Literature DB >> 4394837

[Multiple congenital malformations in a boy with a chromosome abnormality of the group F (46-XY, 20-P), the son of a clinically healthy subject with an analogous chromosome malformation].

G Loiodice, D G Rovetta, G Bellicini, G Callura, F Bergamo.   

Abstract

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Year:  1970        PMID： 4394837

Source DB:  PubMed          Journal:  Minerva Pediatr        ISSN： 0026-4946            Impact factor:   1.312


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  5 in total

1.  Deletion of the short arms of chromosome 20.

Authors:  D K Kalousek; S Thérien
Journal:  Hum Genet       Date:  1976-09-10       Impact factor: 4.132

2.  Ring F chromosome mosaicism (46,XY,20r-46,XY) in an epileptic child without apparent haematological disease.

Authors:  M Faed; H G Morton; J Robertson
Journal:  J Med Genet       Date:  1972-12       Impact factor: 6.318

3.  Segregation analysis of Alagille syndrome.

Authors:  S Dhorne-Pollet; J F Deleuze; M Hadchouel; C Bonaïti-Pellié
Journal:  J Med Genet       Date:  1994-06       Impact factor: 6.318

4.  Deleted chromosome 20 from a patient with Alagille syndrome isolated in a cell hybrid through leucine transport selection: study of three candidate genes.

Authors:  J F Deleuze; S Dhorne; J Hazan; E Borghi; N Raynaud; N Pollet; M Meunier-Rotival; J Deschatrette; D Alagille; M Hadchouel
Journal:  Mamm Genome       Date:  1994-11       Impact factor: 2.957

5.  Molecular and cytogenetic analysis of an interstitial 20p deletion associated with syndromic intrahepatic ductular hypoplasia (Alagille syndrome).

Authors:  S Schnittger; C Höfers; P Heidemann; F Beermann; I Hansmann
Journal:  Hum Genet       Date:  1989-10       Impact factor: 4.132
  5 in total

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