Literature DB >> 4242066

Familial translocation (3?--;G?- q+) and nondisjunction of chromosome in group G in two unrelated families.

S W Soukup, E Passarge, D M Becroft, R L Shaw, L G Young.   

Abstract

Mesh:

Year:  1969        PMID: 4242066

Source DB:  PubMed          Journal:  Cytogenetics        ISSN: 0011-4537


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  7 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.  Familial translocation t(3p-;21q+) associated with both Down's and Sturge-Weber's syndrome in unbalanced state.

Authors:  M Habedank; G Kampe
Journal:  Humangenetik       Date:  1975-09-23

3.  Reciprocal translocation, 4q-; 21p+, giving rise to Down's syndrome.

Authors:  M B Jenkins; L Boyd
Journal:  J Med Genet       Date:  1976-08       Impact factor: 6.318

4.  An unusual chromosomal segregation in a family with a translocation between chromosomes 3 and 12.

Authors:  S Sachdeva; G F Smith; P Justice
Journal:  J Med Genet       Date:  1974-09       Impact factor: 6.318

5.  A rare translocation (47,XY,t(2p-;21q+),21+) associated with Down's syndrome.

Authors:  J R Miller; F J Dill; M J Corey; J M Rigg
Journal:  J Med Genet       Date:  1970-12       Impact factor: 6.318

Review 6.  Down's syndrome. Current stage of cytogenetic research.

Authors:  M Mikkelsen
Journal:  Humangenetik       Date:  1971

7.  Multiple congenital defects associated with trisomy for long arm of No. 4.

Authors:  M Issa; A M Potter; C E Blank
Journal:  J Med Genet       Date:  1976-08       Impact factor: 6.318

  7 in total

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