Literature DB >> 5123541

[Complete deletion of the short arm of chromosome 18 and G-18 translocation with dyschromy and hypothyroidism].

G Malpuech, E J Raynaud, J Gaulme, P Godeneche.   

Abstract

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Year:  1971        PMID： 5123541

Source DB:  PubMed          Journal:  Arch Fr Pediatr        ISSN： 0003-9764


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  3 in total

1.  A 46,XY, del(18)(pter leads to p1 100:) cebocephalic child from a 46,XX,t(12;18)(18pter leads to 18 p 1100:: 12qter leads to 12pter) normal parent.

Authors:  G Johnson; R Bachman
Journal:  Hum Genet       Date:  1976-09-10       Impact factor: 4.132

Review 2.  [Ring chromosome 18. 18p-/18q- -deletion-syndrome].

Authors:  J Kunze; E Stephan; M Tolksdorf
Journal:  Humangenetik       Date:  1972

3.  Identification of a 18-21 translocation with Klinefelter's syndrome by G-band patterns.

Authors:  C Waldenmaier; W Hirsch; E König; K Shibata
Journal:  Humangenetik       Date:  1974-03-28
  3 in total

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