Maternal origin of a de novo balanced t(21q21q) identified by ets-2 polymorphism

Author:

Créau-Goldberg Nicole,Gegonne Anne,Delabar Jean,Cochet Chantal,Cabanis Marie-Odile,Stehelin Dominique,Turleau Catherine,de Grouchy Jean

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Reference9 articles.

1. Feinberg AP, Vogelstein B (1983) A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal Biochem 132:6?13. Addendum (1984) Anal Biochem 137: 266?267

2. Kirkels VGH, Hustinx TWJ, Scheres JMJC (1980) Habitual abortion and translocation (22q;22q): unexpected transmission from a mother to her phenotypically normal daughter. Clin Genet 18: 456?461

3. Martin RH, Balkan W, Burns K, Rademaker AW, Lin CC, Rudd NL (1983) The chromosome constitution of 1000 human spermatozoa. Hum Genet 63:305?309

4. Millington-Ward A, Wassenaar ALM, Pearson PL (1985) Restriction fragment length polymorphic probes in the analysis of Down's syndrome. (8th International Congress on Human Gene Mapping) Cytogenet Cell Genet 40:699

5. Münke M, Kraus J, Watkins P, Tanzi R, Gusella J, Millington-Ward A, Watson M, Francke U (1985) Homocystinuria gene on chromosome 21 mapped with cloned cystathionine beta-synthase probe and in situ hybridization of other chromosome 21 probes. (8th International Congress on Human Gene Mapping) Cytogenet Cell Genet 40:706?707

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