Literature DB >> 7129418

Partial Turner's syndrome in four girls with Xq duplication and Xp deficiency.

L B Nielsen, K Boczkowski, M Mikkelsen, G Dahl, E Andersen.   

Abstract

Four girls with some clinical symptoms of Turner's syndrome had Xq duplication and Xp deficiency, their karyotypes being 46,X,dup(X)(p113;q11), 46,X,dup(X)(p212;q211), 46,X,dup(X)(p225;q13), and 46,X,dup(X)(p222;q213). No mosaicism was found. The major clinical findings, short stature, lack of pterygium colli, and no continuous gamete production, are compared with those in three previously published cases.

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Year:  1982        PMID: 7129418     DOI: 10.1007/bf00291323

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  20 in total

1.  High resolution of human chromosomes.

Authors:  J J Yunis
Journal:  Science       Date:  1976-03-26       Impact factor: 47.728

2.  45,XO Turner's syndrome without evidence of mosaicism in a patient with two pregnancies.

Authors:  J Philip; V Sele
Journal:  Acta Obstet Gynecol Scand       Date:  1976       Impact factor: 3.636

3.  Identification of human chromosomes by DNA-binding fluorescent agents.

Authors:  T Caspersson; L Zech; C Johansson; E J Modest
Journal:  Chromosoma       Date:  1970       Impact factor: 4.316

4.  X-X translocation in a patient with Turner's syndrome.

Authors:  H Van den Berghe; J P Fryns; C Soyez
Journal:  Humangenetik       Date:  1973-12-20

5.  A simplified method of demonstrating Giemsa-band pattern in human chromosomes.

Authors:  J P Chaudhuri; W Vogel; I Voiculescu; U Wolf
Journal:  Humangenetik       Date:  1971

6.  Evidence for X-X chromosome translocation in humans.

Authors:  A K Sinha; J J Nora
Journal:  Ann Hum Genet       Date:  1969-10       Impact factor: 1.670

7.  A new case of Y to X translocation in a female.

Authors:  T Hecht; H J Cooke; M Cerrillo; B Meer; G Reck; H Hameister
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

8.  [Four new cases of X-autosome translocation in man (author's transl)].

Authors:  C Laurent; M C Biemont; B Dutrillaux
Journal:  Humangenetik       Date:  1975

9.  Structure and Barr body formation of an Xp + chromosome with two inactivation centers.

Authors:  R F Daly; K Patau; E Therman; G E Sarto
Journal:  Am J Hum Genet       Date:  1977-01       Impact factor: 11.025

10.  A duplication-deficiency X chromosome in a girl with severe mental retardation.

Authors:  N Sacchi; L Dalprà; E Kehyayan
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

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  3 in total

1.  A duplication/deficient X chromosome in a girl with mental retardation and dysmorphic features.

Authors:  I C Barnes; D Curtis; S L Duncan
Journal:  J Med Genet       Date:  1988-04       Impact factor: 6.318

2.  A familial Xp+ chromosome, dup (Xq26.3-->qter).

Authors:  A I Vasquez; H Rivera; L Bobadilla; J A Crolla
Journal:  J Med Genet       Date:  1995-11       Impact factor: 6.318

3.  Height of females with pure gonadal dysgenesis and normal male or female karyotype.

Authors:  K Boczkowski
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

  3 in total

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