Literature DB >> 5846547

[Ectodermal dysplasia. Missing papillary pattern, nail disorders and furrows on 4 fingers].

M Basan.   

Abstract

Entities:  

Mesh：

Year:  1965        PMID： 5846547

Source DB:  PubMed          Journal:  Arch Klin Exp Dermatol        ISSN： 0300-8614


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  3 in total

1.  Genetics of patternless finger dermatoglyph.

Authors:  Y FURUYA
Journal:  Jinrui Idengaku Zasshi       Date:  1961-10

2.  [Ectodermal dysplasia of the anhidrotic type; 5 new cases].

Authors:  F PERABO; J A VELASCO; A PRADER
Journal:  Helv Paediatr Acta       Date:  1956-12

3.  [Ectodermal dysplasias and related hereditary syndromes].

Authors:  A FRANCESCHETTI
Journal:  Dermatologica       Date:  1953
  3 in total
  5 in total

1.  Dental defects associated with neonatal symptomatic hypocalcaemia.

Authors:  L Stimmler; G J Snodgrass; E Jaffe
Journal:  Arch Dis Child       Date:  1973-03       Impact factor: 3.791

2.  Congenital malformations of human dermatoglyphs.

Authors:  T J David
Journal:  Arch Dis Child       Date:  1973-03       Impact factor: 3.791

3.  A mutation in a skin-specific isoform of SMARCAD1 causes autosomal-dominant adermatoglyphia.

Authors:  Janna Nousbeck; Bettina Burger; Dana Fuchs-Telem; Mor Pavlovsky; Shlomit Fenig; Ofer Sarig; Peter Itin; Eli Sprecher
Journal:  Am J Hum Genet       Date:  2011-08-04       Impact factor: 11.025

4.  Genome-wide linkage analysis and whole-genome sequencing identify a recurrent SMARCAD1 variant in a unique Chinese family with Basan syndrome.

Authors:  Ming Li; Jianbo Wang; Zhenlu Li; Jia Zhang; Cheng Ni; Ruhong Cheng; Zhirong Yao
Journal:  Eur J Hum Genet       Date:  2016-03-02       Impact factor: 4.246

5.  Two SMARCAD1 Variants Causing Basan Syndrome in a Canadian and a Dutch Family.

Authors:  Youssef Elhaji; Tessa M A van Henten; Claudia A L Ruivenkamp; Mathew Nightingale; Gijs We Santen; Lydia E Vos; Peter R Hull
Journal:  JID Innov       Date:  2021-05-06
  5 in total

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