A new polymorphic probe on chromosome 6q: p327A (D6S93)
نویسندگان
چکیده
منابع مشابه
A new polymorphic probe on chromosome 22: NB84 (D22S183).
Source/Description: NB84 is a 1.0 kb Hindm-EcoRI fragment isolated from two pooled chromosome 22 specific libraries (AT-CC # 57733 and ATCC # 57714) and is subcloned into pUC9. Polymorphism: PstI digestion of genomic DNA and hybridization with the probe detects a two allele polymorphism: 4.6 kb (Al) and 4.0 kb (A2). No constant bands were present. Chromosomal Localization: Regional localization...
متن کاملA new polymorphic probe on chromosome 22: NB17 (D22S181).
Source/Description: NB17 is a 0.7 kb HindlO-EcoRI fragment isolated from two pooled chromosome 22 specific libraries (AT-CC # 57733 and ATCC # 57714) and was subcloned into pUC9. Polymorphism: Bgin or TaqI digestion of genomic DNA and hybridization with the probe detects a two allele polymorphism: Bgin (Al: 12.5 kb, A2: 4.0 kb) with a constant band at 3.0 kb; TaqI (Bl: 2.9 kb, B2: 2.2 kb). The ...
متن کاملFollow-up study on a susceptibility locus for schizophrenia on chromosome 6q.
Evidence for suggestive linkage to schizophrenia with chromosome 6q markers was previously reported from a two-stage approach. Using nonparametric affected sib pairs (ASP) methods, nominal p-values of 0.00018 and 0.00095 were obtained in the screening (81 ASPs; 63 independent) and the replication (109 ASPs; 87 independent) data sets, respectively. Here, we report a follow-up study of this 50cM ...
متن کاملLung Cancer Risk among Light and Never Smokers A Susceptibility Locus on Chromosome 6q Greatly Increases
Authors' A M.D. Ander Cincinnat Minnesota Detroit, M 6University 7National C Universi ty 9Washingto Institute, G Ohio; and Maryland Note: Supp Research O Correspon ogy, Unive Street, Uni 792-0807;
متن کاملSuggestive linkage to chromosome 6q in families with bilateral vestibulopathy.
BACKGROUND Of the more than 40 genetically defined dominantly inherited hearing loss syndromes, only a few are associated with bilateral vestibulopathy. No genetic mutations have been identified in families with bilateral vestibulopathy and normal hearing. OBJECTIVE To perform a genome-wide scan for linkage in four families with dominantly inherited bilateral vestibulopathy. METHODS Patient...
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ژورنال
عنوان ژورنال: Nucleic Acids Research
سال: 1991
ISSN: 0305-1048,1362-4962
DOI: 10.1093/nar/19.20.5799-a