Literature DB >> 4170757

Partial E-18 long-arm deletion.

W E Nance, S H Higdon, B Chown, E Engel.   

Abstract

Mesh:

Year:  1968        PMID: 4170757     DOI: 10.1016/s0140-6736(68)90155-4

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


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  12 in total

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

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

Review 3.  Partial monosomies 18. Review of cytogenetical and phenotypical variants.

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

Review 4.  Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

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

5.  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

6.  Partial deletion of the long arm of chromosome 18.

Authors:  A V Mikelsaar; T A Talvik
Journal:  Humangenetik       Date:  1969

7.  E ring chromosome with persistent left superior vena cava and hypertrophic subaortic stenosis.

Authors:  S Wald; E Engel; W E Nance; J Davies; F A Puyau; B C Sinclair-Smith
Journal:  J Med Genet       Date:  1969-09       Impact factor: 6.318

8.  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

9.  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

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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