Literature DB >> 2877813

A polymorphic human myosin heavy chain locus is linked to an anonymous single copy locus (D17S1) at 17p13.

C E Schwartz, E McNally, L Leinwand, M H Skolnick.   

Abstract

Restriction fragment length polymorphisms (RFLPs) have been developed for an adult human skeletal muscle myosin heavy chain gene which was previously mapped to the short arm of human chromosome 17. Using RFLP analysis of DNA from 140 individuals, we have found tight linkage (LOD score of 6.9) between this myosin heavy chain gene and the anonymous DNA probe, D17S1.

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Year:  1986        PMID： 2877813     DOI： 10.1159/000132307

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN： 0301-0171


  11 in total

1.  Organization of human and mouse skeletal myosin heavy chain gene clusters is highly conserved.

Authors:  A Weiss; D McDonough; B Wertman; L Acakpo-Satchivi; K Montgomery; R Kucherlapati; L Leinwand; K Krauter
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-16       Impact factor: 11.205

2.  Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21.

Authors:  C E Schwartz; J Ulmer; A Brown; I Pancoast; H O Goodman; R E Stevenson
Journal:  Am J Hum Genet       Date:  1990-09       Impact factor: 11.025

3.  PstI RFLP at the MYH2 locus on chromosome 17.

Authors:  C Schwartz
Journal:  Nucleic Acids Res       Date:  1990-05-11       Impact factor: 16.971

4.  Detection of submicroscopic deletions in band 17p13 in patients with the Miller-Dieker syndrome.

Authors:  C E Schwartz; J P Johnson; B Holycross; T M Mandeville; T S Sears; E A Graul; J C Carey; R J Schroer; M C Phelan; J Szollar
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025

5.  Arch fingerprints, hypotonia, and areflexia associated with X linked mental retardation.

Authors:  R E Stevenson; B Häne; J F Arena; M May; L Lawrence; H A Lubs; C E Schwartz
Journal:  J Med Genet       Date:  1997-06       Impact factor: 6.318

6.  The parental origin and mechanism of formation of three dicentric X chromosomes.

Authors:  M C Phelan; L A Prouty; R E Stevenson; P N Howard-Peebles; D C Page; C E Schwartz
Journal:  Hum Genet       Date:  1988-09       Impact factor: 4.132

7.  Mapping of Alport syndrome to the long arm of the X chromosome.

Authors:  C L Atkin; S J Hasstedt; L Menlove; L Cannon; N Kirschner; C Schwartz; K Nguyen; M Skolnick
Journal:  Am J Hum Genet       Date:  1988-02       Impact factor: 11.025

8.  Two sisters with a distal deletion at the Xq26/Xq27 interface: DNA studies indicate that the gene locus for factor IX is present.

Authors:  C Schwartz; N Fitch; M C Phelan; C L Richer; R Stevenson
Journal:  Hum Genet       Date:  1987-05       Impact factor: 4.132

9.  Assignment of the Charcot-Marie-Tooth neuropathy type 1 (CMT 1a) gene to 17p11.2-p12.

Authors:  V Timmerman; P Raeymaekers; P De Jonghe; G De Winter; L Swerts; K Jacobs; J Gheuens; J J Martin; A Vandenberghe; C Van Broeckhoven
Journal:  Am J Hum Genet       Date:  1990-10       Impact factor: 11.025

10.  Deletion (X)(q26.1-->q28) in a proband and her mother: molecular characterization and phenotypic-karyotypic deductions.

Authors:  A T Tharapel; K P Anderson; J L Simpson; P R Martens; R S Wilroy; J C Llerena; C E Schwartz
Journal:  Am J Hum Genet       Date:  1993-03       Impact factor: 11.025
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