A molecular method for detecting the presence of the human Y chromosome
β Scribed by Friesen, Helena ;Nishioka, Yutaka ;Opitz, John M.
- Book ID
- 118281332
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 398 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0148-7299
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## Abstract Uniparental disomy (UPD) describes the inheritance of both homologues of a pair of chromosomes from only one parent. During the last two decades, the clinical impact of UPD and associated imprinting disorders, such as PraderβWilli syndrome (PWS) and Angelman syndrome (AS) increasingly h
## Abstract Uniparental disomy (UPD) describes the inheritance of both homologues of a pair of chromosomes from only one parent. This condition is often caused by nondisjunction events during meiosis. UPD has been reported as a rare cause of the autosomal recessive disorder and aberrant expression
The Y chromosome is paternally inherited and therefore serves as an evolutionary marker of patrilineal descent. Worldwide DNA variation within the non-recombining portion of the Y chromosome can be represented as a monophyletic phylogenetic tree in which the branches (haplogroups) are defined by at