Literature DB >> 2335351

A genetic map of human chromosome 17p.

E C Wright1, D E Goldgar, P R Fain, D F Barker, M H Skolnick.   

Abstract

A genetic linkage map was constructed with 18 loci from the short arm and pericentric region of chromosome 17 typed on the CEPH reference families. The genetic map includes three markers extracted from the CEPH public database. Nine loci could be ordered using a threshold of odds of at least 1000:1 against alternative orders during the map construction process. With a reduced tolerance of 100:1, a total of 13 loci could be placed on the map spanning a distance of approximately 60 cM in females and 46 cM in males. There were statistically significant differences between the male and the female genetic maps. The order inferred from the genetic data was consistent with the physical localizations of these probes obtained from somatic cell hybrids and tumor deletion studies. This map should be useful for genetic fine mapping of 17p loci.

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Year:  1990        PMID: 2335351     DOI: 10.1016/0888-7543(90)90524-x

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


  19 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

2.  Involvement of multiple chromosome 17p loci in medulloblastoma tumorigenesis.

Authors:  P H Cogen; L Daneshvar; A K Metzger; G Duyk; M S Edwards; V C Sheffield
Journal:  Am J Hum Genet       Date:  1992-03       Impact factor: 11.025

3.  Molecular mapping of four ovule lethal mutants in soybean.

Authors:  K K Kato; R G Palmer
Journal:  Theor Appl Genet       Date:  2003-11-11       Impact factor: 5.699

4.  The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications.

Authors:  G Floridia; M Piantanida; A Minelli; C Dellavecchia; C Bonaglia; E Rossi; G Gimelli; G Croci; F Franchi; S Gilgenkrantz; P Grammatico; L Dalprá; S Wood; C Danesino; O Zuffardi
Journal:  Am J Hum Genet       Date:  1996-04       Impact factor: 11.025

5.  The duplication in Charcot-Marie-Tooth disease type 1a spans at least 1100 kb on chromosome 17p11.2.

Authors:  J E Hoogendijk; G W Hensels; I Zorn; L Valentijn; E A Janssen; M de Visser; D F Barker; B W Ongerboer de Visser; F Baas; P A Bolhuis
Journal:  Hum Genet       Date:  1991-12       Impact factor: 4.132

6.  Partitioned pulsed-field gel electrophoresis-PCR (PPF-PCR): a new method for pulsed-field mapping for STS and microsatellites.

Authors:  P H Denton; J B Cullen; D Loeb; A Lucas; K Nunes; C Hulett; J M Vance
Journal:  Nucleic Acids Res       Date:  1994-05-11       Impact factor: 16.971

7.  Charcot-Marie-Tooth disease type 1a (CMT1a): evidence for trisomy of the region p11.2 of chromosome 17 in south Wales families.

Authors:  J C MacMillan; M Upadhyaya; P S Harper
Journal:  J Med Genet       Date:  1992-01       Impact factor: 6.318

8.  Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group.

Authors:  P Raeymaekers; V Timmerman; E Nelis; W Van Hul; P De Jonghe; J J Martin; C Van Broeckhoven
Journal:  J Med Genet       Date:  1992-01       Impact factor: 6.318

9.  Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMTIA duplication.

Authors:  C A Wise; C A Garcia; S N Davis; Z Heju; L Pentao; P I Patel; J R Lupski
Journal:  Am J Hum Genet       Date:  1993-10       Impact factor: 11.025

10.  Duplication within chromosome 17p11.2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type 1a. The French CMT Research Group.

Authors:  A Brice; N Ravisé; G Stevanin; M Gugenheim; P Bouche; C Penet; Y Agid
Journal:  J Med Genet       Date:  1992-11       Impact factor: 6.318

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