Literature DB >> 72821

15/15 translocation in Prader-Willi syndrome.

M Fraccaro, O Zuffardi, E M Buhler, L P Jurik.   

Abstract

Two further cases (one previously published as D/D translocation) of 15/15 translocation in Prader-Willi syndrome are reported, which brings the total cases of this specific chromosomal anomaly in connection with this specific syndrome up to three or possibly four. It is suggested that Prader-Willi syndrome might be caused by loss of short arm material of chromosome 15.

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Year:  1977        PMID： 72821      PMCID： PMC1013583          DOI： 10.1136/jmg.14.4.275

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


  4 in total

1.  [Chromosomal translocation in a mentally deficient child with cryptorchidism].

Authors:  E M BUHLER; R ROSSIER; I BODIS; V VULLIET; U K BUHLER; G STALDER
Journal:  Acta Paediatr       Date:  1963-03       Impact factor: 2.299

2.  The Prader-Willi syndrome with a 15/15 translocation. Case report and review of the literature.

Authors:  C J Hawkey; A Smithies
Journal:  J Med Genet       Date:  1976-04       Impact factor: 6.318

3.  Quinacrine fluorescence patterns in somatic chromosomes of a t(15q15q) carrier.

Authors:  M C Yoshida; N Nomoto; M Sasaki
Journal:  Humangenetik       Date:  1972

4.  Translocation between both members of chromosome pair number 15 causing recurrent abortions.

Authors:  M Lucas
Journal:  Ann Hum Genet       Date:  1969-05       Impact factor: 1.670
  4 in total
  16 in total

1.  Dicentric Robertsonian translocation in man. 17 cases studied by R,C, and N banding.

Authors:  M G Mattei; J F Mattei; S Ayme; F Giraud
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

2.  Advantages of silver staining in seven rearrangements of acrocentric chromosomes, excluding Robertsonian translocations.

Authors:  M G Mattei; J F Mattei; I Vidal; F Giraud
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

3.  Anaesthetic considerations in the Prader-Willi syndrome: report of four cases.

Authors:  M Yamashita; K Koishi; R Yamaya; T Tsubo; A Matsuki; T Oyama
Journal:  Can Anaesth Soc J       Date:  1983-03

4.  Chromosome 15 in floppy infants.

Authors:  A C Berry; A J Whittingham; B G Neville
Journal:  Arch Dis Child       Date:  1981-11       Impact factor: 3.791

5.  Sudden cardiac death in a child affected by Prader-Willi syndrome.

Authors:  Cristoforo Pomara; Stefano D'Errico; Irene Riezzo; Gian Pio de Cillis; Vittorio Fineschi
Journal:  Int J Legal Med       Date:  2005-03-05       Impact factor: 2.686

Review 6.  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

7.  A girl with the Prader-Willi syndrome and Robertsonian translocation 45,XX,t(14;15)(p11;q11) which was present in three normal family members.

Authors:  A Smith; M Noel
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

8.  Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment.

Authors:  M Fraccaro; O Zuffardi; E Bühler; A Schinzel; G Simoni; R Witkowski; E Bonifaci; D Caufin; G Cignacco; N Delendi
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

9.  Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 cases.

Authors:  J F Mattei; M G Mattei; F Giraud
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

10.  An extra idic(15p)(q11) chromosome in Prader-Willi syndrome.

Authors:  H Fujita; Y Sakamoto; Y Hamamoto
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132
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