𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Refined gene localization for MRX7

✍ Scribed by Tackels, Darci; Schwartz, Charles E.; Thibodeau, Steven N.; Michels, Virginia V.


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
16 KB
Volume
85
Category
Article
ISSN
0148-7299
DOI
10.1002/(sici)1096-8628(19990730)85:3<288::aid-ajmg20>3.0.co;2-y

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Refined gene localization for MRX8
✍ Tackels, Darci; Schwartz, Charles E. πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 14 KB πŸ‘ 2 views
Regional localization of a gene for nons
✍ Claes, Stephan; Volcke, Philippe; Devriendt, Koenraad; Holvoet, Maureen; Raeymae πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 71 KB πŸ‘ 1 views

Two families with nonspecific X-linked mental retardation (MRX) are presented. In the first family, MRX51, three male patients showed mild to borderline mental retardation. Multipoint linkage analysis yielded a maximal LOD score of 2.10 between markers DXS8012 and DXS1003, localizing the MRX51 gene

cover
✍ Fresco, Paolo πŸ“‚ Fiction πŸ“… 2020 πŸ› Baldini & Castoldi 🌐 Italian βš– 267 KB

L’irresistibile ascesa di un ragazzo italiano diventato uno dei manager piΓΉ potenti d’America, prima di prendere il timone della Fiat e cambiare per sempre il capitalismo industriale del nostro paese. È la storia di uno studente di Genova – compagno di scuola di Paolo Villaggio e oggetto delle sue p

Refined 2.7 centimorgan locus in Xp21.3-
✍ Jemaa, Lamia Ben; des Portes, Vincent; Zemni, Ramzi; Mrad, Ridha; Maazoul, Faouz πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 75 KB πŸ‘ 1 views

Nonspecific X-linked mental retardation (MRX) is a heterogeneous condition in which mental retardation (MR) appears to be the only consistent manifestation. A large genetic interval of assignment obtained on individual families by linkage analysis, genetic, heterogeneity, and phenotypic variability

Localization of a novel gene for nonsynd
✍ Greinwald, John H.; Wayne, Sigrid; Chen, Achih H.; Scott, Daryl A.; Zbar, Ross I πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 63 KB πŸ‘ 2 views

## Autosomal recessive nonsyndromic hearing loss (ARNSHL) is the most common form of hereditary hearing impairment (HHI). To date, 16 different loci have been reported, making ARNSHL an extremely heterogeneous disorder. One of these loci, DFNB4, was mapped to a 5-cM interval of 7q31 in a large Midd

Synteny-defined candidate genes for cong
✍ Giampietro, Philip F.; Raggio, Cathleen L.; Blank, Robert D. πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 44 KB πŸ‘ 2 views

Idiopathic scoliosis (IS) is a common but poorly understood syndrome. Congenital scoliosis (CS) is less common but comparably unexplored. Previous studies suggest that each has a significant genetic component. However, the occurrence of scoliosis in the presence of other hereditary connective tissue