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2. [Idiopathic multicentric osteolysis with craniodysplasis and mental retardation: a new syndrome? (author's transl)]. Mathias K; Ludwig U Rofo; 1977 Sep; 127(3):255-61. PubMed ID: 143430 [TBL] [Abstract][Full Text] [Related]
3. The radiology of Coffin-Lowry syndrome. Padley S; Hodgson SV; Sherwood T Br J Radiol; 1990 Jan; 63(745):72-5. PubMed ID: 2306591 [No Abstract] [Full Text] [Related]
5. 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]
6. Skeletal anomalies in genetically determined congenital heart disease. Poznanski AK; Stern AM; Gall JC Radiol Clin North Am; 1971 Dec; 9(3):435-58. PubMed ID: 5145748 [No Abstract] [Full Text] [Related]
7. [A female case of Prader and Willi syndrome; exploration at the post puberal age (author's transl)]. Schaison G; Nathan C; Gilbert-Dreyfus Ann Endocrinol (Paris); 1973; 34(3):286-8. PubMed ID: 4751204 [No Abstract] [Full Text] [Related]
8. 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]
9. [Autopsy case of hypoglycemic coma in a young diabetic woman with mental and somatic retardation (Prader-Labhart-Willi syndrome)]. Oda M; Nagashima K; Shiraki H; Nishio I; Nagata N Acta Neuropathol; 1972; 20(3):225-36. PubMed ID: 5044003 [No Abstract] [Full Text] [Related]
10. 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]
11. Hypogonadotropinism in Prader-Willi syndrome. Induction of puberty and sperm altogenesis by clomiphene citrate. Hamilton CR; Scully RE; Kliman B Am J Med; 1972 Mar; 52(3):322-9. PubMed ID: 5011391 [No Abstract] [Full Text] [Related]
12. Hunter-McAlpine syndrome: report of a third family. Adès LC; Morris LL; Simpson DA; Haan EA Clin Dysmorphol; 1993 Apr; 2(2):123-30. PubMed ID: 8281273 [TBL] [Abstract][Full Text] [Related]
13. Otospondylomegaepiphyseal dysplasia: report of three sibs and review of the literature. al Gazali LI; Lytle W Clin Dysmorphol; 1994 Jan; 3(1):46-54. PubMed ID: 8205326 [TBL] [Abstract][Full Text] [Related]
14. Radiographic manifestations of the arthrogryposis syndrome. Poznanski AK; La Rowe PC Radiology; 1970 May; 95(2):353-8. PubMed ID: 5439444 [No Abstract] [Full Text] [Related]
18. Clinical and roentgenographic findings in a patient with primordial microcephalic dwarfism type Caroline Crachami. Boscherini B; Colabucci F; Galasso C; Marietti G; Cappa M; Pasquino AM Am J Med Genet; 1996 Dec; 66(3):269-72. PubMed ID: 8985485 [TBL] [Abstract][Full Text] [Related]
19. [Rubinstein-Taybi syndrome of broad thumbs and broad big toes with cranio-mandibulo-facial malformations and mental retardation]. Weiland R Arch Kinderheilkd; 1969 May; 179(1):78-90. PubMed ID: 5799636 [No Abstract] [Full Text] [Related]
20. [Prader-Willi-Labhardt syndrome in a girl with development of an insulinoprivic diabete]. Battin J; Aubertin J; Alberty J; Fontan D Bord Med; 1970 Oct; 3(10):2462. PubMed ID: 5480225 [No Abstract] [Full Text] [Related] [Next] [New Search]