Literature DB >> 511167

Prenatal diagnosis of a 13p+ karyotype.

D Soudek.   

Abstract

Chromosome 13p+ was identified in an amniotic cell culture. The variant has been inherited for three generations without adverse effect.

Mesh：

Year:  1979        PMID： 511167     DOI： 10.1007/bf00283406

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  6 in total

1.  A 6p trisomy detected in a family with a "giant satellite".

Authors:  H Chiyo; Y Kuroki; I Matsui; K Yanagida; Y Nakagome
Journal:  Humangenetik       Date:  1975-10-20

2.  Familial 13p+ chromosome with mental retardation and dysmorphic features of two children.

Authors:  C Stoll; A Rohmer; R Korn; G Heumann
Journal:  Hum Genet       Date:  1976-09-10       Impact factor: 4.132

3.  Size variation polymorphisms of the short arm of human acrocentric chrosomes determined by R-banding by fluorescence using acridine orange (RFA).

Authors:  R S Verma; H Dosik; H A Lubs
Journal:  Hum Genet       Date:  1977-09-22       Impact factor: 4.132

4.  Cytogenetic and linkage studies of a familial 15pplus variant.

Authors:  F E Yoder; W B Bias; D S Borgaonkar; G F Bahr; I I Yoder; O C Yoder; H M Golomb
Journal:  Am J Hum Genet       Date:  1974-09       Impact factor: 11.025

5.  Giant satellites or translocation?

Authors:  M G Wilson; A Fujimoto; N W Shinno; J W Towner
Journal:  Cytogenet Cell Genet       Date:  1973

6.  [Karyotype 46,XY,22p+ in a male patient (author's transl)].

Authors:  N Trabalza; M Furbetta; G Rosi; E Donti; G Venti; G Migliorini Bruschelli
Journal:  J Genet Hum       Date:  1978-06
  6 in total

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