Literature DB >> 4272425

A double chromosomal aberration of the 47, XX, 21+-47, XXp-q-, 21+ type in a girl with features of Down's and Turner's syndromes.

A V Mikel'saar, M G Blyumina, L I Kuznetsova, R V Mikel'saar, I V Lur'e.   

Abstract

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Year:  1971        PMID： 4272425

Source DB:  PubMed          Journal:  Sov Genet        ISSN： 0038-5409


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  3 in total

1.  Down and Turner syndromes in a female infant with 47,X,del(X)(p11),+21.

Authors:  J T Martsolf; M Ray; F Bauder; R Boychuk; J D Armstrong
Journal:  Hum Genet       Date:  1977-11-02       Impact factor: 4.132

2.  Down's/Turner's mosaicism. Double aneuploidy as a rare cause of missed prenatal diagnosis of chromosomal abnormality.

Authors:  R MacFaul; T Turner; M K Mason
Journal:  Arch Dis Child       Date:  1981-12       Impact factor: 3.791

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
  3 in total

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