Literature DB >> 4381584

Syndrome associated with a deficiency of part of the long arm of chromosome no. 18.

J Insley.   

Abstract

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Year:  1967        PMID： 4381584      PMCID： PMC2019728          DOI： 10.1136/adc.42.222.140

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


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  1 in total

1.  [PARTIAL DELETION OF THE LONG ARMS OF THE CHROMOSOME 18].

Authors:  J DE GROUCHY; P ROYER; C SALMON; M LAMY
Journal:  Pathol Biol       Date:  1964-05
  1 in total
  15 in total

1.  An infant with dimples on both shoulders.

Authors:  Marjet A Wit; Arvid Kamps
Journal:  BMJ Case Rep       Date:  2011-10-04

2.  The cytogenetics of 90 patients with idiopathic mental retardation/malformation syndromes and of 90 normal subjects.

Authors:  C T Doyle
Journal:  Hum Genet       Date:  1976-07-27       Impact factor: 4.132

Review 3.  [Ring chromosome 18. 18p-/18q- -deletion-syndrome].

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

Review 4.  Partial monosomies 18. Review of cytogenetical and phenotypical variants.

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

Review 5.  Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

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

6.  Deletion of the long arms of chromosome 18 (46,XX,18q-) associated with absence of IgA and hypothyroidism in an adult.

Authors:  M J Faed; R Whyte; C R Paterson; M McCathie; J Robertson
Journal:  J Med Genet       Date:  1972-03       Impact factor: 6.318

7.  Letter: Acromial dimples: a benign familial trait.

Authors:  J W Bianchine
Journal:  Am J Hum Genet       Date:  1974-05       Impact factor: 11.025

8.  The syndrome associated with the partial deletion of the long arms of chromosome 18 (18q-).

Authors:  C E Parker; J Mavalwala; R Koch; A Hatashita; A Derencsenyi
Journal:  Calif Med       Date:  1972-10

9.  Gene deletion and duplication effects on phenotype and gamma globulin levels.

Authors:  N L Rudd; P H Lamarche
Journal:  J Med Genet       Date:  1971-03       Impact factor: 6.318

10.  Structural aberrations of chromosome 18. II. The 18q- syndrome. Report of three cases.

Authors:  A Schinzel; K Hayashi; W Schmid
Journal:  Humangenetik       Date:  1975
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