Literature DB >> 5091271

Intestinal nodular lymphoid hyperplasia, hypogammaglobulinemia, and hematologic abnormalities in a child with a ring 18 chromosome.

D L Michaels, S Go, J R Humbert, R S Dubois, J M Stewart, E F Ellis.   

Abstract

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Year:  1971        PMID： 5091271     DOI： 10.1016/s0022-3476(71)80062-8

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  5 in total

Review 1.  [Ring chromosome 18. 18p-/18q- -deletion-syndrome].

Authors:  J Kunze; E Stephan; M Tolksdorf
Journal:  Humangenetik       Date:  1972

Review 2.  Partial monosomies 18. Review of cytogenetical and phenotypical variants.

Authors:  I W Lurie; G I Lazjuk
Journal:  Humangenetik       Date:  1972

3.  Immunoglobulin abnormality in a girl with a large chromosome 18.

Authors:  S Yanagisawa
Journal:  J Med Genet       Date:  1972-09       Impact factor: 6.318

4.  An unusual inflammatory lesion of the jejunum in a patient with late onset immunoglobulin deficiency.

Authors:  S E Williams
Journal:  Postgrad Med J       Date:  1980-02       Impact factor: 2.401

5.  Nodular lymphoid hyperplasia with hypogammaglobulinaemia.

Authors:  A B Ajdukiewicz; G R Youngs; I A Bouchier
Journal:  Gut       Date:  1972-08       Impact factor: 23.059
  5 in total

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