Literature DB >> 4768115

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

H Van den Berghe, J P Fryns, C Soyez.   

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Year:  1973        PMID: 4768115     DOI: 10.1007/bf00273343

Source DB:  PubMed          Journal:  Humangenetik        ISSN: 0018-7348


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  8 in total

1.  A VERY LARGE METACENTRIC CHROMOSOME IN A WOMAN WITH SYMPTOMS OF TURNER'S SYNDROME.

Authors:  G WIELIE; J M COENEGRACHT; G STALDER
Journal:  Cytogenetics       Date:  1964

2.  Gonadal Dysgenesis with Unusual Abnormalities.

Authors:  K Hugh-Jones; S J Wallace; J M Thornber; N B Atkin
Journal:  Arch Dis Child       Date:  1965-06       Impact factor: 3.791

3.  An abnormal large human chromosome identified as an end-to-end fusion of two X's by combined results of the new banding techniques and microdensitometry.

Authors:  C Distèche; A Hagemeijer; J Frederic; D Progneaux
Journal:  Clin Genet       Date:  1972       Impact factor: 4.438

4.  [Gonadal dysgenesis with an unusual structural anomaly in an X chromosome (45,X-46,XXq+)].

Authors:  A Dollmann; W Nocke; S Stengel-Rutkowski
Journal:  Humangenetik       Date:  1972

5.  Multiple abnormalities due to possible genetic inactivation in an X-autosome translocation.

Authors:  T H Thelen; D J Abrams; R O Fisch
Journal:  Am J Hum Genet       Date:  1971-07       Impact factor: 11.025

6.  [Duplication of an X chromosome in a case of Turner's syndrome (45,X-46,XXp+)].

Authors:  I Emerit; J German; L P Crippa; C Sureau
Journal:  Ann Genet       Date:  1970-12

7.  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

8.  X inactivation in man: a woman with t(Xq--;12q+).

Authors:  G E Sarto; E Therman; K Patau
Journal:  Am J Hum Genet       Date:  1973-05       Impact factor: 11.025

  8 in total
  7 in total

1.  A girl with an end-to-end fusion of two X'S.

Authors:  C Stoll; C Lausecker; A Pennerath
Journal:  Eur J Pediatr       Date:  1979-05-18       Impact factor: 3.183

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

Authors:  L B Nielsen; K Boczkowski; M Mikkelsen; G Dahl; E Andersen
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

3.  Cytogenetic and clinical studies in gonadal dysgenesis with 46,X,Xt(qter leads to p221::p223 leads to qter) karyotype: review and phenotype/karyotype correlations.

Authors:  M Ferraro; A De Capoa; C Mostacci; F Pelliccia; P Zulli; M A Baldini; Q Di Nisio
Journal:  J Med Genet       Date:  1980-12       Impact factor: 6.318

4.  Cytological findings of 10 cases with i(Xq) and one with dic(X)(qter leads to cen leads to p22::p11 leads to qter).

Authors:  H Fujita; Y Tanigawa; Y Yoshida; Y Okada
Journal:  Hum Genet       Date:  1977-11-10       Impact factor: 4.132

5.  Differences in human X isochromosomes.

Authors:  J H Priest; R D Blackston; K S Au; S L Ray
Journal:  J Med Genet       Date:  1975-12       Impact factor: 6.318

6.  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

7.  X-X translocation in a patient with gonadal dysgenesis and the problems of phenotype-karyotype correlations.

Authors:  G G Mirzayants; L I Baranovskaya
Journal:  Hum Genet       Date:  1978-02-16       Impact factor: 4.132

  7 in total

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