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All: 56 
OMIM dbSNP: 8 
OMIM UniSTS: 13 
Items 1 - 20 of 56
 
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1: 213820 Links
CEREBRAL MALFORMATION, SEIZURES, HYPERTRICHOSIS, AND OVERLAPPING FINGERS
2: #304120 GeneTests, Links
OTOPALATODIGITAL SYNDROME, TYPE II; OPD2
Gene map locus Xq28, Xq28
3: %108145 GeneTests, Links
ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5
4: #108120 GeneTests, Links
ARTHROGRYPOSIS, DISTAL, TYPE 1; DA1
Gene map locus 9p13.2-p13.1
5: 601016 Links
MIDLINE MALFORMATIONS, MULTIPLE, WITH LIMB ABNORMALITIES AND HYPOPITUITARISM
6: #309580 Links
MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED
Gene map locus Xq13
7: #606056 GeneTests, Links
GLUCOSIDASE I DEFICIENCY
Gene map locus 2p13-p12
8: *300075 GeneTests, Links
RIBOSOMAL PROTEIN S6 KINASE, 90-KD, 3; RPS6KA3
MENTAL RETARDATION, X-LINKED 19, INCLUDED; MRX19, INCLUDED
Gene map locus Xp22.2-p22.1
9: #101400 GeneTests, Links
SAETHRE-CHOTZEN SYNDROME; SCS
SAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED
Gene map locus 10q26, 7p21
10: #604841 GeneTests, Links
STICKLER SYNDROME, TYPE II; STL2
Gene map locus 1p21
11: 606851 Links
CREE MENTAL RETARDATION SYNDROME
12: #601680 GeneTests, Links
ARTHROGRYPOSIS, DISTAL, TYPE 2B; DA2B
Gene map locus 17p13.1, 11p15.5, 11p15.5
13: #101600 GeneTests, Links
PFEIFFER SYNDROME
NOACK SYNDROME, INCLUDED
Gene map locus 10q26, 8p11.2-p11.1
14: #309000 GeneTests, Links
LOWE OCULOCEREBRORENAL SYNDROME; OCRL
Gene map locus Xq26.1
15: #175700 GeneTests, Links
GREIG CEPHALOPOLYSYNDACTYLY SYNDROME; GCPS
Gene map locus 7p13
16: #101200 GeneTests, Links
APERT SYNDROME
APERT-CROUZON DISEASE, INCLUDED
Gene map locus 10q26
17: *176943 GeneTests, Links
FIBROBLAST GROWTH FACTOR RECEPTOR 2; FGFR2
KERATINOCYTE GROWTH FACTOR RECEPTOR, INCLUDED; KGFR, INCLUDED
Gene map locus 10q26
18: 174100 Links
POLYDACTYLY, IMPERFORATE ANUS, AND VERTEBRAL ANOMALIES
19: *165240 GeneTests, Links
GLI-KRUPPEL FAMILY MEMBER 3; GLI3
Gene map locus 7p13
20: #153480 GeneTests, Links
MACROCEPHALY, MULTIPLE LIPOMAS, AND HEMANGIOMATA
Gene map locus 10q23.31
Items 1 - 20 of 56
 
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Jun 21 2006 12:14:26