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All: 17 
OMIM dbSNP: 1 
OMIM UniSTS: 3 
Items 1 - 17 of 17
 One page.
1: #263200 GeneTests, Links
POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE; ARPKD
HEPATIC FIBROSIS, CONGENITAL, INCLUDED
Gene map locus 6p21.1-p12
2: %143400 Links
MULTICYSTIC RENAL DYSPLASIA, BILATERAL; MRD
Gene map locus 6p
3: 300404 Links
BRAIN ANOMALIES, RETARDATION, ECTODERMAL DYSPLASIA, SKELETAL MALFORMATIONS, HIRSCHSPRUNG DISEASE, EAR/EYE ANOMALIES, CLEFT PALATE/CRYPTORCHIDISM, AND KIDNEY DYSPLASIA/HYPOPLASIA
Gene map locus Chr.X
4: *607102 GeneTests, Links
WILMS TUMOR 1 GENE; WT1
Gene map locus 11p13
5: %191830 GeneTests, Links
UROGENITAL ADYSPLASIA, HEREDITARY
6: 600989 Links
INFUNDIBULOPELVIC DYSGENESIS
7: *601653 GeneTests, Links
EYES ABSENT 1; EYA1
Gene map locus 8q13.3
8: *189907 GeneTests, Links
TRANSCRIPTION FACTOR 2; TCF2
Gene map locus 17cen-q21.3
9: %164210 GeneTests, Links
HEMIFACIAL MICROSOMIA; HFM
Gene map locus 14q32
10: %211890 Links
CAMPOMELIA, CUMMING TYPE
11: %606170 Links
GENITOPATELLAR SYNDROME
12: %243910 GeneTests, Links
ARIMA SYNDROME
13: *590050 GeneTests, Links
TRANSFER RNA, MITOCHONDRIAL, LEUCINE, 1; MTTL1
14: #107480 GeneTests, Links
TOWNES-BROCKS SYNDROME; TBS
TOWNES-BROCKS-BRANCHIOOTORENAL-LIKE SYNDROME, INCLUDED
Gene map locus 16q12.1
15: 192350 GeneTests, Links
VATER ASSOCIATION
VACTERL ASSOCIATION, INCLUDED
16: #118450 GeneTests, Links
ALAGILLE SYNDROME 1; AGS1
Gene map locus 20p12
17: #312870 GeneTests, Links
SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1
Gene map locus Xq26
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Jun 21 2006 12:14:26