Literature DB >> 1973839

Dinucleotide repeat polymorphisms at the DXS453, DXS454 and DXS458 loci.

J L Weber1, A E Kwitek, P E May, M H Polymeropoulos, S Ledbetter.   

Abstract

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Year:  1990        PMID： 1973839      PMCID： PMC331150          DOI： 10.1093/nar/18.13.4037

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  2 in total

1.  Five polymorphic microsatellite VNTRs on the human X chromosome.

Authors:  J A Luty; Z Guo; H F Willard; D H Ledbetter; S Ledbetter; M Litt
Journal:  Am J Hum Genet       Date:  1990-04       Impact factor: 11.025

2.  Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction.

Authors:  J L Weber; P E May
Journal:  Am J Hum Genet       Date:  1989-03       Impact factor: 11.025
  2 in total
  22 in total

1.  Exclusion mapping of the X-linked dominant chondrodysplasia punctata/ichthyosis/cataract/short stature (Happle) syndrome: possible involvement of an unstable pre-mutation.

Authors:  H Traupe; D Müller; D Atherton; D C Kalter; F P Cremers; B A van Oost; H H Ropers
Journal:  Hum Genet       Date:  1992-08       Impact factor: 4.132

2.  Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysis.

Authors:  K A Ellison; C P Fill; J Terwilliger; L J DeGennaro; A Martin-Gallardo; M Anvret; A K Percy; J Ott; H Zoghbi
Journal:  Am J Hum Genet       Date:  1992-02       Impact factor: 11.025

3.  Generation of sequence-tagged sites from Xp22.3 by isolating common Alu-PCR products of radiation hybrids retaining overlapping human X chromosome fragments.

Authors:  I A Glass; M Passage; L Bernatowicz; E C Salido; T Mohandas; P H Yen; L J Shapiro
Journal:  Hum Genet       Date:  1996-05       Impact factor: 4.132

4.  X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26.

Authors:  M Lagerström-Fermér; M Sundvall; E Johnsen; G L Warne; S M Forrest; J D Zajac; A Rickards; D Ravine; U Landegren; U Pettersson
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

5.  Refined genetic mapping of X-linked Charcot-Marie-Tooth neuropathy.

Authors:  P R Fain; D F Barker; P F Chance
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

6.  High-resolution mapping of the X-linked hypohidrotic ectodermal dysplasia (EDA) locus.

Authors:  J Zonana; M Jones; D Browne; M Litt; P Kramer; H W Becker; N Brockdorff; S Rastan; K P Davies; A Clarke
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

7.  Exclusion mapping of the gene for X-linked neural tube defects in an Icelandic family.

Authors:  F A Hol; M P Geurds; O Jensson; B C Hamel; G E Moore; R Newton; E C Mariman
Journal:  Hum Genet       Date:  1994-04       Impact factor: 4.132

8.  Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies.

Authors:  S J Scheinman; M A Pook; C Wooding; J T Pang; P A Frymoyer; R V Thakker
Journal:  J Clin Invest       Date:  1993-06       Impact factor: 14.808

9.  Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragment.

Authors:  J Zonana; J Gault; K J Davies; M Jones; D Browne; M Litt; N Brockdorff; S Rastan; A Clarke; N S Thomas
Journal:  Am J Hum Genet       Date:  1993-01       Impact factor: 11.025

10.  Linkage localization of X-linked Charcot-Marie-Tooth disease.

Authors:  J Bergoffen; J Trofatter; M A Pericak-Vance; J L Haines; P F Chance; K H Fischbeck
Journal:  Am J Hum Genet       Date:  1993-02       Impact factor: 11.025
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