Deletions of chromosome 15 as a cause of the Pr... [N Engl J Med. 1981] - PubMed

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The Prader-Willi syndrome and interstitial deletion of chromosome 15: high-resolution chromosome analyses of 14 patients with the Prader-Willi syndrome and of 5 suspected infants. [Jinrui Idengaku Zasshi. 1984]
The Prader-Willi syndrome and interstitial deletion of chromosome 15: high-resolution chromosome analyses of 14 patients with the Prader-Willi syndrome and of 5 suspected infants.
Fukushima Y, Niikawa N, Kuroki Y. Jinrui Idengaku Zasshi. 1984 Mar; 29(1):1-6.
Deletion of chromosome 15 (q11-13) in a Prader-Labhart-Willi syndrome clinic population. [Am J Med Genet. 1984]
Deletion of chromosome 15 (q11-13) in a Prader-Labhart-Willi syndrome clinic population.
Cassidy SB, Thuline HC, Holm VA. Am J Med Genet. 1984 Feb; 17(2):485-95.
Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequences. [Genomics. 1990]
Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequences.
Buiting K, Neumann M, Lüdecke HJ, Senger G, Claussen U, Antich J, Passarge E, Horsthemke B. Genomics. 1990 Mar; 6(3):521-7.
Review Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis. [Hum Genet. 1984]
Review Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.
Mattei MG, Souiah N, Mattei JF. Hum Genet. 1984; 66(4):313-34.
Review Interstitial 6q deletion with a Prader-Willi-like phenotype: a new case and review of the literature. [Eur J Paediatr Neurol. 2000]
Review Interstitial 6q deletion with a Prader-Willi-like phenotype: a new case and review of the literature.
Gilhuis HJ, van Ravenswaaij CM, Hamel BJ, Gabreëls FJ. Eur J Paediatr Neurol. 2000; 4(1):39-43.

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Cited by 65 PubMed Central articles

Prader-Willi Syndrome: Obesity due to Genomic Imprinting. [Curr Genomics. 2011]
Prader-Willi Syndrome: Obesity due to Genomic Imprinting.
Butler MG. Curr Genomics. 2011 May; 12(3):204-15.
Controlled somatic and germline copy number variation in the mouse model. [Curr Genomics. 2010]
Controlled somatic and germline copy number variation in the mouse model.
Hérault Y, Duchon A, Maréchal D, Raveau M, Pereira PL, Dalloneau E, Brault V. Curr Genomics. 2010 Sep; 11(6):470-80.
The phenotype of recurrent 10q22q23 deletions and duplications. [Eur J Hum Genet. 2011]
The phenotype of recurrent 10q22q23 deletions and duplications.
van Bon BW, Balciuniene J, Fruhman G, Nagamani SC, Broome DL, Cameron E, Martinet D, Roulet E, Jacquemont S, Beckmann JS, et al. Eur J Hum Genet. 2011 Apr; 19(4):400-8. Epub 2011 Jan 19.

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Deletions of chromosome 15 as a cause of the Prader-Willi syndrome.
Deletions of chromosome 15 as a cause of the Prader-Willi syndrome.
N Engl J Med. 1981 Feb 5 ;304(6):325-9.

PubMed
Trichinella spiralis: delayed rejection in mice concurrently infected with Nemat...
Trichinella spiralis: delayed rejection in mice concurrently infected with Nematospiroides dubius.
Exp Parasitol. 1978 Nov ;46(1):121-30.

PubMed
Rapid isolation of high molecular weight plant DNA.
Rapid isolation of high molecular weight plant DNA.
Nucleic Acids Res. 1980 Oct 10 ;8(19):4321-5.

PubMed
Epidemiology Standardization Project (American Thoracic Society).
Epidemiology Standardization Project (American Thoracic Society).
Am Rev Respir Dis. 1978 Dec ;118(6 Pt 2):1-120.

PubMed
The prepregnancy clinic.
The prepregnancy clinic.
Br Med J. 1980 Aug 30 ;281(6240):619.

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