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24. Detection of a novel familial deletion of four genes between BP1 and BP2 of the Prader-Willi/Angelman syndrome critical region by oligo-array CGH in a child with neurological disorder and speech impairment. Murthy SK; Nygren AO; El Shakankiry HM; Schouten JP; Al Khayat AI; Ridha A; Al Ali MT Cytogenet Genome Res; 2007; 116(1-2):135-40. PubMed ID: 17268193 [TBL] [Abstract][Full Text] [Related]
25. Foreign body aspiration in a boy with Prader-Willi Syndrome. Jacob SS; Jacob JJ; Paul TV Singapore Med J; 2008 Jan; 49(1):e12-4. PubMed ID: 18204752 [TBL] [Abstract][Full Text] [Related]
26. The Cohen syndrome. Fryns JP; Van den Berghe H J Genet Hum; 1981 Dec; 29(4):449-53. PubMed ID: 7328419 [TBL] [Abstract][Full Text] [Related]
27. [Report of case of Prader-Willi syndrome]. Visco G; Ughi M; Trevenzoli G Pediatr Med Chir; 1999; 21(3):149-50. PubMed ID: 10687166 [TBL] [Abstract][Full Text] [Related]
33. Duplication of proximal 15q as a cause of Prader-Willi syndrome. Pettigrew AL; Gollin SM; Greenberg F; Riccardi VM; Ledbetter DH Am J Med Genet; 1987 Dec; 28(4):791-802. PubMed ID: 3688017 [TBL] [Abstract][Full Text] [Related]
34. Pure distal monosomy 10q26 in a patient displaying clinical features of Prader-Willi syndrome during infancy and distinct behavioural phenotype in adolescence. Lukusa T; Fryns JP Genet Couns; 2000; 11(2):119-26. PubMed ID: 10893663 [TBL] [Abstract][Full Text] [Related]
35. Regional cerebral glucose metabolic abnormality in Prader-Willi syndrome: A 18F-FDG PET study under sedation. Kim SE; Jin DK; Cho SS; Kim JH; Hong SD; Paik KH; Oh YJ; Kim AH; Kwon EK; Choe YH J Nucl Med; 2006 Jul; 47(7):1088-92. PubMed ID: 16818941 [TBL] [Abstract][Full Text] [Related]
36. [Infant hypotonia, obesity, hypogenitalism and oligophrenia--new viewpoints on the etiology and symptoms of Prader-Willi syndrome]. Witkowski R; Ullrich E; Pietsch P; Weber K; Heller K; Losanowa T; Nitz I Psychiatr Neurol Med Psychol (Leipz); 1985 May; 37(5):255-61. PubMed ID: 4023109 [TBL] [Abstract][Full Text] [Related]
37. Language development in a 3-year-old boy with Prader-Willi syndrome. Atkin K; Lorch MP Clin Linguist Phon; 2007 Apr; 21(4):261-76. PubMed ID: 17453868 [TBL] [Abstract][Full Text] [Related]
38. Mental retardation, distinct facial changes, short stature, obesity, and hypogonadism: a new X-linked mental retardation syndrome. Chudley AE; Lowry RB; Hoar DI Am J Med Genet; 1988 Dec; 31(4):741-51. PubMed ID: 3239563 [TBL] [Abstract][Full Text] [Related]
39. [The hypotonia-hypomentia-hypogonadism-obesity syndrome (Prader-Willi-Labhart syndrome) in a 38-year-old man]. van Bergeijk L; van der Veen EA Ned Tijdschr Geneeskd; 1980 Dec; 124(49):2090-2. PubMed ID: 7442851 [No Abstract] [Full Text] [Related]
40. Lymphedema in Prader-Willi syndrome. Heitink MV; Sinnema M; van Steensel MA; Schrander-Stumpel CT; Frank J; Curfs LM Int J Dermatol; 2008 Nov; 47 Suppl 1():42-4. PubMed ID: 18986486 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]