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32. A pedigree of binocular heterochromia iridis associated with other anomalies (Waardenburg-Klein syndrome). Basile R J Genet Hum; 1965 Sep; 14(2):87-91. PubMed ID: 5849255 [No Abstract] [Full Text] [Related]
33. [Primary hepatic overload of the brown pigment type. The problem of lipofuscins]. Lageron A; Paraf A; Trad J; Desche S Rev Med Chir Mal Foie; 1968 Apr; 43(2):55-72. PubMed ID: 5688553 [No Abstract] [Full Text] [Related]
34. Genetic heterogeneity in the Waardenburg syndrome. Arias S Birth Defects Orig Artic Ser; 1971 Mar; 07(4):87-101. PubMed ID: 5006208 [TBL] [Abstract][Full Text] [Related]
35. [Bronze baby syndrome (unusual complication of phototherapy)]. Márk Z; Balázs M; Bíró E; Lukács VF Orv Hetil; 1981 Mar; 122(11):641-3. PubMed ID: 7254797 [No Abstract] [Full Text] [Related]
36. [Congenital diseases of bilirubin metabolism]. Sinaasappel M Tijdschr Kindergeneeskd; 1993 Aug; 61(4):135-40. PubMed ID: 8122224 [TBL] [Abstract][Full Text] [Related]
38. Syndromic albinism: a review of genetics and phenotypes. Scheinfeld NS Dermatol Online J; 2003 Dec; 9(5):5. PubMed ID: 14996378 [TBL] [Abstract][Full Text] [Related]
39. [A Swiss family with Klein-Waardenburg's syndrome associated with hyperkeratosis of the palms and feet and with serious oligophrenia]. Amini-Elihou S J Genet Hum; 1970 Dec; 18(4):307-63. PubMed ID: 5524816 [No Abstract] [Full Text] [Related]
40. Ocular findings in Chediak-Higashi disease: a light and electron microscopic study of two patients. Libert J; Dhermy P; Van Hoof F; Dufier JL; Cornu G Birth Defects Orig Artic Ser; 1982; 18(6):327-44. PubMed ID: 7171764 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]