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All: 87 
OMIM dbSNP: 4 
OMIM UniSTS: 14 
Items 1 - 20 of 87
 
 of 5
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1: 182940 GeneTests, Links
SPINA BIFIDA
T/t LOCUS, POSSIBLE EQUIVALENT OF, INCLUDED
Gene map locus 1q43, 5p15.3-p15.2
2: 301410 GeneTests, Links
ANENCEPHALY--SPINA BIFIDA
3: 183802 Links
SPLIT-HAND WITH OBSTRUCTIVE UROPATHY, SPINA BIFIDA, AND DIAPHRAGMATIC DEFECTS
4: 300293 Links
SPINA BIFIDA, X-LINKED
5: *156570 Links
5-@METHYLTETRAHYDROFOLATE-HOMOCYSTEINE S-METHYLTRANSFERASE; MTR
Gene map locus 1q43
6: *158105 Links
CHEMOKINE, CC MOTIF, LIGAND 2; CCL2
CORONARY ARTERY DISEASE, MODIFIER OF, INCLUDED
Gene map locus 17q11.2-q12
7: *602568 GeneTests, Links
METHIONINE SYNTHASE REDUCTASE; MTRR
Gene map locus 5p15.3-p15.2
8: #161200 GeneTests, Links
NAIL-PATELLA SYNDROME; NPS
Gene map locus 9q34.1
9: 231970 Links
GLUTEAL MUSCLES, ABSENCE OF
10: +172460 Links
METHYLENETETRAHYDROFOLATE DEHYDROGENASE 1; MTHFD1
METHYLTETRAHYDROFOLATE CYCLOHYDROLASE DEFICIENCY, INCLUDED
Gene map locus 14q24
11: %206500 Links
ANENCEPHALY
12: *173490 Links
PLATELET-DERIVED GROWTH FACTOR RECEPTOR, ALPHA; PDGFRA
PDGFRA/BCR FUSION GENE, INCLUDED
Gene map locus 4q12
13: #193500 GeneTests, Links
WAARDENBURG SYNDROME, TYPE I; WS1
Gene map locus 2q35
14: 184300 Links
SPONDYLOSIS, CERVICAL
15: +104150 Links
ALPHA-FETOPROTEIN; AFP
ALPHA-FETOPROTEIN, HEREDITARY PERSISTENCE OF, INCLUDED; HPAFP, INCLUDED
Gene map locus 4q11-q13
16: 601635 GeneTests, Links
NEURAL TUBE DEFECT, FOLATE-RESISTANT
17: 601829 Links
ACROFACIAL DYSOSTOSIS, PALAGONIA TYPE
18: 600122 Links
MALE PSEUDOHERMAPHRODITISM/MENTAL RETARDATION SYNDROME, VERLOES TYPE
19: %311000 Links
OPHTHALMOPLEGIA, EXTERNAL, AND MYOPIA; OPEM
20: %305600 Links
FOCAL DERMAL HYPOPLASIA; DHOF
Items 1 - 20 of 87
 
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Jun 21 2006 12:14:26