Literature DB >> 3472716

Genetic mapping of the human X chromosome: linkage analysis of the q26-q28 region that includes the fragile X locus and isolation of expressed sequences.

J L Mandel, B Arveiler, G Camerino, A Hanauer, R Heilig, M Koenig, I Oberlé.   

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Year:  1986        PMID： 3472716     DOI： 10.1101/sqb.1986.051.01.024

Source DB:  PubMed          Journal:  Cold Spring Harb Symp Quant Biol        ISSN： 0091-7451


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  13 in total

1.  A 230kb cosmid walk in the Duchenne muscular dystrophy gene: detection of a conserved sequence and of a possible deletion prone region.

Authors:  R Heilig; C Lemaire; J L Mandel
Journal:  Nucleic Acids Res       Date:  1987-11-25       Impact factor: 16.971

2.  Rapid PCR analysis of the St14 (DXS52) VNTR.

Authors:  B Richards; R Heilig; I Oberlé; L Storjohann; G T Horn
Journal:  Nucleic Acids Res       Date:  1991-04-25       Impact factor: 16.971

Review 3.  Potential genetic functions of tandem repeated DNA sequence blocks in the human genome are based on a highly conserved "chromatin folding code".

Authors:  P Vogt
Journal:  Hum Genet       Date:  1990-03       Impact factor: 4.132

4.  Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome.

Authors:  M Schmidt; A Certoma; D Du Sart; P Kalitsis; M Leversha; K Fowler; L Sheffield; I Jack; D M Danks
Journal:  Hum Genet       Date:  1990-03       Impact factor: 4.132

5.  Physical and genetic mapping of polymorphic loci in Xq28 (DXS15, DXS52, and DXS134): analysis of a cosmid clone and a yeast artificial chromosome.

Authors:  R Feil; G Palmieri; M d'Urso; R Heilig; I Oberlé; J L Mandel
Journal:  Am J Hum Genet       Date:  1990-04       Impact factor: 11.025

6.  Investigation of factor VIII:C gene restriction fragment length polymorphisms and search for deletions in hemophiliac subjects in Algeria.

Authors:  K Nafa; F Meriane; A Reghis; M Benabadji; F Demenais; M Guilloud-Bataille; Y Sultan; J C Kaplan; M Delpech
Journal:  Hum Genet       Date:  1990-04       Impact factor: 4.132

7.  A highly conserved sequence on the short arm of chromosome 7 detects multiple polymorphisms.

Authors:  B Bardoni; S Guioli; E Maserati; P Maraschio; G Camerino
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

8.  Fine structure mapping of the hypoxanthine-guanine phosphoribosyltransferase (HPRT) gene region of the human X chromosome (Xq26).

Authors:  J A Nicklas; T C Hunter; J P O'Neill; R J Albertini
Journal:  Am J Hum Genet       Date:  1991-08       Impact factor: 11.025

9.  Genetic heterogeneity in X-linked hydrocephalus: linkage to markers within Xq27.3.

Authors:  L Strain; C M Gosden; D J Brock; D T Bonthron
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

10.  X-linked nephrogenic diabetes insipidus: from the ship Hopewell to RFLP studies.

Authors:  D G Bichet; G N Hendy; M Lonergan; M F Arthus; S Ligier; Z Pausova; R Kluge; H Zingg; P Saenger; E Oppenheimer
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025
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