๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

The use of DNA markers for carrier detection and prenatal diagnosis of haemophilia A in Egyptian families

โœ Scribed by I. R. HUSSEIN; A. EL-BESHLAWY; A. SALEM; R. MOSAAD; N. ZAGHLOUL; L. RAGAB; H. FAYEK; K. GABER; M. EL-EKIABI


Book ID
108773087
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
122 KB
Volume
14
Category
Article
ISSN
1351-8216

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Prenatal diagnosis and carrier detection
โœ Adel Shalata; Hanna Mandel; Claude Dorche; Marie-Therese Zabot; Stavit Shalev; Y ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 124 KB ๐Ÿ‘ 1 views

Molybdenum cofactor deficiency (MoCoD) is an autosomal recessive, fatal neurological disorder, characterized by the combined deficiency of sulphite oxidase, xanthine dehydrogenase and aldehyde oxidase. We have recently reported an excessive occurrence of this fatal disorder among segments of the Ara

Physical mapping identifies DXS265 as a
โœ Ruth Levering; Angela K. Sweatman; Marie-Anne J. O'Reilly; Sally A. Genet; Helen ๐Ÿ“‚ Article ๐Ÿ“… 1993 ๐Ÿ› Springer ๐ŸŒ English โš– 284 KB

The gene responsible for X-linked agammaglobulinemia (XLA) has not been identified; however, in the course of genetic linkage studies designed to map the locus more precisely, a number of closely linked polymorphic loci have been identified. These have proved to be useful in identifying carriers and