Literature DB >> 5706372

An inherited chromosome aberration in a girl with signs of de Lange syndrome.

K A Broholm, O Eeg-Olofsson, B Hall.   

Abstract

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Year:  1968        PMID： 5706372     DOI： 10.1111/j.1651-2227.1968.tb06978.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN： 0001-656X


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  7 in total

1.  A new case of trisomy for the distal part of 13q due to maternal translocation, t(9;13)(p21;q21).

Authors:  M Jotterand; E Juillard
Journal:  Hum Genet       Date:  1976-08-30       Impact factor: 4.132

2.  Different forms of incomplete trisomy 13. Mosaicism and partial trisomy for the proxim.

Authors:  A Schinzel; W Schmid
Journal:  Humangenetik       Date:  1974

3.  Cornelia de lange syndrome. Report of a case.

Authors:  I C Verma
Journal:  Indian J Pediatr       Date:  1970-04       Impact factor: 1.967

4.  The phenotype in partial 13q trisomies, apropos of a familial (13;15)(q22;q26) translocation.

Authors:  F Rivas; H Rivera; M L Plascencia; B Ibarra; J M Cantú
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

5.  Cornelia de Lange syndrome in several members of the same family.

Authors:  D Kumar; C E Blank; B L Griffiths
Journal:  J Med Genet       Date:  1985-08       Impact factor: 6.318

6.  Chromosome banding study of the Cornelia De Lange syndrome.

Authors:  J R Merikangas; K Merikangas; L Katz; S Pan
Journal:  Hum Genet       Date:  1977-11-10       Impact factor: 4.132

7.  Chromosomes in the Cornelia de Lange syndrome.

Authors:  B Beck; M Mikkelsen
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132
  7 in total

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