Prader Willi Syndrome and Other Chromosome 15q Deletion DisordersTolmie, J. · Journal of Medical Genetics · 1993

Corrigendum: Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 151995

Molecular and clinical characterization of two patients with Prader–Willi syndrome and atypical deletions of proximal chromosome 15qGabriela Calounova; Petra Hedvicakova; Eva Silhanova; Gabriela Kreckova; Zdenek Sedlacek · 2008

Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15Buiting, Karin; Saitoh, Shinji; Gross, Stephanie; Dittrich, Bärbel; Schwartz, Stuart; Nicholls, Robert D.; Horsthemke, Bernhard · 1995

Prader–Willi Syndrome and Angelman Syndrome in Cousins from a Family with a Translocation between Chromosomes 6 and 15Smeets, Dominique F.C.M.; Hamel, Ben C.J.; Nelen, Marcel R.; Smeets, Hubertus J.M.; Bollen, Josephus H.M.; Smits, Arie P.T.; Ropers, Hans-Hilger; van Oost, Bernard A. · New England Journal of Medicine · 1992

Prenatal diagnosis of Prader–Willi syndrome and Angelman syndrome for fetuses with suspicious deletion of chromosomal region 15q11-q13Chang, Chia-Wei; Hsu, Hui-Kuo; Kao, Chiu-Ching; Huang, Jyun-Yuan; Kuo, Pao-Lin · International Journal of Gynecology & Obstetrics · 2014

Difference in methylation patterns within the D15S9 region of chromosome 15qll–13 in first cousins with Angelman syndrome and Prader–Willi syndromeDr. Jill Clayton-Smith; Daniel J. Driscoll; Michael F. Waters; Tessa Webb; Tony Andrews; Sue Malcolm; Marcus E. Pembrey; Robert D. Nicholls · 1993

A patient with Prader–Willi syndrome and a supernumerary marker chromosome r(15)(q11.1-13p11.1)pat and maternal heterodisomyMarion Werner; Ziva Ben-Neriah; Shira silverstein; Israela Lerer; Yudith Dagan; Dvorah Abeliovich · 2004

Constitutional chromosomal breakageF. Giraud; S. Ayme; J. F. Mattei; M. G. Mattei · 1976

Dicentric Robertsonian translocations in manM. G. Mattei; J. F. Mattei; S. Ayme; F. Giraud · 1979

Four new cases of dicentric Y chromosomesF. Giraud; J. F. Mattei; C. Lucas; M. G. Mattei · 1977

Origin of the extra chromosome in trisomy 21J. F. Mattei; M. G. Mattei; S. Ayme; F. Giraud · 1979

Structural anomalies of the X chromosome and inactivation centerM. G. Mattei; J. F. Mattei; I. Vidal; F. Giraud · 1981

X-Autosome translocations: Cytogenetic characteristics and their consequencesM. G. Mattei; J. F. Mattei; S. Ayme; F. Giraud · 1982

Quantitative and qualitative study of acrocentric associations in 109 normal subjectsJ. F. Mattei; S. Ayme; M. G. Mattei; J. Gouvernet; F. Giraud · 1976