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26. [The genetic polymorphism of haptoglobin and the severity of essential arterial hypertension]. Monteiro CP; Lança H; Joaquim N; Lamy I; Aníbal J; Coucelo J; Coucelo JA; Azevedo J; Bicho MP Rev Port Cardiol; 1997 Jan; 16(1):81-4. PubMed ID: 9115782 [No Abstract] [Full Text] [Related]
27. An informative large pedigree with four compound hemizygotes of three combinations of deutan and protan genes. Arias S; Rodríguez A Acta Cient Venez; 1973; 24(2):44-52. PubMed ID: 4549004 [No Abstract] [Full Text] [Related]
28. Absence of genetic linkage between polymorphisms of the insulin receptor gene and essential hypertension. Munroe PB; Daniel HI; Farrall M; Lawson M; Bouloux PM; Caulfield MJ J Hum Hypertens; 1995 Aug; 9(8):669-70. PubMed ID: 8523386 [TBL] [Abstract][Full Text] [Related]
29. Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxia. Worth PF; Houlden H; Giunti P; Davis MB; Wood NW Nat Genet; 2000 Mar; 24(3):214-5. PubMed ID: 10700168 [No Abstract] [Full Text] [Related]
31. Spastic paraplegia, epilepsy, and mental retardation in several members of a family: a novel genetic disorder. Gigli GL; Diomedi M; Bernardi G; Placidi F; Marciani MG; Calia E; Maschio MC; Neri G Am J Med Genet; 1993 Mar; 45(6):711-6. PubMed ID: 8456849 [TBL] [Abstract][Full Text] [Related]
32. Segregation analysis comparing liability and quantitative trait models for hypertension using the Genetic Analysis Workshop 13 simulated data. Crockford GP; Bishop DT; Barrett JH BMC Genet; 2003 Dec; 4 Suppl 1(Suppl 1):S79. PubMed ID: 14975147 [TBL] [Abstract][Full Text] [Related]
33. [Role of genealogical study in evaluating the factor of ah hereditary predisposition to hypertension]. Madoian SKh Zh Eksp Klin Med; 1978; 18(3):103-7. PubMed ID: 150772 [No Abstract] [Full Text] [Related]
34. [Albinism in certain clinical and genetic arieties. Study and research on a family]. Morra M Minerva Oftalmol; 1967; 9(6):202-5. PubMed ID: 5617749 [No Abstract] [Full Text] [Related]
37. [Hypo-/aplasia of the nasal bones--an autosomal dominant inherited anomaly]. Ernst M; Schilbach U HNO; 1987 Nov; 35(11):478-81. PubMed ID: 3692934 [TBL] [Abstract][Full Text] [Related]
38. [Autosomal dominant transmission of familial idiopathic hypoparathyroidism]. Proto G; Barberi M; Cattalini M; Bertolissi F Minerva Endocrinol; 1985; 10(4):217-22. PubMed ID: 3834313 [No Abstract] [Full Text] [Related]