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1.
Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only.
Hum Mol Genet
; 26(4): 829-842, 2017 02 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-28087736
2.
Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate.
Am J Hum Genet
; 98(4): 755-62, 2016 Apr 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-27018475
3.
Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene.
PLoS Genet
; 12(3): e1005914, 2016 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-26968009
4.
Replication analysis of 15 susceptibility loci for nonsyndromic cleft lip with or without cleft palate in an italian population.
Birth Defects Res A Clin Mol Teratol
; 106(2): 81-7, 2016 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-26648166
5.
Further evidence for deletions in 7p14.1 contributing to nonsyndromic cleft lip with or without cleft palate.
Birth Defects Res A Clin Mol Teratol
; 106(9): 767-72, 2016 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-27384521
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