Literature DB >> 5480968

A 46,XX,t(Cp+;Cq-) translocation in a girl with multiple congenital anomalies and in her phenotypically normal father 46,XY,t(Cq+;Cq-).

G J Bargman, R L Neu, H O Powers, L I Gardner.   

Abstract

Entities:  

Mesh：

Year:  1970        PMID： 5480968      PMCID： PMC1468895          DOI： 10.1136/jmg.7.1.77

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  5 in total

1.  TURNER'S SYNDROME WITH SECONDARY AMENORRHOEA AND SEX CHROMOSOME MOSAICISM.

Authors:  D R LONDON; N H KEMP; J R ELLIS; U MITTWOCH
Journal:  Acta Endocrinol (Copenh)       Date:  1964-07

2.  MATERNAL TRANSMISSION OF A NEW GROUP-C(6/9) CHROMOSOMAL SYNDROME.

Authors:  R A ROHDE; B CATZ
Journal:  Lancet       Date:  1964-10-17       Impact factor: 79.321

3.  A FAMILIAL 4/5 RECIPROCAL TRANSLOCATION RESULTING IN PARTIAL TRISOMY B.

Authors:  M W SHAW; M M COHEN; H M HILDERBRANDT
Journal:  Am J Hum Genet       Date:  1965-01       Impact factor: 11.025

4.  MEIOTIC AND MITOTIC STUDIES OF A FAMILIAL RECIPROCAL TRANSLOCATION BETWEEN TWO AUTOSOMES OF GROUP 6-12.

Authors:  J LINDSTEN; M FRACCARO; H P KLINGER; P ZETTERQVIST
Journal:  Cytogenetics       Date:  1965

5.  [Partial trisomy C through a familial translocation t(Cq+;Cq-)].

Authors:  J Lejeune; M O Rethoré; R Berger; D Abonyi; B Dutrillaux; G See
Journal:  Ann Genet       Date:  1968-09
  5 in total
  1 in total

1.  Trisomy 12p due to familial t(12p-,6q plus) translocation.

Authors:  J P Fryns; H Van Den Berghe
Journal:  Humangenetik       Date:  1974
  1 in total

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