Literature DB >> 4537722

[Mosaic trisomy 13 with isochromosome: 46, XX-46, XX, 13-, 13 q:].

J M Emberger, C Nègre, R Lafon.   

Abstract

Mesh：

Year:  1972        PMID： 4537722

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


× No keyword cloud information.
  5 in total

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

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

2.  A somatic origin of homologous Robertsonian translocations and isochromosomes.

Authors:  W P Robinson; F Bernasconi; S Basaran; M Yüksel-Apak; G Neri; F Serville; P Balicek; R Haluza; L M Farah; G Lüleci
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

3.  Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX, - 13, + t(13;13)(p11;q11)/46,XX,del(13)(p11).

Authors:  J P Fryns; P Casaer; H Van den Berghe
Journal:  Hum Genet       Date:  1979-01-25       Impact factor: 4.132

4.  Inheritance of a t(13;14)(q10;q10) Robertsonian translocation with a low level of trisomy 13 mosaicism.

Authors:  Jutta Jenderny; Winfried Schmidt; Oliver Bartsch
Journal:  Eur J Pediatr       Date:  2009-12-03       Impact factor: 3.183

5.  Trisomy 22 in a newborn with multiple malformations.

Authors:  I Voiculescu; E Back; A M Duncan; H Schwaibold; W Schempp
Journal:  Hum Genet       Date:  1987-07       Impact factor: 4.132
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.