Literature DB >> 3507285

Report of the committee on human gene mapping by recombinant DNA techniques.

P L Pearson, K K Kidd, H F Willard.   

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Year:  1987        PMID： 3507285     DOI： 10.1159/000132487

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


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  29 in total

1.  DNA analysis in Turkish Duchenne/Becker muscular dystrophy families.

Authors:  E Battaloğlu; M Telatar; F Deymeer; P Serdaroğlu; F Kuseyri; C Ozdemir; M Apak; A Tolun
Journal:  Hum Genet       Date:  1992-08       Impact factor: 4.132

2.  Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome.

Authors:  Z Rahmani; J L Blouin; N Creau-Goldberg; P C Watkins; J F Mattei; M Poissonnier; M Prieur; Z Chettouh; A Nicole; A Aurias
Journal:  Proc Natl Acad Sci U S A       Date:  1989-08       Impact factor: 11.205

3.  Germinal mosaicism increases the recurrence risk for 'new' Duchenne muscular dystrophy mutations.

Authors:  E Bakker; H Veenema; J T Den Dunnen; C van Broeckhoven; P M Grootscholten; E J Bonten; G J van Ommen; P L Pearson
Journal:  J Med Genet       Date:  1989-09       Impact factor: 6.318

4.  Maternal meiosis II nondisjunction in a case of 47,XXY testicular feminization.

Authors:  U Müller; N R Schneider; J F Marks; K G Kupke; G N Wilson
Journal:  Hum Genet       Date:  1990-02       Impact factor: 4.132

5.  Genetic mapping of two new DNA markers in Xq26-q28 relative to the fragile-X syndrome locus.

Authors:  R Sood; L M Mulligan; R Poon; B N White; J J Holden
Journal:  Am J Hum Genet       Date:  1990-09       Impact factor: 11.025

6.  Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.

Authors:  R A Lewis
Journal:  Trans Am Ophthalmol Soc       Date:  1989

7.  Linkage analysis in the spinal muscular atrophy type of facioscapulohumeral disease.

Authors:  T Siddique; H Roper; M A Pericak-Vance; J Shaw; K L Warner; W Y Hung; K L Phillips; P Lunt; W J Cumming; A D Roses
Journal:  J Med Genet       Date:  1989-08       Impact factor: 6.318

8.  TaqI RFLP identified by probe 1A1 [DXS374] at Xq28.

Authors:  G K Suthers; K E Davies; E Baker; G R Sutherland
Journal:  Nucleic Acids Res       Date:  1989-11-11       Impact factor: 16.971

9.  Isolation of chromosome-21-specific DNA probes and their use in the analysis of nondisjunction in Down syndrome.

Authors:  J Galt; E Boyd; J M Connor; M A Ferguson-Smith
Journal:  Hum Genet       Date:  1989-01       Impact factor: 4.132

Review 10.  Human chromosome 8.

Authors:  S Wood
Journal:  J Med Genet       Date:  1988-11       Impact factor: 6.318
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