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Association of Single Nucleotide Polymorphisms on Locus 18q21.1 in the Etiology of Nonsyndromic Cleft Lip Palate (NSCLP) in Indian Multiplex Families

Background  Cleft lip palate (CLP) is a common congenital anomaly with multifactorial etiology. Many polymorphisms at different loci on multiple chromosomes were reported to be involved in its etiology. Genetic research on a single multigenerational American family reported 18q21.1 locus as a high-r...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:Glob Med Genet
Päätekijät: Neela, Praveen Kumar, Reddy, Gosla Srinivas, Husain, Akhter, Mohan, Vasavi, Thumoju, Sravya, BV, Rajeshwari
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Georg Thieme Verlag KG 2021
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7964250/
https://ncbi.nlm.nih.gov/pubmed/33748821
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0041-1723087
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