Literature DB >> 147235

Familial translocation t(lp--;21q+) associated with Down's syndrome.

E Kubień, A Kleczkowska.   

Abstract

Familial occurrence of 1/21 translocation in connection with trisomy 21 was described. The possibilities of inheritance of further chromosome rearrangements arising during the gametogenesis of persons with this translocation were considered.

Entities:  

Mesh：

Year:  1978        PMID： 147235     DOI： 10.1007/bf00272195

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


  5 in total

1.  Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring.

Authors:  R H Lindenbaum; M Bobrow
Journal:  J Med Genet       Date:  1975-03       Impact factor: 6.318

2.  Maternal transmission of a 21/1 translocation associated with Down's syndrome.

Authors:  S B Kontras; G J Currier; R F Cooper; J P Ambuel
Journal:  J Pediatr       Date:  1966-10       Impact factor: 4.406

3.  Banding pattern of human chromosomes.

Authors:  W Schnedl
Journal:  Nat New Biol       Date:  1971-09-15

4.  Rare translocation 47,XY,t(12;21) in Down's syndrome.

Authors:  M Mikkelsen
Journal:  Hum Hered       Date:  1974       Impact factor: 0.444

5.  Identification of a familial 19-21 translocation by Q and G band patterns.

Authors:  W Vogel; B Löning
Journal:  Humangenetik       Date:  1973-05-25
  5 in total

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