Literature DB >> 14025631

XXX 21-trisomy and retinoblastoma.

R W DAY, S W WRIGHT, A KOONS, M QUIGLEY.   

Abstract

Entities:  

Keywords:  CHROMOSOMES; RETINOBLASTOMA

Mesh：

Year:  1963        PMID： 14025631     DOI： 10.1016/s0140-6736(63)92629-1

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


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  15 in total

1.  CHROMOSOME ABNORMALITIES IN NEUROBLASTOMA.

Authors:  D J BREWSTER; J V GARRETT
Journal:  J Clin Pathol       Date:  1965-03       Impact factor: 3.411

2.  Double aneuploidy (47,XX,21+-45,X) arising through simultaneous double non-disjunction.

Authors:  M M Cohen; R G Davidson
Journal:  J Med Genet       Date:  1972-06       Impact factor: 6.318

3.  XYY chromosomal complement, proven by fluorescence, in a child with trisomy 21:48,XYY,21+.

Authors:  M Osztovics; G Ivády; E M Bühler
Journal:  Humangenetik       Date:  1971

4.  A case of XYY Down's syndrome confirmed by autoradiography.

Authors:  R Laxova; J A McKeown; P Saldaña; J A Timothy
Journal:  J Med Genet       Date:  1971-06       Impact factor: 6.318

Review 5.  Down's syndrome. Current stage of cytogenetic research.

Authors:  M Mikkelsen
Journal:  Humangenetik       Date:  1971

6.  Double chromosomal aberration. Trisomy G and the balanced translocation t(3p--;17q+).

Authors:  I Subrt; H Prchliková
Journal:  Humangenetik       Date:  1969-10

7.  Karyotype studies among children with severe visual handicap.

Authors:  G R Fraser; A I Friedmann; J D Delhanty; J H Edwards; A M Glen-Bott; J Insley; K P Lele; U Mittwoch; D Mutton
Journal:  Br J Ophthalmol       Date:  1970-02       Impact factor: 4.638

8.  Dq-, Dr and retinoblastoma.

Authors:  A I Taylor
Journal:  Humangenetik       Date:  1970

9.  The triplo-X female: an appraisal based on a study of 12 cases and a review of the literature.

Authors:  M L Barr; F R Sergovich; D H Carr; E L Saver
Journal:  Can Med Assoc J       Date:  1969-09-06       Impact factor: 8.262

10.  Double autosomal trisomy and mosaicism for three cell lines in man: coexisting trisomy 13-15, trisomy 17-18, and a minority cell line trisomic for a chromosome of both groups.

Authors:  O M Garson; A G Baikie; J Ferguson; C H Greer
Journal:  J Med Genet       Date:  1969-06       Impact factor: 6.318
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