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Sequencing Progress
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All: 60 
OMIM dbSNP: 10 
OMIM UniSTS: 11 
Items 1 - 20 of 60
 
 of 3
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1: 208300 Links
ASCITES, CHYLOUS
2: %267000 Links
RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM
3: %265300 Links
LYMPHANGIECTASIA, PULMONARY, CONGENITAL; CPL
4: #603528 Links
DEHYDRATED HEREDITARY STOMATOCYTOSIS, PSEUDOHYPERKALEMIA, AND PERINATAL EDEMA
Gene map locus 16q23-q24
5: #256550 GeneTests, Links
NEURAMINIDASE DEFICIENCY
SIALIDOSIS, TYPE I, INCLUDED
Gene map locus 6p21.3
6: #269920 GeneTests, Links
INFANTILE SIALIC ACID STORAGE DISORDER
Gene map locus 6q14-q15
7: #261515 GeneTests, Links
D-BIFUNCTIONAL PROTEIN DEFICIENCY
Gene map locus 5q2, 3p23-p22
8: %194380 Links
DEHYDRATED HEREDITARY STOMATOCYTOSIS; DHS
Gene map locus 16q23-q24
9: %269860 GeneTests, Links
SHORT RIB-POLYDACTYLY SYNDROME, TYPE IV
10: 600461 Links
HEMOLYTIC ANEMIA, LETHAL CONGENITAL NONSPHEROCYTIC, WITH GENITAL AND OTHER ABNORMALITIES
11: 271500 Links
SPLENOPORTAL VASCULAR ANOMALIES
12: 256150 Links
NEPHROSIALIDOSIS
13: #251880 GeneTests, Links
MITOCHONDRIAL DNA DEPLETION SYNDROME, HEPATOCEREBRAL FORM
Gene map locus 2p23-p21, 16q22, 13q12.2-q13, 2p13
14: 240150 Links
HYPERVITAMINOSIS A, SUSCEPTIBILITY TO
15: #232500 GeneTests, Links
GLYCOGEN STORAGE DISEASE IV
GSD IV, CLASSIC HEPATIC, INCLUDED
Gene map locus 3p12
16: %226300 Links
ENTEROPATHY, PROTEIN-LOSING
17: #608115 Links
OVARIAN HYPERSTIMULATION SYNDROME
Gene map locus 2p21-p16
18: #607625 GeneTests, Links
NIEMANN-PICK DISEASE, TYPE C2
Gene map locus 14q24.3
19: %277320 Links
VISCERAL MYOPATHY, FAMILIAL, WITH EXTERNAL OPHTHALMOPLEGIA
20: +276700 GeneTests, Links
TYROSINEMIA, TYPE I
FUMARYLACETOACETATE HYDROLASE, INCLUDED; FAH, INCLUDED
Gene map locus 15q23-q25
Items 1 - 20 of 60
 
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Jun 21 2006 12:14:26