Literature DB >> 4763942

De novo translocation t(Yq-; 15p+) in a malformed boy.

R A Pfeiffer, L Bier, F Majewski, K Rager.   

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Year:  1973        PMID： 4763942     DOI： 10.1007/bf00278418

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


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  13 in total

1.  [KLINEFELTER'S SYNDROME IN A HYPOSPADIC INFANT. KARYOTYPE WITH 46 CHROMOSOMES].

Authors:  J DE GROUCHY; N JOSSO; M LAMY; J FREZAL; C NEZELOF; G FEINTUCH
Journal:  Ann Pediatr (Paris)       Date:  1963-04-02

2.  A satellited human Y chromosome: an evidence of autosome gonosome translocation. A preliminary note.

Authors:  P Genest; M Bouchard; J Bouchard
Journal:  Can J Genet Cytol       Date:  1967-09

3.  Quinacrine mustard fluorescence of a second Y chromosome in a Y-autosomal translocation.

Authors:  S Fründ; T Koske-Westphal; S Fuchs-Mecke; E Passarge
Journal:  Humangenetik       Date:  1972

4.  A strongly fluorescing abnormal chromosome in a malformed child.

Authors:  E M Bühler; H Müller; G R Stalder; E Werder
Journal:  Humangenetik       Date:  1971

5.  Localization of male determining factor on short arm of Y chromosome. Case report of a baby with 46, x, t (Yp+;14q-).

Authors:  E Krmpotic; K Szego; R Modestas; G B Molabola
Journal:  Clin Genet       Date:  1972       Impact factor: 4.438

6.  Y-22 translocation in a YY male.

Authors:  C Lundsteen; J Philip
Journal:  Cytogenet Cell Genet       Date:  1973

7.  Satellites on the long Y chromosome arm: a familial Y-autosome translocation in man.

Authors:  W Schmid
Journal:  Cytogenetics       Date:  1969

8.  A presumptive Y-autosome translocation in a boy with congenital malformations.

Authors:  Y Nakagome; H D Smith; S W Soukup
Journal:  Am J Dis Child       Date:  1968-08

9.  Hypogonadism associated with chromosomal break in autosome no. 2 and translocation presumably on the Y chromosome.

Authors:  H Van den Berghe; O Steeno; H Verresen; P De Moor
Journal:  J Clin Endocrinol Metab       Date:  1965-09       Impact factor: 5.958

10.  [A case of primary amenorrhea with predominant Y-D translocation].

Authors:  M C Sa; L S Botelho
Journal:  Rev Iber Endocrinol       Date:  1968 Jul-Aug
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  9 in total

1.  [Mitotic and meiotic analysis of an Y-autosome translocation(author's transl)].

Authors:  B Dutrillaux; J Gueguen
Journal:  Humangenetik       Date:  1975

2.  Translocation of a supernumerary Y to a 15: study of six cases (three males and three females) in three generations.

Authors:  J Benitez; L Rivera; C Ramos; E Tejedor; A Sanchez-Cascos
Journal:  Hum Genet       Date:  1979-04-27       Impact factor: 4.132

3.  Robertsonian translocation between the chromosome Y and 15.

Authors:  I Subrt; B Blehová
Journal:  Humangenetik       Date:  1974

Review 4.  Localisation of male determining factors in man: a thorough review of structural anomalies of the Y chromosome.

Authors:  R M Davis
Journal:  J Med Genet       Date:  1981-06       Impact factor: 6.318

5.  An azoospermic male with a Y/autosome translocation.

Authors:  I Lopez Pajares; A Delicado; P V Cobos; F Sanchez Corral; C Cuadrado
Journal:  Hum Genet       Date:  1979-01-25       Impact factor: 4.132

6.  Mitotic and meiotic analysis of a reciprocal translocation t(Y;3) in an azoospermic male.

Authors:  J Gonzales; S Lesourd; B Dutrillaux
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

Review 7.  Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors:  M G Mattei; N Souiah; J F Mattei
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

8.  Prenatal diagnosis of a de novo Y/22 translocation.

Authors:  M Verjaal; P E Treffers; Y Nagal; N J Leschot
Journal:  J Med Genet       Date:  1978-12       Impact factor: 6.318

9.  Mosaicism presumably related to a Y/6 translocation in a boy with multiple congenital abnormalities.

Authors:  L Wisniewski; J V Higgins
Journal:  J Med Genet       Date:  1977-10       Impact factor: 6.318
  9 in total

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