Literature DB >> 4181138

IgA absence associated with short arm deletion of chromosome No. 18.

R H Ruvalcaba, H C Thuline.   

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Year:  1969        PMID： 4181138     DOI： 10.1016/s0022-3476(69)80234-9

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


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  7 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

Review 3.  Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

Authors:  G Töndury
Journal:  Humangenetik       Date:  1973-03-23

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

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

Review 5.  Population cytogenetics, assignment of gene loci in autosomes, karyotype-phenotype correlations. A progress report on human cytogenetics.

Authors:  E Passarge
Journal:  Humangenetik       Date:  1970

6.  Autosomal deletion syndrome 46,XX,18p-: a new case report with absence of IgA in serum.

Authors:  P Fischer; E Golob; F Friedrich; E Kunze-Mühl; W Doleschel; H Aichmair
Journal:  J Med Genet       Date:  1970-03       Impact factor: 6.318

7.  Dicentric chromosome due to an unusual fusion.

Authors:  I Subrt; B Blehová; O Táborský
Journal:  Humangenetik       Date:  1971
  7 in total

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