Literature DB >> 4135076

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

A Schinzel, W Schmid, A Prader.   

Abstract

Mesh：

Year:  1974        PMID： 4135076      PMCID： PMC1013096          DOI： 10.1136/jmg.11.1.101

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


× No keyword cloud information.
  11 in total

1.  A rapid banding technique for human chromosomes.

Authors:  M Seabright
Journal:  Lancet       Date:  1971-10-30       Impact factor: 79.321

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.  Secondary nondisjunction causing regular trisomy 21 in the offspring of a mosaic trisomy 21 mother.

Authors:  E Krmpotic; M B Hardin
Journal:  Am J Obstet Gynecol       Date:  1971-06-15       Impact factor: 8.661

4.  Paternal trisomy 21 mosaicism and Down's syndrome.

Authors:  L Y Hsu; M Gertner; E Leiter; K Hirschhorn
Journal:  Am J Hum Genet       Date:  1971-11       Impact factor: 11.025

5.  Sex chromatin in hair roots.

Authors:  W Schmid
Journal:  Cytogenetics       Date:  1967

6.  [Mosaicism 45, X-47, XY,+21].

Authors:  M Prieur; B Dutrillaux; S Carpentier; R Berger; O Raoul; M O Rethoré; J Lejeune
Journal:  Ann Genet       Date:  1972-09

7.  Parental mosaicism in trisomy 18.

Authors:  N G Beratis; N B Kardon; L Y Hsu; D Grossman; K Hirschhorn
Journal:  Pediatrics       Date:  1972-12       Impact factor: 7.124

8.  Turner's syndrome in one of monozygotic twins with mosaicism.

Authors:  A M Potter; L S Taitz
Journal:  Acta Paediatr Scand       Date:  1972-07

9.  Analysis of human metaphase chromosome set by aid of DNA-binding fluorescent agents.

Authors:  T Caspersson; L Zech; C Johansson
Journal:  Exp Cell Res       Date:  1970-10       Impact factor: 3.905

10.  [Sex chromatine determination from roots of hair].

Authors:  W Schmid
Journal:  Experientia       Date:  1967-04-15
View more
  8 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.  Tissue-specific 45,X0/47,XY,+13 mosaicism in an 18-year-old woman.

Authors:  B Eiben; S Hansen; R Goebel; W Hammans
Journal:  Hum Genet       Date:  1989-07       Impact factor: 4.132

3.  A case of Turner's syndrome, with apparently normal sex chromatin and chromosome findings.

Authors:  M G Butler; C T Todd; J D Eisen
Journal:  Nebr Med J       Date:  1979-05

4.  Cytogenetic findings in 89 cases of Turner's syndrome with abnormal karyotypes.

Authors:  W Schmid; E Naef; G Mürset; A Prader
Journal:  Humangenetik       Date:  1974

5.  Mosaic 45,x/47,xy,+18.

Authors:  F Serville; D Fontan; C Laurent; J M Cazauran; P Verger
Journal:  Hum Genet       Date:  1977-05-10       Impact factor: 4.132

6.  The phenotype Ae1B: a probable result of chimerism.

Authors:  G H Longster; E A Robinson; D I North
Journal:  J Med Genet       Date:  1978-10       Impact factor: 6.318

7.  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

8.  Aberrant melanoblast migration associated with trisomy 18 mosaicism.

Authors:  J Chemke; S Rappaport; R Etrog
Journal:  J Med Genet       Date:  1983-04       Impact factor: 6.318
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.