Literature DB >> 365264

Chronic granulomatous disease, the McLeod syndrome, and the Kell blood groups.

W L Marsh.   

Abstract

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Year:  1978        PMID： 365264

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN： 0547-6844


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  5 in total

1.  The first report of a Chinese family with McLeod syndrome.

Authors:  Bik Ling Man; Yuet Ping Yuen; Yat Pang Fu
Journal:  BMJ Case Rep       Date:  2014-06-03

2.  Linkage of genes for chronic granulomatous disease and Xg.

Authors:  G Wolff; C R Müller; A Jobke
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

3.  Xp21 DNA microdeletion in a patient with chronic granulomatous disease, retinitis pigmentosa, and McLeod phenotype.

Authors:  G de Saint-Basile; M C Bohler; A Fischer; J Cartron; J L Dufier; C Griscelli; S H Orkin
Journal:  Hum Genet       Date:  1988-09       Impact factor: 4.132

Review 4.  McLeod syndrome: a distinct form of neuroacanthocytosis. Report of two cases and literature review with emphasis on neuromuscular manifestations.

Authors:  T N Witt; A Danek; M Reiter; M U Heim; J Dirschinger; E G Olsen
Journal:  J Neurol       Date:  1992-07       Impact factor: 4.849

5.  Chronic granulomatous disease, the McLeod phenotype and the contiguous gene deletion syndrome-a review.

Authors:  Casey E Watkins; John Litchfield; Eunkyung Song; Gayatri B Jaishankar; Niva Misra; Nikhil Holla; Michelle Duffourc; Guha Krishnaswamy
Journal:  Clin Mol Allergy       Date:  2011-11-23
  5 in total

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