Literature DB >> 5585048

[Multiple malformations in partial trisomy C (12) as manifestation of an inherited E-C (18/12) translocation].

U K Bühler, E M Bühler, J Sartorius, G R Stalder.   

Abstract

Entities:  

Mesh：

Year:  1967        PMID： 5585048

Source DB:  PubMed          Journal:  Helv Paediatr Acta        ISSN： 0018-022X


× No keyword cloud information.
  6 in total

1.  Trisomy of the short arm of chromosome 10.

Authors:  Y Nakagome; H Kobayashi
Journal:  J Med Genet       Date:  1975-12       Impact factor: 6.318

2.  Prenatal diagnosis of an inherited translocation between chromosomes No. 9 and 18.

Authors:  A J Ebbin; M G Wilson; J W Towner; J P Slaughter
Journal:  J Med Genet       Date:  1973-03       Impact factor: 6.318

3.  [De novo translocation of C-E in clinically atypical E-trisomy syndrome-mosaic: 46,X XX-46, XX, E+, C-t (Cq-; Ep+)].

Authors:  J Hansen
Journal:  Klin Wochenschr       Date:  1970-10-01

4.  On the localization of genes on certain autosomes of man through chromosome aberrations. 3. Exclusion of the possibility of gene assignment.

Authors:  K Bender; K Burckhardt
Journal:  Humangenetik       Date:  1970

5.  [Partial trisomy 10 due to hereditary translocation t(1;10)(q44;q22)].

Authors:  C Laurent; M Bovier-Lapierre; B Dutrillaux
Journal:  Humangenetik       Date:  1973

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

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

北京卡尤迪生物科技股份有限公司 © 2022-2023.