Literature DB >> 1561107

Dinucleotide repeat polymorphism at the DXS441 locus.

K T Ram1, D F Barker, J M Puck.   

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Year:  1992        PMID： 1561107      PMCID： PMC312202          DOI： 10.1093/nar/20.6.1428

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


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  2 in total

Review 1.  Report of the committee on the genetic constitution of the X chromosome.

Authors:  K E Davies; J L Mandel; A P Monaco; R L Nussbaum; H F Willard
Journal:  Cytogenet Cell Genet       Date:  1990

2.  Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome.

Authors:  R G Lafrenière; C J Brown; V E Powers; L Carrel; K E Davies; D F Barker; H F Willard
Journal:  Genomics       Date:  1991-10       Impact factor: 5.736
  2 in total
  12 in total

1.  New nucleotide sequence data on the EMBL File Server.

Authors: 
Journal:  Nucleic Acids Res       Date:  1992-06-11       Impact factor: 16.971

2.  Molecular analysis of recombination in a family with Duchenne muscular dystrophy and a large pericentric X chromosome inversion.

Authors:  V Shashi; W L Golden; P S Allinson; S H Blanton; C von Kap-Herr; T E Kelly
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

3.  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

4.  The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21).

Authors:  P Saugier-Veber; V Abadie; A Moncla; M Mathieu; C Piussan; C Turleau; J F Mattei; A Munnich; S Lyonnet
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

5.  Trisomy X in a female member of a family with X linked severe combined immunodeficiency: implications for carrier diagnosis.

Authors:  T Lester; M de Alwis; P A Clark; A M Jones; F Katz; R J Levinsky; C Kinnon
Journal:  J Med Genet       Date:  1994-09       Impact factor: 6.318

6.  Refinement of linkage of human severe combined immunodeficiency (SCIDX1) to polymorphic markers in Xq13.

Authors:  J M Puck; M E Conley; L C Bailey
Journal:  Am J Hum Genet       Date:  1993-07       Impact factor: 11.025

7.  Deletion mapping of the DXS986, DXS995, and DXS1002 loci defines their order within Xq21.

Authors:  P A Clark; T Lester; L Villard; M Fontes; C Kinnon
Journal:  J Med Genet       Date:  1994-04       Impact factor: 6.318

8.  Detection of de novo mutations and analysis of their origin in families with X linked hypohidrotic ectodermal dysplasia.

Authors:  J Zonana; M Jones; A Clarke; J Gault; B Muller; N S Thomas
Journal:  J Med Genet       Date:  1994-04       Impact factor: 6.318

9.  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

10.  Two mutational hotspots in the interleukin-2 receptor gamma chain gene causing human X-linked severe combined immunodeficiency.

Authors:  A E Pepper; R H Buckley; T N Small; J M Puck
Journal:  Am J Hum Genet       Date:  1995-09       Impact factor: 11.025
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