Literature DB >> 4261629

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

M M Cohen, R G Davidson.   

Abstract

Entities:  

Mesh：

Year:  1972        PMID： 4261629      PMCID： PMC1469046          DOI： 10.1136/jmg.9.2.242

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  29 in total

1.  XXX 18-TRISOMY.

Authors:  N RICCI; L BORGATTI
Journal:  Lancet       Date:  1963-12-14       Impact factor: 79.321

2.  MULTIPLE CHROMOSOMAL ABNORMALITIES IN AN ACUTE EXACERBATION OF MYELOID LEUKAEMIA.

Authors:  J RUFFIE; J DUCOS; R BIERME; P COLOMBIES; A M SALLES-MOURLAN
Journal:  Lancet       Date:  1965-03-13       Impact factor: 79.321

3.  Double autosomal trisomy (D trisomy plus mongolism).

Authors:  K L BECKER; E C BURKE; A ALBERT
Journal:  Proc Staff Meet Mayo Clin       Date:  1963-06-05

4.  Post-mortem diagnosis of a new double-trisomy associated with cardiovascular and other anomalies.

Authors:  K H GUSTAVSON; B I IVEMARK; P ZETTERQVIST; J A BOOK
Journal:  Acta Paediatr       Date:  1962-11       Impact factor: 2.299

5.  [Double autosomal trisomy with 48 chromosomes (21 and 18)].

Authors:  J GAGNON; N KATYK-LONGTIN; J de GROOT; A BARBEAU
Journal:  Union Med Can       Date:  1961-11

6.  [Trisomy 21 associated with gonosomic mongolism].

Authors:  M T Duillo; G Serra
Journal:  Minerva Pediatr       Date:  1969-11-24       Impact factor: 1.312

7.  Double autosomal trisomy (trisomy D+G) with mosaicism.

Authors:  I H Porter; W Petersen; C D Brown
Journal:  J Med Genet       Date:  1969-09       Impact factor: 6.318

8.  [D+G trisomy in a patient with Rothmund's syndrome].

Authors:  F Koch; C Santamouris; F Ulbrich
Journal:  Z Kinderheilkd       Date:  1967

9.  Double aneuploidy: trisomy-18 and Klinefelter's syndrome.

Authors:  M M Cohen; T S Bumbalo
Journal:  Am J Dis Child       Date:  1967-04

10.  Three unusual trisomic patterns in children. Triple X plus triple E-triple X mosaic: normal XY-D trisomy mosaic; partial trisomy with E translocation.

Authors:  E Engel; J E Haddow; J F Lewis; R E Tipton; J C Overall; B J McGee; O J Levrat; M Engel-de-montmollin
Journal:  Am J Dis Child       Date:  1967-03
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  6 in total

1.  Trisomy 21 with 47,+18 lymphocyte cell line: double mitotic nondisjunction.

Authors:  M B Jenkins; R L Kriel; L Boyd; A Barnwell
Journal:  J Med Genet       Date:  1978-10       Impact factor: 6.318

2.  Turner phenotype: mosaic 45,X-47,XY, plus 18.

Authors:  A Schinzel; W Schmid; A Prader
Journal:  J Med Genet       Date:  1974-03       Impact factor: 6.318

3.  Dual diagnoses in 152 patients with Turner syndrome: Knowledge of the second condition may lead to modification of treatment and/or surveillance.

Authors:  Kelly L Jones; Erin A McNamara; Mauro Longoni; Danny E Miller; Mersedeh Rohanizadegan; Laura A Newman; Frances Hayes; Lynne L Levitsky; Betty L Herrington; Angela E Lin
Journal:  Am J Med Genet A       Date:  2018-08-06       Impact factor: 2.802

4.  Two cases of familial paracentric inversion in man associated with sex chromosome anomaly. 47,XXY,inv(5)(q21q32) and 45,X,inv(7)(q11.3q22.3).

Authors:  N Canki; B Dutrillaux
Journal:  Hum Genet       Date:  1979-04-05       Impact factor: 4.132

Review 5.  Down-Turner syndrome: case report and review.

Authors:  G J Van Buggenhout; B C Hamel; J C Trommelen; H Mieloo; D F Smeets
Journal:  J Med Genet       Date:  1994-10       Impact factor: 6.318

6.  Down-Turner Syndrome: A Case with Double Monoclonal Chromosomal Abnormality.

Authors:  Gioconda Manassero-Morales; Denisse Alvarez-Manassero; Alfredo Merino-Luna
Journal:  Case Rep Pediatr       Date:  2016-09-08
  6 in total

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