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43. The Prader-Willi syndrome: a study of 40 patients and a review of the literature. Bray GA; Dahms WT; Swerdloff RS; Fiser RH; Atkinson RL; Carrel RE Medicine (Baltimore); 1983 Mar; 62(2):59-80. PubMed ID: 6338343 [TBL] [Abstract][Full Text] [Related]
44. Tandem duplication (5q13 to 22) in a mentally deficient girl. Kessel E; Pfeiffer RA Hum Genet; 1979 Nov; 52(2):217-20. PubMed ID: 511177 [TBL] [Abstract][Full Text] [Related]
46. Incidence of 15q deletions in the Angelman syndrome: a survey of twelve affected persons. Williams CA; Gray BA; Hendrickson JE; Stone JW; Cantú ES Am J Med Genet; 1989 Mar; 32(3):339-45. PubMed ID: 2786338 [TBL] [Abstract][Full Text] [Related]
47. An inherited 1;G translocation. Ebbin AJ; Wilson MG; Towner JW; Forsman I J Med Genet; 1971 Dec; 8(4):536-9. PubMed ID: 5149540 [No Abstract] [Full Text] [Related]
48. 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. Fraccaro M; Zuffardi O; Bühler E; Schinzel A; Simoni G; Witkowski R; Bonifaci E; Caufin D; Cignacco G; Delendi N Hum Genet; 1983; 64(4):388-94. PubMed ID: 6618490 [TBL] [Abstract][Full Text] [Related]
49. Cataracts with obesity, small stature, oligophrenia, and acromicria (Prader-Labhart-Willi syndrome). Vukcevich WM; Adler RI; Hornblass AH; Gombos GM Am J Ophthalmol; 1973 Feb; 75(2):258-60. PubMed ID: 4266783 [No Abstract] [Full Text] [Related]
50. Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndrome. Clayton-Smith J; Webb T; Cheng XJ; Pembrey ME; Malcolm S J Med Genet; 1993 Jun; 30(6):529-31. PubMed ID: 8326502 [TBL] [Abstract][Full Text] [Related]
51. Weight control of children with Prader-Willi syndrome. Pipes PL; Holm VA J Am Diet Assoc; 1973 May; 62(5):520-4. PubMed ID: 4698198 [No Abstract] [Full Text] [Related]
52. [Waardenburg's syndrome and extra chromosome fragment. Study of a family]. Cordier J; Raspiller A; Gilgenkrantz S Bull Mem Soc Fr Ophtalmol; 1972; 85(0):70-81. PubMed ID: 4671855 [No Abstract] [Full Text] [Related]
54. Autosomal deletion syndrome 46,XX,18p-: a new case report with absence of IgA in serum. Fischer P; Golob E; Friedrich F; Kunze-Mühl E; Doleschel W; Aichmair H J Med Genet; 1970 Mar; 7(1):91-8. PubMed ID: 5480972 [No Abstract] [Full Text] [Related]
55. Unbalanced X-autosomal translocation with inactivation of the normal X chromosome. Mikkelsen M; Dahl G Cytogenet Cell Genet; 1973; 12(5):357-66. PubMed ID: 4131091 [No Abstract] [Full Text] [Related]
56. A chromosome survey of a hospital for the mentally subnormal. 1. Sex chromosome abnormalities. Newton MS; Jacobs PA; Price WH; Woodcock G; Fraser IA Clin Genet; 1972; 3(4):215-25. PubMed ID: 5054318 [No Abstract] [Full Text] [Related]
57. Clinical and molecular analysis of five inv dup(15) patients. Robinson WP; Binkert F; Giné R; Vazquez C; Müller W; Rosenkranz W; Schinzel A Eur J Hum Genet; 1993; 1(1):37-50. PubMed ID: 8069650 [TBL] [Abstract][Full Text] [Related]
58. Prader-Willi syndrome. A resumé of 32 cases including an instance of affected first cousins, one of whom is of normal stature and intelligence. Hall BD; Smith DW J Pediatr; 1972 Aug; 81(2):286-93. PubMed ID: 5042487 [No Abstract] [Full Text] [Related]
59. The Prader-Willi syndrome with a 15/15 translocation. Case report and review of the literature. Hawkey CJ; Smithies A J Med Genet; 1976 Apr; 13(2):152-7. PubMed ID: 933113 [TBL] [Abstract][Full Text] [Related]
60. A child with multiple congenital malformations and a 46,XX,t(Bq+;Dq-)-45,XX,-B,-D,+der(B),t(Bq+;Dq-) karyotype. Carnevale A; De los Cobos L J Med Genet; 1973 Dec; 10(4):376-9. PubMed ID: 4359604 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]