Literature DB >> 28052341

EDA mutation by exome sequencing in non-syndromic X-linked oligodontia.

L Martins1, R A Machado2, D S Araujo3, P A Giovani3, P D Rebouças3, L P Rodrigues3, L S Mofatto4, M M Ribeiro5, L L Coutinho6, R M Puppin-Rontani3, R D Coletta2, F H Nociti1, K R Kantovitz3,7.   

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Year:  2017        PMID: 28052341     DOI: 10.1111/cge.12961

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


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  1 in total

1.  Genetic diagnosis for X-linked hypohidrotic ectodermal dysplasia family with a novel Ectodysplasin A gene mutation.

Authors:  Xin Ma; Xue Lv; Hong-Yan Liu; Xing Wu; Li Wang; Hao Li; Hai-Yan Chou
Journal:  J Clin Lab Anal       Date:  2018-07-13       Impact factor: 2.352

  1 in total

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