81. NewWorldOdour: List They were born without eyes (anophthalmos), ears, had missing organs, In babies born in Iraq in 2002, the incidence of anophthalmos was 250000 times http://changelog.newworldodour.co.uk/entries/page/102

prev next edward Bush will win the November 2004 election Fri 24th Sep 2004, 14:59 link George. W. Bush will win the USA November 2004 election. He will win, not because a majority of people will vote for him, but because he controls the voting system It's been demonstrated that the Diebold voting software is utterly insecure. Votes can be changed without anyone knowing, including the officials who run the election, The voting software has a backdoor that allows this easy manipulation of votes, but in a way that passes all spotchecks and verifications. According to internal Diebold memos, this backdoor appeared just after embezzler Jeffrey Dean became the senior programmer. Prior to working at Diebold, Dean was convicted of 23 counts of embezzlement which he admitted to commiting due to being blackmailed over killing someone in a fight (!). This software, complete with Dean's backdoors, has been in use in elections for over four years. It was used in November 2000, where Bush famously stole that election, and it will be used again this year. Appeals to the use of the software, or to implement measures preventing the kind of known backdoors are all being refused. The independant observation process

82. Anophthalmia And Microphthalmia Resource Guide [NEI Health Information] anophthalmos and microphthalmos, small eye syndrome. Provides information onanophthalmos and orbital implants, blepharospasm, ptosis and other eyelid http://www.nei.nih.gov/health/anoph/index.asp

Text size: S M L Health Funding News Laboratories ... Health Information Anophthalmia and Microphthalmia Related Topics: To order Anophthalmia and Microphthalmia Resource Guide visit our online catalog New! Diagram of the Eye Vision-Related TermsSelected Online Sources Finding an Eye Care Professional Talking to Your Doctor ... Eye Health Organizations Database New! On this page: Other Names What are anophthalmia and microphthalmia? What causes anophthalmia and microphthalmia? Can anophthalmia and microphthalmia be treated? ... Medical Literature The information provided in this Resource Guide was developed by the National Eye Institute to help patients and their families in searching for general information about anophthalmia and microphthalmia . An eye care professional who has examined the patient's eyes and is familiar with his or her medical history is the best person to answer specific questions. Other Names Anophthalmos and microphthalmos, small eye syndrome. What are anophthalmia and microphthalmia? Anophthalmia and microphthalmia are often used interchangeably. Microphthalmia is a disorder in which one or both eyes are abnormally small, while anophthalmia is the absence of one or both eyes. These rare disorders develop during pregnancy and can be associated with other birth defects. What causes anophthalmia and microphthalmia?

83. Your Right Hand Thief Some were born without eyes (anophthalmos), ears, with missing organs, In babies born in 2002, the incidence of anophthalmos was 250000 times greater http://righthandthief.blogspot.com/2005_06_05_righthandthief_archive.html

@import url(http://www.blogger.com/css/navbar/main.css); @import url(http://www.blogger.com/css/navbar/4.css); Notify Blogger about objectionable content. What does this mean? BlogThis! Your Right Hand Thief Laughing off hard truths in New Orleans They all ask'd for you kingfish Talking Points Memo Informed Comment Political Animal Body and Soul ... Kos pelicans Not Right Yatpundit realitique sssssturtle ... New Orleans Metblog daily pearls YRHT MAIN America An Eye Opener Angry Bear ... Zac Attack bivalves An old soul... Approximately Perfect Arvin Hill Bacon's Bits ... yer mom an' dem nutria Wizbang! the key monk PawPaw's House news The Dead Pelican NO Bulletin Pelican File lagniappe Appetites shoerants Go Fug Yourself have a snake ... Emerald Bile seasoned contact oyster stoa incorporate truth nobly act laugh and inspire Friday, June 10, 2005 Applause Congratulations to the Louisiana House and Senate for unanimously(!) approving HB 570 , which guarantees depleted uranium screenings as a medical benefit to war veterans. (Federal subsidies cover the cost of the tests.) As the Louisiana Weekly noted

84. Cancer Information, Research, And Treatment For All Types Of Cancer | OncoLink of retinoblastoma metastases for the mandible. 13q deletion syndrome associatedwith retinoblastoma and clinical anophthalmos of the opposite eye. http://www.oncolink.com/types/article.cfm?c=14&s=52&ss=416&id=7581

85. Eye Abnormalities anophthalmos. Search PUBMED for anophthalmos All Review Therapy Diagnosis.Blepharophimosis. Search PUBMED for Blepharophimosis http://medir.ohsu.edu/cliniweb/C11/C11.250.html

Eye Abnormalities Back to previous level Aniridia [1 more specific term/s, more link/s] Search PUBMED for Aniridia: All Review Therapy Diagnosis ... PAIRED BOX HOMEOTIC GENE 6; PAX6 Anophthalmos Search PUBMED for Anophthalmos: All Review Therapy Diagnosis Blepharophimosis Search PUBMED for Blepharophimosis: All Review Therapy Diagnosis Coloboma Search PUBMED for Coloboma: All Review Therapy Diagnosis Ectopia Lentis Search PUBMED for Ectopia Lentis: All Review Therapy Diagnosis Hydrophthalmos Search PUBMED for Hydrophthalmos: All Review Therapy Diagnosis Microphthalmos Search PUBMED for Microphthalmos: All Review Therapy Diagnosis ... MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS Retinal Dysplasia Search PUBMED for Retinal Dysplasia: All Review Therapy Diagnosis

86. Human Protein: P48431 - Transcription Factor SOX-2. EMBL Bioinformatic Harvester Disease, defects in sox2 are a cause of true or primary anophthalmos anophthalmos is a developmental defect characterized by complete absence of the http://harvester.embl.de/harvester/P484/P48431.htm

Human protein: P48431 - Transcription factor SOX-2. EMBL FORUM Length: 317 aa , molecular weight: 34310 Da , CRC64 checksum: MYNMMETELK PPGPQQTSGG GGGNSTAAAA GGNQKNSPDR VKRPMNAFMV WSRGQRRKMA 60 QENPKMHNSE ISKRLGAEWK LLSETEKRPF IDEAKRLRAL HMKEHPDYKY RPRRKTKTLM 120 KKDKYTLPGG LLAPGGNSMA SGVGVGAGLG AGVNQRMDSY AHMNGWSNGS YSMMQDQLGY 180 PQHPGLNAHG AAQMQPMHRY DVSALQYNSM TSSQTYMNGS PTYSMSYSQQ GTPGMALGSM 240 GSVVKSEASS SPPVVTSSSH SRAPCQAGDL RDMISMYLPG AEVPEPAAPS RLHMSQHYQS 300 GPVPGTAING TLPLSHM 317 // SOURCE BLAST OMIM SMART ... GoTo: SOURCE @ Stanford University SRY (sex determining region Y)-box 2 UniGene LocusLink OMIM GenAtlas ... Genome Browser Aliases SRY-BOX 2 SRY-RELATED HMG-BOX GENE 2 Chromosomal Location Chromosome/Cytoband Microarray Gene Expression Data Data available Show Gene Expression Data LocusLink Information Locus Link Summary This intronless gene encodes a member of the SRY-related HMG-box (SOX) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The encoded protein may act as a transcriptional activator after forming a protein complex with other proteins. Mutations in this gene have been associated with bilateral anophthalmia, a severe form of structural eye malformation. This gene lies within an intron of another gene called SOX2 overlapping transcript (SOX2OT). SwissProt Information SwissProt Accession No.

87. Microphthalmia Base de données sur les maladies rares et les médicaments orphelins. http://www.orpha.net/static/GB/microphthalmia.html

Orphanet database access Microphthalmia Direct access to data Update : 04/09/2005 Orphanet database access Orphanet database access Microphthalmia, Lenz type Direct access to data Summary Lenz's micropthalmos is an X-linked inherited syndrome characterized by coloboma, microphthalmia (97% of cases) and cataract, or sometimes anophthalmia. Other associated signs include skeletal and/or digital abnormalities (97%) affecting the clavicles and thumbs (clinodactily), mental retardation and growth disorders (66%), microcephaly (55%), detached ears (53%), hollow palate and dental abnormalities (45%), renal hypoplasia (37%), cryptorchidism (34%), and congenital cardiopathy (8%). Each disorder must be treated specifically. *Author: O. Roche, M.D. (July 2005)* Clinical signs Microphthalmos X-linked recessive inheritance Abnormal dental position Long/large ear Mental retardation(mild) Microcephaly Preauricular pits Preauricular tags Tooth shape anomaly Clavicle absent/abnormal Cleft palate Clinodactyly of fifth finger Clinodactyly of toes Congenital cardiac anomaly Ectopic/horseshoe/fused kidneys High vaulted/narrow palate Hypospadias/epispadias Increased body hair Kiphosis Late eruption of teeth Sacral sinus/dimple Scoliosis Short stature/dwarfism Simian crease Speech defect Squint/paresis of ocular muscles Syndactyly of toes Undescended/ectopic testes Ureteric anomalies(reflux/duplex system) Webbed neck Update : 04/09/2005 Orphanet database access

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