✦ LIBER ✦

Linkage disequilibrium between aSacI restriction fragment length polymorphism and two galactosemia mutations

✍ Scribed by Hsien-Chin Lin; Juergen K. V. Reichardt

Publisher: Springer
Year: 1995
Tongue: English
Weight: 333 KB
Volume: 95
Category: Article
ISSN: 0340-6717
DOI: 10.1007/bf00225208

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Detection of linkage between restriction

Detection of linkage between restriction fragment length polymorphism markers and quantitative traits

✍ M. J. Asins; E. A. Carbonell 📂 Article 📅 1988 🏛 Springer 🌐 English ⚖ 339 KB

Methodologies commonly used to detect linkage of marker loci to loci affecting quantitative traits are discussed. It is shown that variances for the quantitative trait differ among marker genotypes when using F2 or pooled backcross data if linkage exists. Hence, to analyze this type of data by singl

Correction: Detection of linkage between

Correction: Detection of linkage between quantitative trait loci and restriction fragment length polymorphism using inbred lines

✍ S. P. Simpson 📂 Article 📅 1992 🏛 Springer 🌐 English ⚖ 134 KB

Detection of linkage between quantitativ

Detection of linkage between quantitative trait loci and restriction fragment length polymorphisms using inbred lines

✍ S. P. Simpson 📂 Article 📅 1989 🏛 Springer 🌐 English ⚖ 476 KB

In segregating populations, large numbers of individuals are needed to detect linkage between markers, such as restriction fragment length polymorphisms (RFLPs), and quantitative trait loci (QTL), limiting the potential use of such markers for detecting linkage. Fewer individuals from inbred lines a

Close linkage between X-linked ectoderma

Close linkage between X-linked ectodermal dysplasia and a cloned DNA sequence detecting a two allele restriction fragment length polymorphism in the region Xp11-q12

✍ Steen Kølvraa; Torben A. Kruse; P. K. A. Jensen; Kirsten H. Linde; Søren R. Vest 📂 Article 📅 1986 🏛 Springer 🌐 English ⚖ 382 KB

EDA (ectodermal dysplasia, anhidrotic) is an X-linked recessive disorder characterized by hypohidrosis, hypoor anodontia, and hypotrichosis. A possible linkage between the gene for EDA and a number of restriction fragment length polymorphisms (RFLPs) spread over the X chromosome was investigated in

Linkage between a PvuII restriction frag

Linkage between a PvuII restriction fragment length polymorphism and G6PD A-202A/376G: evidence for a single origin of the common G6PD A — mutation

✍ Ernest Beutler; Wanda Kuhl 📂 Article 📅 1990 🏛 Springer 🌐 English ⚖ 288 KB

DNA samples from 29 males with the G6PD A- phenotype and 14 males with a G6PD B phenotype were studied for the presence of each of four polymorphic restriction sites in the glucose-6-phosphate dehydrogenase locus. All G6PD A- subjects with the G6PD A-202A/376G genotype, regardless of population orig

Associations between restriction fragmen

Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiency

✍ E. Mornet; P. Couillin; F. Kutten; M. C. Raux; P. C. White; D. Cohen; A. Boué; J 📂 Article 📅 1986 🏛 Springer 🌐 English ⚖ 1019 KB