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1.
Further evidence for a maternal genetic effect and a sex-influenced effect contributing to risk for human neural tube defects.
Birth Defects Res A Clin Mol Teratol
; 82(10): 662-9, 2008 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-18937341
2.
Refinement of 2q and 7p loci in a large multiplex NTD family.
Birth Defects Res A Clin Mol Teratol
; 82(6): 441-52, 2008 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-18452155
3.
Neural tube defects and folate pathway genes: family-based association tests of gene-gene and gene-environment interactions.
Environ Health Perspect
; 114(10): 1547-52, 2006 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-17035141
4.
High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35.
Birth Defects Res A Clin Mol Teratol
; 76(6): 499-505, 2006 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-16933213
5.
Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15.
Am J Med Genet A
; 140(24): 2776-85, 2006 Dec 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-17103432
6.
Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2.
Birth Defects Res A Clin Mol Teratol
; 73(11): 868-75, 2005 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-16237707
7.
SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects.
Hum Genet
; 117(2-3): 133-42, 2005 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-15883837
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