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Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome

Nondisjunction in trisomy 21 has traditionally been studied by cytogenetic heteromorphisms. Those studies assumed no crossing-over on the short arm of chromosome 21. Recently, increased accuracy of detection of the origin of nondisjunction has been demonstrated by DNA polymorphism analysis. We descr...

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Autors principals: Petersen, Michael B., Frantzen, Merete, Antonarakis, Stylianos E., Warren, Andrew C., Van Broeckhoven, Christine, Chakravarti, Aravinda, Cox, Tara K., Lund, Connie, Olsen, Bodil, Poulsen, Hanne, Sand, Annie, Tommerup, Niels, Mikkelsen, Margareta
Format: Artigo
Idioma:Inglês
Publicat: 1992
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682728/
https://ncbi.nlm.nih.gov/pubmed/1386710
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