Literature DB >> 939916

Incontinentia pigmenti: a chromosomal breakage syndrome.

T E Kelly, J M Rary, L Young.   

Abstract

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Year:  1976        PMID： 939916     DOI： 10.1093/oxfordjournals.jhered.a108697

Source DB:  PubMed          Journal:  J Hered        ISSN： 0022-1503            Impact factor:   2.645


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  3 in total

1.  Selection against lethal alleles in females heterozygous for incontinentia pigmenti.

Authors:  B R Migeon; J Axelman; S Jan de Beur; D Valle; G A Mitchell; K N Rosenbaum
Journal:  Am J Hum Genet       Date:  1989-01       Impact factor: 11.025

2.  Studies of a family with incontinentia pigmenti variably expressed in both sexes.

Authors:  T W Kurczynski; J S Berns; W E Johnson
Journal:  J Med Genet       Date:  1982-12       Impact factor: 6.318

3.  X-linked dominant inherited diseases with lethality in hemizygous males.

Authors:  R Wettke-Schäfer; G Kantner
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132
  3 in total

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