Literature DB >> 4211154

Analysis for possible linkage between the loci for the Waardenburg syndrome and various blood groups and serological traits.

J L Simpson, C T Falk, G Morillo-Cucci, F H Allen, J German.   

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Year:  1974        PMID： 4211154     DOI： 10.1007/bf00295681

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


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  5 in total

1.  Waardenburg's syndrome.

Authors:  H AASVED
Journal:  Acta Ophthalmol (Copenh)       Date:  1962

2.  Sequential tests for the detection of linkage.

Authors:  N E MORTON
Journal:  Am J Hum Genet       Date:  1955-09       Impact factor: 11.025

3.  A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness.

Authors:  P J WAARDENBURG
Journal:  Am J Hum Genet       Date:  1951-09       Impact factor: 11.025

4.  The Waardenburg syndrome.

Authors:  O A Pantke; M M Cohen
Journal:  Birth Defects Orig Artic Ser       Date:  1971-06

5.  Genetic heterogeneity in the Waardenburg syndrome.

Authors:  S Arias
Journal:  Birth Defects Orig Artic Ser       Date:  1971-03
  5 in total
  3 in total

1.  Probable loose linkage between the ABO locus and Waardenburg syndrome type I.

Authors:  S Arias; M Mota; A Yánez; M Bolivar
Journal:  Humangenetik       Date:  1975

2.  Mouse and hamster mutants as models for Waardenburg syndromes in humans.

Authors:  J H Asher; T B Friedman
Journal:  J Med Genet       Date:  1990-10       Impact factor: 6.318

3.  Assignment of the AK1:Np:ABO linkage group to human chromosome 9.

Authors:  A Westerveld; A P Jongsma; P Meera Khan; H van Someren; D Bootsma
Journal:  Proc Natl Acad Sci U S A       Date:  1976-03       Impact factor: 11.205
  3 in total

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