Literature DB >> 5585063

Deletion of short arm of a chromosome 18 (46, XX, 18 p-).

H Reinwein, H Ritter, U Wolf.   

Abstract

Mesh：

Year:  1967        PMID： 5585063     DOI： 10.1007/BF00286215

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


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  9 in total

1.  PROBABLE DELETION OF THE SHORT ARM OF CHROMOSOME 18.

Authors:  H E VANDYKE; A VALDMANIS; J D MANN
Journal:  Am J Hum Genet       Date:  1964-09       Impact factor: 11.025

2.  DELETION OF THE SHORT ARM OF CHROMOSOME 18.

Authors:  R L SUMMITT
Journal:  Cytogenetics       Date:  1964

3.  FAMILIAL SHORT ARM DEFICIENCY OF CHROMOSOME 18 CONCOMITANT WITH ARHINENCEPHALY AND ALOPECIA CONGENITA.

Authors:  I A UCHIDA; K N MCRAE; M RAY
Journal:  Am J Hum Genet       Date:  1965-09       Impact factor: 11.025

4.  [Deletion of the short arms of chromosome 17-18: complex deformities with oligophrenia].

Authors:  S THIEFFRY; M ARTHUIS; M LAMY; C SALMON
Journal:  Arch Fr Pediatr       Date:  1963 Jun-Jul

5.  [On a case of partial deletion of the short arm of chromosome 18, resulting in a familial 18c-17 translocation].

Authors:  J Lejeune; R Berger; M O Rethoré; P Paolini; J Boisse; P Mozziconacci
Journal:  Ann Genet       Date:  1966

6.  [Deletion of the short arm of chromosome 18].

Authors:  J de Grouchy; J Bonnette; C Salmon
Journal:  Ann Genet       Date:  1966

7.  Deletion on long arm of a chromosome 18 (46, XX, 18 q-).

Authors:  U Wolf; H Reinwein; L Z Gorman; W Künzer
Journal:  Humangenetik       Date:  1967-11-29

8.  Short arm deletions in group E and chromosomal "deletion" syndromes.

Authors:  B R Migeon
Journal:  J Pediatr       Date:  1966-09       Impact factor: 4.406

9.  [Deletion of the short arms of chromosome No. 18].

Authors:  R A Pfeiffer
Journal:  Humangenetik       Date:  1966
  9 in total
  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.  Immunological profile in a chromosome 18 deletion syndrome with IgA deficiency.

Authors:  S C Finley; M D Cooper; W H Finley; I A Uchida; T A Noto; R F Roddam
Journal:  J Med Genet       Date:  1969-12       Impact factor: 6.318

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.  Absent IgA and deletions of chromosome 18.

Authors:  J M Stewart; S Go; E Ellis; A Robinson
Journal:  J Med Genet       Date:  1970-03       Impact factor: 6.318
  6 in total

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