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28. Genetic heterogeneity of the ichthyosis, hypogonadism, mental retardation, and epilepsy syndrome. Clinical and biochemical investigations on two patients with Rud syndrome and review of the literature. Münke M; Kruse K; Goos M; Ropers HH; Tolksdorf M Eur J Pediatr; 1983 Oct; 141(1):8-13. PubMed ID: 6580169 [TBL] [Abstract][Full Text] [Related]
29. A syndrome of congenital ichthyosis, hypogonadism, small stature, facial dysmorphism, scoliosis and myogenic dystrophy. Stoll C; Eyer D Ann Genet; 1999; 42(1):45-50. PubMed ID: 10214507 [TBL] [Abstract][Full Text] [Related]
30. 46 3q+ karyotype presenting as syndrome with obesity and hypogonadism. Raman PG; Shende A; Chakraborty D; Akolekar SS J Assoc Physicians India; 2001 Apr; 49():481-4. PubMed ID: 11762626 [No Abstract] [Full Text] [Related]
31. [Sjögren-Larsson syndrome. Study of 2 cases]. Cabezuelo-Huerta G; Mulas F; Frontera-Izquierdo P An Esp Pediatr; 1983 May; 18(5):399-402. PubMed ID: 6614675 [TBL] [Abstract][Full Text] [Related]
32. Rud syndrome: congenital ichthyosis, hypogonadism, mental retardation, retinitis pigmentosa and hypertrophic polyneuropathy. Larbrisseau A; Carpenter S Neuropediatrics; 1982 May; 13(2):95-8. PubMed ID: 6182503 [TBL] [Abstract][Full Text] [Related]
33. [Ichthyosis, epileptic crises and infantilism: 4 cases of Rud syndrome]. Rodríguez Sánchez MD; Corral Caramés MJ; Rodríguez Arnao MD; Lorenzo Navarro L; Mancheño Rico E; Pérez Sotelo M An Esp Pediatr; 1986 Sep; 25(3):201-3. PubMed ID: 3789553 [TBL] [Abstract][Full Text] [Related]
37. Dermatoglyphics in Börjeson-Forssman-Lehmann syndrome. Flannery DB; Piussan C; Wright LE Am J Med Genet; 1985 Jun; 21(2):401-4. PubMed ID: 4014320 [No Abstract] [Full Text] [Related]
38. [Familial study of patients with psychosis, epilepsy and mental retardation]. Liu XH Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1983 Apr; 16(2):99-102. PubMed ID: 6617371 [No Abstract] [Full Text] [Related]
39. [Congenital hydrocephalus, oligophrenia, dwarfism, centripetal obesity and hypogonadism; an X-linked recessive hereditary illness?]. Sengers RC; Hamel BC; Otten BJ; van Gils JF; de Pagter AG Tijdschr Kindergeneeskd; 1985 Feb; 53(1):31-4. PubMed ID: 4039476 [TBL] [Abstract][Full Text] [Related]