Literature DB >> 5301751

[The deletion of the short arm of chromosome 18 (18p- syndrome), apropos of a new observation].

S Gilgenkrantz, C Marchal, N Neimann.   

Abstract

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Year:  1968        PMID： 5301751

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


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  6 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.  Screening for minute deletions in patients with suspected cri-du-chat syndrome and apparently normal karyotype.

Authors:  H Hoehn; W Engel
Journal:  Humangenetik       Date:  1969-10

5.  On the localization of genes on certain autosomes of man through chromosome aberrations. 3. Exclusion of the possibility of gene assignment.

Authors:  K Bender; K Burckhardt
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
  6 in total

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