The meiotic stage of nondisjunction in trisomy 21: Determination by using DNA polymorphisms

We have studied DNA polymorphisms at loci in the pericentromeric region on the long arm of chromosome 21 in 200 families with trisomy 21, in order to determine the meiotic origin of nondisjunction. Maintenance of heterozygosity for parental markers in the individual with trisomy 21 was interpreted a...

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Main Authors: Antonarakis, Stylianos E., Petersen, Michael B., McInnis, Melvin G., Adelsberger, Patricia A., Schinzel, Albert A., Binkert, Franz, Pangalos, Constantine, Raoul, Odile, Slaugenhaupt, Susan A., Hafez, Mohamed, Cohen, Maimon M., Roulson, Diane, Schwartz, Stuart, Mikkelsen, Margareta, Tranebjaerg, Lisbeth, Greenberg, Frank, Hoar, David I., Rudd, Noreen L., Warren, Andrew C., Metaxotou, Caterina, Bartsocas, Christos, Chakravarti, Aravinda
Formato: Artigo
Idioma:Inglês
Publicado em: 1992
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1684265/
https://ncbi.nlm.nih.gov/pubmed/1347192
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