Výsledky vyhledávání - "N, Naili Muhamad Nor"

De Novo Interstitial Deletion of 1q32.2–q32.3 Including the Entire IRF6 Gene in a Patient with Oral Cleft and Other Dysmorphic Features

Autor: Wan Azman Wan Sulaiman, Raja Noriza Raja Ariffin, Ahmad Sukari Halim, N. Naili Muhamad Nor, Iman Salahshourifar, Bin Alwi Zilfalil

Publikováno v: Cytogenetic and Genome Research. 134:83-87

Background: Microdeletion of the Van der Woude syndrome (VWS) critical region is a relatively rare event, and only a few cases have been reported in the medical literature. The extent of the deletion and the genotype-phenotype correlation are 2 cruci

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::82c24737c524b3f21929d167f73c178e
https://doi.org/10.1159/000325541

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De novo interstitial deletion of 1q32.2-q32.3 including the entire IRF6 gene in a patient with oral cleft and other dysmorphic features

Autor: I, Salahshourifar, A S, Halim, W A W, Sulaiman, R, Ariffin, N, Naili Muhamad Nor, B A, Zilfalil

Publikováno v: Cytogenetic and genome research. 134(2)

Microdeletion of the Van der Woude syndrome (VWS) critical region is a relatively rare event, and only a few cases have been reported in the medical literature. The extent of the deletion and the genotype-phenotype correlation are 2 crucial issues.Du

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::fd7fa0b397d03264a9a3e4f89a3fb018
https://pubmed.ncbi.nlm.nih.gov/21447942

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