Literature DB >> 2931983

Recurrence risk in de novo 21q21q translocation Down syndrome.

B D Hall.   

Abstract

Mesh：

Year:  1985        PMID： 2931983     DOI： 10.1002/ajmg.1320220228

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  6 in total

1.  Parental mosaicism in de novo translocation (21q21q) Down's syndrome.

Authors:  G Croci; F Franchi
Journal:  J Med Genet       Date:  1991-07       Impact factor: 6.318

2.  Approaches to the prenatal diagnosis of the Prader-Willi syndrome.

Authors:  A Schinzel
Journal:  Hum Genet       Date:  1986-11       Impact factor: 4.132

3.  Cytogenetic, FISH and DNA studies in 11 individuals from a family with two siblings with dup(21q) Down syndrome.

Authors:  O Bartsch; U König; M B Petersen; H Poulsen; M Mikkelsen; F Palau; F Prieto; E Schwinger
Journal:  Hum Genet       Date:  1993-09       Impact factor: 4.132

4.  Somatic origin of inherited haemophilia A.

Authors:  A H Bröcker-Vriends; E Briët; J C Dreesen; B Bakker; P Reitsma; H Pannekoek; J J van de Kamp; P L Pearson
Journal:  Hum Genet       Date:  1990-08       Impact factor: 4.132

5.  Two progenitor cells for human oogonia inferred from pedigree data and the X-inactivation imprinting model of the fragile-X syndrome.

Authors:  C D Laird; M M Lamb; J L Thorne
Journal:  Am J Hum Genet       Date:  1990-04       Impact factor: 11.025

6.  Are de novo rea(21;21) chromosomes really de novo?

Authors:  Bérénice Hervé; Thibaud Quibel; Stéphane Taieb; Mireille Ruiz; Denise Molina-Gomes; François Vialard
Journal:  Clin Case Rep       Date:  2015-08-26
  6 in total

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