Literature DB >> 1981991

A detailed multipoint gene map of chromosome 1q.

K H Buetow1, D Nishimura, Y Nakamura, O Jiang, J C Murray.   

Abstract

Utilizing genotyping data for 23 markers, we have constructed a 21-locus multipoint genetic map of the long arm of chromosome 1. Five new RFLPs are reported. The map integrates anonymous loci from previous primary linkage maps and incorporates markers for 10 coding sequences. These markers form a continuous linkage group of 85 cM in males and 141 cM in females. The map was constructed employing the LINKAGE and CRIMAP computational methodologies via a stepwise algorithm.

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Year:  1990        PMID： 1981991     DOI： 10.1016/0888-7543(90)90220-o

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


  10 in total

1.  Framework multipoint map of the long arm of human chromosome 4 and telomeric localization of the gene for FSHD.

Authors:  B Weiffenbach; R G Bagley; K Falls; J Dubois; C Hyser; D Storvick; P Schultz; J R Mendell; E C Milner; S J Jacobsen
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

Review 2.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M R Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

3.  A dinucleotide repeat for the D1S53 locus.

Authors:  D Y Nishimura; N J Leysens; J C Murray
Journal:  Nucleic Acids Res       Date:  1992-03-11       Impact factor: 16.971

4.  Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD).

Authors:  K A Mills; K H Buetow; Y Xu; T M Ritty; K D Mathews; S E Bodrug; C Wijmenga; I Balazs; J C Murray
Journal:  Am J Hum Genet       Date:  1992-08       Impact factor: 11.025

Review 5.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

6.  Linkage of Van der Woude syndrome (VWS) to REN and exclusion of the candidate gene TGFB2 from the disease locus in a large pedigree.

Authors:  A Sander; H Moser; S Liechti-Gallati; T Grimm; M Zingg; J Raveh
Journal:  Hum Genet       Date:  1993-03       Impact factor: 4.132

7.  Exclusion of candidate genes from a role in cleft lip with or without cleft palate: linkage and association studies.

Authors:  G M Vintiner; K K Lo; S E Holder; R M Winter; S Malcolm
Journal:  J Med Genet       Date:  1993-09       Impact factor: 6.318

8.  Microsatellite-based fine mapping of the Van der Woude syndrome locus to an interval of 4.1 cM between D1S245 and D1S414.

Authors:  A Sander; J C Murray; T Scherpbier-Heddema; K H Buetow; J Weissenbach; M Zingg; K Ludwig; R Schmelzle
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

9.  The gene encoding human transmembrane secretory component (locus PIGR) is linked to D1S58 on chromosome 1.

Authors:  P Krajci; T Gedde-Dahl; B Høyheim; S Rogde; B Olaisen; P Brandtzaeg
Journal:  Hum Genet       Date:  1992-11       Impact factor: 4.132

10.  Evidence for linkage of the apolipoprotein A-II locus to plasma apolipoprotein A-II and free fatty acid levels in mice and humans.

Authors:  C H Warden; A Daluiski; X Bu; D A Purcell-Huynh; C De Meester; B H Shieh; D L Puppione; R M Gray; G M Reaven; Y D Chen
Journal:  Proc Natl Acad Sci U S A       Date:  1993-11-15       Impact factor: 11.205
  10 in total

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