Literature DB >> 3478299

A primary genetic linkage map for human chromosome 12.

P O'Connell1, G M Lathrop, M Law, M Leppert, Y Nakamura, M Hoff, E Kumlin, W Thomas, T Elsner, L Ballard.   

Abstract

A primary genetic map for human chromosome 12 has been constructed from data on 23 restriction fragment length polymorphic systems collected in 38 normal families with large sibships. Linkage analysis of the genotypic data has ordered 16 loci into a continuous genetic map of 111 cM in males and 258 cM in females. Although most of the genetic map reflects a higher rate of recombination in females relative to males, significantly more frequent recombination was observed in males than in females in intervals between loci on the distal portion of the short arm of the chromosome. The mapping data shown here will serve as a first step toward a high-resolution genetic map for human chromosome 12.

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Year:  1987        PMID: 3478299     DOI: 10.1016/0888-7543(87)90110-8

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  28 in total

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3.  D12S17 and D12S25 identify the same MspI RFLP.

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4.  Mapping of epidermolysis bullosa simplex mutation to chromosome 12.

Authors:  M Ryynänen; R G Knowlton; J Uitto
Journal:  Am J Hum Genet       Date:  1991-11       Impact factor: 11.025

5.  Polymorphism and mapping of the IGF1 gene, and absence of association with stature among African Pygmies.

Authors:  A Bowcock; V Sartorelli
Journal:  Hum Genet       Date:  1990-08       Impact factor: 4.132

6.  Genetic linkage map of 46 DNA markers on human chromosome 16.

Authors:  T P Keith; P Green; S T Reeders; V A Brown; P Phipps; A Bricker; K Falls; K S Rediker; J A Powers; C Hogan
Journal:  Proc Natl Acad Sci U S A       Date:  1990-08       Impact factor: 11.205

7.  1989 Allen Award address: the American Society of Human Genetics annual meeting, Baltimore.

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8.  Genetic linkage analysis of hereditary arthro-ophthalmopathy (Stickler syndrome) and the type II procollagen gene.

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Journal:  Am J Hum Genet       Date:  1989-11       Impact factor: 11.025

9.  Allelic deletions in the long arm of chromosome 12 identify sites of candidate tumor suppressor genes in male germ cell tumors.

Authors:  V V Murty; J Houldsworth; S Baldwin; V Reuter; W Hunziker; P Besmer; G Bosl; R S Chaganti
Journal:  Proc Natl Acad Sci U S A       Date:  1992-11-15       Impact factor: 11.205

10.  A third gene locus for tuberous sclerosis is closely linked to the phenylalanine hydroxylase gene locus.

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Journal:  Hum Genet       Date:  1991-11       Impact factor: 4.132

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