Literature DB >> 7305434

Chromosome 15 in floppy infants.

A C Berry, A J Whittingham, B G Neville.   

Abstract

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Year:  1981        PMID： 7305434      PMCID： PMC1627383          DOI： 10.1136/adc.56.11.882

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


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  10 in total

1.  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

2.  [A jumping translocation (5p;15q), (8q;15q), and (12q;15q) (author's transl)].

Authors:  J Lejeune; C Maunoury; M Prieur; J Van den Akker
Journal:  Ann Genet       Date:  1979

3.  The Prader-Willi syndrome with a 15/3 translocation.

Authors:  M Kucerová; M Straková; Z Polívková
Journal:  J Med Genet       Date:  1979-06       Impact factor: 6.318

4.  Robertsonian translocation between the chromosome Y and 15.

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

5.  [The Prader-Willi syndrome and 15-15 translocation].

Authors:  J M Emberger; M Rodiere; J Astruc; D Brunel
Journal:  Ann Genet       Date:  1977-12

6.  Fusion of homologous chromosomes (15q15q) as cause of recurrent abortion.

Authors:  M Bartsch-Sandhoff
Journal:  Lancet       Date:  1977-03-05       Impact factor: 79.321

7.  15/15 translocation in Prader-Willi syndrome.

Authors:  M Fraccaro; O Zuffardi; E M Buhler; L P Jurik
Journal:  J Med Genet       Date:  1977-08       Impact factor: 6.318

8.  Deletions of chromosome 15 as a cause of the Prader-Willi syndrome.

Authors:  D H Ledbetter; V M Riccardi; S D Airhart; R J Strobel; B S Keenan; J D Crawford
Journal:  N Engl J Med       Date:  1981-02-05       Impact factor: 91.245

9.  Prader-Willi syndrome and a bisatellited derivative of chromosome 15.

Authors:  L P Wisniewski; M E Witt; F Ginsberg-Fellner; J Wilner; R J Desnick
Journal:  Clin Genet       Date:  1980-07       Impact factor: 4.438

10.  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
  10 in total
  8 in total

1.  Derivative Y chromosome resulting from a t(Y;15) (q12;q11.2) in a boy with Prader-Willi syndrome.

Authors:  Y Suzuki; I Sasagawa; T Sawamura; M Ishigooka; H Kaneko; Y Kubota; T Nakada
Journal:  Int Urol Nephrol       Date:  1996       Impact factor: 2.370

2.  A male with a de novo translocation involving loss of 15q11q13 material and Prader-Willi syndrome.

Authors:  S Vickers; M Dahlitz; C Hardy; M Kilpatrick; T Webb
Journal:  J Med Genet       Date:  1994-06       Impact factor: 6.318

Review 3.  Microdeletion syndromes, balanced translocations, and gene mapping.

Authors:  A Schinzel
Journal:  J Med Genet       Date:  1988-07       Impact factor: 6.318

Review 4.  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

5.  Cytogenetic studies of familial Prader-Willi syndrome.

Authors:  T Hasegawa; M Hara; M Ando; M Osawa; Y Fukuyama; M Takahashi; K Yamada
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

6.  Unbalanced reciprocal translocations in cases of Prader-Willi syndrome.

Authors:  D P Duckett; S H Roberts; P Davies
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

7.  Prader-Willi syndrome: current understanding of cause and diagnosis.

Authors:  M G Butler
Journal:  Am J Med Genet       Date:  1990-03

8.  Chromosome 15 in Prader-Willi syndrome.

Authors:  C N Fear; D E Mutton; A C Berry; J Z Heckmatt; V Dubowitz
Journal:  Dev Med Child Neurol       Date:  1985-06       Impact factor: 5.449
  8 in total

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