๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

No evidence for chromosomal microdeletions at the second DiGeorge syndrome locus on 10p near D10S585

โœ Scribed by Bartsch, Oliver; Wagner, Annett; Hinkel, Georg Klaus; Lichtner, Peter; Murken, Jan; Schuffenhauer, Simone


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
13 KB
Volume
83
Category
Article
ISSN
0148-7299
DOI
10.1002/(sici)1096-8628(19990423)83:5<425::aid-ajmg17>3.0.co;2-q

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


DiGeorge anomaly and chromosome 10p dele
โœ Dasouki, Majed; Jurecic, Vesna; Phillips, John A.; Whitlock, James A.; Baldini, ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 18 KB ๐Ÿ‘ 2 views

We report on a patient with DiGeorge syndrome (DGS) phenotype or anomaly and an unbalanced translocation [45,XY,-10,-22, +der(10),t(10;22)(p13;q11)] resulting in monosomy of 10p13-pter and 22q11-pter. Because both regions involved in this rearrangement have been implicated in DGS, we performed a mol

Suggestive evidence of a locus on chromo
โœ Foroud, Tatiana; Castelluccio, Peter F.; Koller, Daniel L.; Edenberg, Howard J.; ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 16 KB

## As part of a four-center NIMH Genetics Initiative on Bipolar Disorder, a genome screen using 365 markers was performed on 540 DNAs from 97 families, enriched for affected relative pairs. This is the largest uniformly ascertained and assessed linkage sample for this disease, and includes 232 subj

Further evidence for a susceptibility lo
โœ Schwab, Sibylle G.; Hallmayer, Joachim; Albus, Margot; Lerer, Bernard; Hanses, C ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 26 KB ๐Ÿ‘ 1 views

## Recent reports on potential linkage by Faraone and the NIMH Genetics Initiative-Millennium Schizophrenia Consortium [1997: Am J Med Genet 74:557], and by Straub et al. [1997: Am J Med Genet 74:558], prompted us to study chromosome 10 in a sample of 72 families containing 2 or more affected sibs

No evidence for a major susceptibility l
โœ Durner, Martina; Shinnar, Shlomo; Resor, Stanley R.; Moshe, Solomon L.; Rosenbau ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 19 KB ๐Ÿ‘ 1 views

Juvenile myoclonic epilepsy (JME) is a distinct epileptic syndrome with a complex mode of inheritance. Several studies found evidence for a locus involved in JME on chromosome 6 near the HLA region. Recently, Elmslie et al. [1997] reported evidence of linkage in JME to chromosome 15q14 assuming a re

Hereditary febrile seizures: Phenotype a
โœ Kugler, Steven L.; Stenroos, E. Scot; Mandelbaum, David E.; Lehner, Thomas; McKo ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 62 KB ๐Ÿ‘ 1 views

The occurrence of febrile seizures (FSs) in large autosomal dominant FS kindreds makes possible accurate delineation of the pure clinical phenotype of hereditary FS among secondary FS cases, and the identification of gene loci causing susceptibility to FS. Recently FS gene loci on chromosomes 8 and

cover
โœ Bethany Lopez ๐Ÿ“‚ Fiction ๐Ÿ“… 2015 ๐Ÿ› Bethany Lopez ๐ŸŒ English โš– 143 KB ๐Ÿ‘ 1 views

A lot can happen in 10 years, and Gwen and Craig have been there for each other through it all, from meeting on the playground to juggling college finals. But their long-standing friendship hasn't been without its challenges. Gwen keeps her emotions locked down tight, and when someone hurts her