Detection of mosaicism in lymphocytes of parents of free trisomy 21 offspring

Author:

Frias Sara,Ramos Sandra,Molina Bertha,del Castillo Victoria,Mayén Dora Gilda

Publisher

Elsevier BV

Subject

Health, Toxicology and Mutagenesis,Genetics

Reference62 articles.

1. F. Salamanca (Ed.), Citogenética Humana, 1a Edición, Editorial Médica Panamericana, Mexico, 1990, pp. 117–128.

2. Origin of extra chromosome 21 in 343 families: cytogenetic and molecular approaches;Dagna;Am. J. Med. Suppl.,1990

3. DS: characterization of a case with partial trisomy of chromosome 21 owing to a paternal balanced translocation (15;21)(q26;q22.1) by FISH;Nadal;J. Med. Genet.,1997

4. Parental origin and meiotic stage of non-disjunction in 139 cases of trisomy 21;Ballesta;Ann. Genet.,1999

5. R. McKinlay, G. Sutherland (Eds.), Chromosome abnormalities and Genetic counseling, DS: Other Full Aneuploidies, and Polyploidy, Oxford University Press, New York, 1996, pp. 244–335.

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1. Detección de un mosaico de trisomía 21 en líquido amniótico;Nova;2020-02-10

2. Presence of 15p Marker D15Z1 on the Short Arm of Acrocentric Chromosomes is Associated with Aneuploid Offspring in Mexican Couples;International Journal of Molecular Sciences;2019-10-23

3. Cytogenetic variations in a series of cases of Down Syndrome;Journal of the Anatomical Society of India;2015-06

4. Mosaicism for trisomy 21: A review;American Journal of Medical Genetics Part A;2014-11-20

5. Maternal Germinal Trisomy 21 in Down Syndrome;Journal of Clinical Medicine;2014-01-28

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