aviophobia Aviatophobia B Bacillary Angiomatosis Back Disorders Bad Breath Balanitis Baldness Barth Syndrome Bassen Kornzweig Syndrome Batten Disease Beckwith-Wiedemann Syndrome Behcet's Syndrome Bell's Palsy Benign Breast Lumps Benign Prostatic Hyperplasia Berger's Disease Beriberi Beryllium Disease

70. Phelan-McDermidin Oireyhtymä - Kehitysvammahuollon Tietopankki Kasvonpiirteisiin kuuluu pitkäpäisyys (dolicocephaly), täyteläiset kulmakarvat,silmien paksut riippuluomet, pitkät silmäripset, leveä nenänsilta, http://www.saunalahti.fi/kup/syndroma/phelan_mcdermid.htm

Kehitysvammahuollon tietopankki Velttous, puuttuva puhe, kokonaisvaltainen kehitysviive ja normaali tai kiihtynyt kasvu Phelan-McDermidin oireyhtymä Deleetio 22q13-syndrooma Mary C. Phelan kirjoitti Orphanet -artikkelissaan (2003), että oireyhtymää luonnehtii vastasyntyneen velttous, kokonaisvaltainen kehityksen viivästyminen, normaali tai kiihtynyt kasvu, puuttuva tai vaikeasti viivästynyt puhe ja pienet epämuodostumat. Kasvonpiirteisiin kuuluu pitkäpäisyys ( dolicocephaly ), täyteläiset kulmakarvat, silmien paksut riippuluomet, pitkät silmäripset, leveä nenänsilta, litteät keskikasvot, täyteläiset posket, sipulimainen nenä, suuret tai epätavalliset korvat ja kärjekäs leuka. Muita piirteitä olivat olleet suuret kädet, vajaakasvuiset varpaankynnet, puutteellinen hieneritys ja ristiluun kuoppa ( sacral dimple ). Käyttäytymistä kuvattiin autistiseksi , mihin liittyi korkea kipukynnys ja piintynyt pureskelu tai tyhjä puhe. Kromosomin 22 pitkän varren loppupäästä (geenikarttamerkintä 22q13.3) puuttui perimäainesta. Deleetio oli osoittautunut niin pieneksi, että sitä oli vaikea havaita rutiininomaisissa kromosomitutkimuksissa. Yli 30%:lle vammautuneista oli pitänyt kahdesti tai useammin kromosomitutkimus ennen kuin poikkeavuus oli löytynyt. Phelan piti oireyhtymää alidiagnosoituna, koska sitä oli niin vaikea todentaa. Oireyhtymän piirteet olivat vaikuttaneet syntymähetkellä lieviltä. Suurella osalla

71. What Is Phelan-McDermid Syndrome? Facial features are fairly subtle and may not be recognized by your doctor longhead shape (dolicocephaly), puffiness around the eyes, long eyelashes, http://www.22q13.org/tell_me_more/2tmm_what_is_22q13.html

There is a wide range of severity of symptoms observed in people with the deletion, but most exhibit moderate to severe developmental delays, physically and intellectually, but especially in speaking and communicating. Very low muscle tone is a common trait of the syndrome, and many have problems with eating, sleeping and emotional stability. There are nearly 200 diagnosed cases of this deletion worldwide, but the large majority of these are small children due to the recent (1998) development of a reliable test for the deletion, so the actual number of people with the deletion is certainly much larger. Outreach to find and help these families with older children is one of the objectives of the support group. Most, but not all, children with this syndrome will have a number of characteristic features: Newborns usually have floppy muscle tone (hypotonia). Delayed in sitting up, rolling over, crawling and walking. Delayed or absent speech. Normal growth or may be tall for age.

72. Phelan-McDermid Syndrome Medical | Characteristics Prominent, poorly formed ears, 65 percent. Pointed chin, 62 percent.dolicocephaly (elongated head), 57 percent. Ptosis (droopy eyelids), 57 percent http://www.22q13.org/medical/characteristics.html

introduction basic chromosome facts testing for 22q13 ... medical glossary There is not as much specific data on the behavior aspects of individuals with deletion 22q13 as there is in other areas. Many of the behaviors listed below were brought up in parent sharing sessions. One parent would explain a particular behavior and many others would say they have observed it with their child too. Due to this there is only one behavior with a known percentage showing what portion of the deletion population exhibit it. Some behavioral characteristics: Teeth grinding Tongue thrusting Hair pulling Aversion to clothes Dr. Desmond Kelly compiled this list of attributes also saying many children outgrow the behaviors. Avoidance Strategies: Show anxiety in social situations Flap arms and hands/ repetitive movements Scream when excited Self stimulatory behavior, rocking Bite themselves Enjoy TV, music, movies that are repetitive Some of these behaviors can be regarded as possible adaptations to physical abnormalities these individuals face. Many children with this deletion have vision issues causing them to rely on their peripheral vision. This would in turn translate to not looking people in the eye, when in reality they might be looking at people using their peripheral vision because that is the easiest way for them to see. Finally, individuals with deletions 22q13 are able to express a wide range of emotions including joy, happiness, and love.

73. Disorders Of Cholesterol Biosynthesis -- Clayton 78 (2): 185 -- Archives Of Dise The dysmorphic features which have been described include microcephaly, dolicocephaly,a large fontanelle, a triangular facies with down slanted eyes and http://adc.bmjjournals.com/cgi/content/full/78/2/185

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS Author Keyword(s) Vol Page [Advanced] This Article Extract Full Text (PDF) Submit a response ... Citation Map Services Email this link to a friend Similar articles in ADC Online Similar articles in PubMed Alert me to new issues of the journal ... Cited by other online articles PubMed PubMed Citation Articles by Clayton, P. T Arch Dis Child 185-189 ( February ) Current topic Disorders of cholesterol biosynthesis Peter T Clayton Biochemistry Unit, Institute of Child Health and Metabolic Unit, Great Ormond Street Hospital for Children, London Correspondence to: Dr Peter T Clayton, Biochemistry Unit, Institute of Child Health, 30 Guilford Street, London WC1N 1EH. Functions of cholesterol Top Functions of cholesterol Sources of cholesterol Biosynthesis of cholesterol Disorders affecting the... Disorders affecting the...

74. OBGYN.net - OBGYN.net Ultrasound - Case Of The Month: SONOGRAPHIC FEATURES OF TR dolicocephaly, Prominent Cisterna Magna, Bicuspid Outflow Tract Valves.Cerebellar Hypoplasia, Single Umbilical Artery. Meningomyelocele http://www.obgyn.net/us/us.asp?page=/us/cotm/9905/cotm_9905

75. Dysostosis Multiplex Congenita - General Practice Notebook dolicocephaly; spatulate ribs oar-like; wide diaphyses and narrow epiphyses;wide metacarpals, phlanges, metatarsals - bullet-like; hypoplastic acetabulae http://www.gpnotebook.co.uk/cache/-831848417.htm

dysostosis multiplex congenita Dysostosis multiplex congenita is a radiological finding of a number of related features, including: dolicocephaly spatulate ribs - oar-like wide diaphyses and narrow epiphyses wide metacarpals, phlanges, metatarsals - bullet-like hypoplastic acetabulae kyphoscoliosis platyvertebrae ossification defects of the lower vertebral bodies Click here for more information...

76. Clinical Dysmorphology - UserLogin Other less common features include dolicocephaly, dysplastic ears, pointed chin,ptosis, epicanthic folds, saddle nose, fleshy hands, dysplastic toenails, http://www.clindysmorphol.com/pt/re/mcd/fulltext.00019605-200407000-00014.htm

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77. Is Three-dimensional Ultrasound Adding New For Detection Of Congenital Anomalies dolicocephaly. 34. 3. Anencephaly; hydramnios. 2932. 2. Occipitalencephalocele (twin). 24,26. 1. Hygroma colli; oligohydramnios http://www.gfmer.ch/International_activities_En/El_Mowafi/Three-dimensional_ultr

Diaa M. El-Mowafi - Zagagig University, Egypt Is three-dimensional ultrasound adding new for detection of congenital anomalies? Diaa M. El-Mowafi MD Associate Professor, Department of Obstetrics and Gynecology, Benha Faculty of Medicine, Egypt Fellow, Geneva University, Switzerland Abstract Objective: to evaluate the three-dimensional ultrasound (3D US) as a recent method for detection of fetal congenital anomalies in comparison with the traditional 2 D US. Materials and Methods: Thirty-eight fetuses had been examined with the same equipment containing the traditional 2D US and 3D US. Each fetus had been scanned with one volume probe that has the 2 options; 2D and 3D US. The gestational ages of the examined fetuses were 22-36 weeks. Results: Seventy-two abnormalities were detected with 2D US, real-time 3D US, or both in 38 fetuses. Of the 72 fetal abnormalities, sixteen (22%) that had not been identified adequately at 2D US were disclosed with real-time 3D US. For eighteen abnormalities (25%) diagnosed at 2D US, real-time 3D US gave further information. Thirty-eight abnormalities (53%) were diagnosed only with 2D US. Conclusion: Real-time 3D US is useful for evaluating fetal abnormalities as a supplement to 2D US, particularly for abnormalities of the face, head, fingers, and skeleton, but real-time 3D US is unlikely to be helpful for detecting intra-fetal abnormalities except for skeletal abnormalities and some pathologic changes with fluid accumulation.

78. Centronuclear And Myotubular Myopathy Information Point Patients often have typical myopathic facies with dolicocephaly, a high forehead,long face with midface hypoplasia and a narrow higharched palate with http://tonilouise.tripod.com/cnmgailreport2003.html

setAdGroup('67.18.104.18'); var cm_role = "live" var cm_host = "tripod.lycos.com" var cm_taxid = "/memberembedded" Search: Lycos Tripod 40 Yr Old Virgin Share This Page Report Abuse Edit your Site ... Next CENTRONUCLEAR AND MYOTUBULAR MYOPATHY INFORMATION POINT United Kingdom Established March 2001 The adverts above help to keep this site free; please feel free to visit these sites but note that I do not endorse them in any way - pop-ups can be eliminated by downloading the Google toolbar powered by bravenet.com Powered by Bravenet.com Welcome What's New? About the Condition ... In Memory Ways to Help Make a Donation Participate in Research Interactive Elements Got something to share? Add it to the Notice Board It's Good to Talk ... Acknowledgements Links to Other Sites (move mouse over pictures and click) more Links ...... Toni's Website Since 17th August 2003 Spotted An Error I've Missed? Please drop me a quick email so that I can correct the error and improve the site for others - Thank you TEXT size too BIG or too small for your computer? Click on View , click on Text Size and adjust accordingly Centronuclear / Myotubular Myopathy A Report Authors: Gail Herman, MD, PhD; Soma Das, PhD - December 2001

79. PEDIATRICS scaphocephaly=dolicocephaly premature closure of the sagital suture. brachicoronal. trigonal metopic. occicephaly lambdoid http://radiologynotes.servehttp.com/peds/pediatrics.htm

80. BigTome.com Rhinitis Retinitis Pigmentosa Cyrptococcosis Gastrointestinal Disorders MurmursPeripheral Neuropathy Hidradenitis Suppurativa dolicocephaly SteinLeventhal http://disease.bigtome.com/bth/bt1_disease_1.shtml

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