These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
98 related articles for article (PubMed ID: 5617749)
21. Albinism and schizophreniform psychosis: a pedigree study. Baron M Am J Psychiatry; 1976 Sep; 133(9):1070-3. PubMed ID: 961931 [TBL] [Abstract][Full Text] [Related]
22. Presumed homozygous Ehlers-Danlos syndrome type I in a highly inbred kindred. Kozlova SI; Prytkov AN; Blinnikova OE; Sultanova FA; Bochkova DN Am J Med Genet; 1984 Aug; 18(4):763-7. PubMed ID: 6237581 [TBL] [Abstract][Full Text] [Related]
23. Unusual combination of genetic defects in a Sicilian boy: G gamma delta beta thalassemia, G gamma A gamma heterocellular HPFH, beta (0) thalassemia, and albinism. Schilirò G; Pavone L; Romeo MA; Russo A; Musumeci S; Russo G Am J Med Genet; 1983 Jun; 15(2):225-31. PubMed ID: 6192718 [TBL] [Abstract][Full Text] [Related]
24. [Hereditary epidermolysis bullosa in Tunisia: an epidemio-clinical and ultrastructural study]. Cherif F; Mnajja N; Feriani S; Ben Saïd ZM; Jaafoura MH; Dhahri AB; Boubaker S Arch Inst Pasteur Tunis; 2005; 82(1-4):53-8. PubMed ID: 16929755 [TBL] [Abstract][Full Text] [Related]
25. Inborn errors of lipid metabolism coincidence of hyperlipoproteinaemia type 3 and albinism. Sobra J; Jílek M Rev Czech Med; 1971; 17(4):214-8. PubMed ID: 5122078 [No Abstract] [Full Text] [Related]
26. X-linked inheritance of ocular albinism with late-onset sensorineural deafness. Winship I; Gericke G; Beighton P Am J Med Genet; 1984 Dec; 19(4):797-803. PubMed ID: 6542750 [TBL] [Abstract][Full Text] [Related]
27. [Albinism. Current clinical and molecular genetic aspects of an important differential congenital nystagmus diagnosis]. Lorenz B Ophthalmologe; 1997 Jul; 94(7):534-44. PubMed ID: 9333404 [No Abstract] [Full Text] [Related]
28. [A new case of Waardenburg's syndrome]. Malbrel C; Longuebray P; Jouhaud F Bull Soc Ophtalmol Fr; 1982 Apr; 82(4):579-81. PubMed ID: 7105357 [No Abstract] [Full Text] [Related]
29. [Inborn defectx of lipid metabolism. 23. Coincidence of type 3 hyperlipoproteinemia and albinism]. Sobra J; Jílek M Cas Lek Cesk; 1971 May; 110(19):451-3. PubMed ID: 5574744 [No Abstract] [Full Text] [Related]
30. Autosomal dominant cone-rod dystrophy: a linkage study with 17 biochemical and serological markers. Ferrell RE; Hittner HM; Chakravarti A Am J Med Genet; 1981; 8(3):363-9. PubMed ID: 6940444 [TBL] [Abstract][Full Text] [Related]
31. [Hereditary optic atrophies. Study of a family with dominant autosomal optic atrophy]. Sebastián de Erice M; Romero López J; Navarro Esteban J; Jiménez F; Soto Faure L Rev Clin Esp; 1981 Dec; 163(5):341-3. PubMed ID: 7342192 [No Abstract] [Full Text] [Related]
32. Oculocutaneous albinism, immunodeficiency, hematological disorders, and minor anomalies: a new autosomal recessive syndrome? Kotzot D; Richter K; Gierth-Fiebig K Am J Med Genet; 1994 Apr; 50(3):224-7. PubMed ID: 8042664 [TBL] [Abstract][Full Text] [Related]
38. [Albinism and congenital mesodermal dysplasia of the cornea. Clinical and genetic study]. Valvo A; Romei L; Morin J Minerva Oftalmol; 1968; 10(6):268-72. PubMed ID: 5736378 [No Abstract] [Full Text] [Related]
39. Hereditary puzzles in albinism: heterogeneity or phenotypical variation? Taylor WO Trans Ophthalmol Soc U K (1962); 1983; 103 ( Pt 3)():318-30. PubMed ID: 6585074 [TBL] [Abstract][Full Text] [Related]
40. Birth prevalence and mutation spectrum in danish patients with autosomal recessive albinism. Grønskov K; Ek J; Sand A; Scheller R; Bygum A; Brixen K; Brondum-Nielsen K; Rosenberg T Invest Ophthalmol Vis Sci; 2009 Mar; 50(3):1058-64. PubMed ID: 19060277 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]