Literature DB >> 4177234

Absence of fingerprints in four generations.

H W Baird.   

Abstract

Mesh：

Year:  1968        PMID： 4177234     DOI： 10.1016/s0140-6736(68)91745-5

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  4 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.  [Dysplasia of epidermal ridges with autosomal dominant transmission. Dermatoglyphic studies of one family].

Authors:  P Dodinval; P Leblanc; C Delree; P Deslypere
Journal:  Humangenetik       Date:  1971

4.  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 in total

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