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33. [Early detection of inborn errors of metabolism (author's transl)]. Kitagawa T Rinsho Byori; 1976; 24(6):490-6. PubMed ID: 988267 [No Abstract] [Full Text] [Related]
34. Amniocentesis in the prenatal diagnosis of genetic disorders and congenital defects. Padilla LM J Indiana State Med Assoc; 1983 Oct; 76(10):669-75. PubMed ID: 6644072 [No Abstract] [Full Text] [Related]
35. Screening, counselling and treatment of hereditary metabolic disease; a survey of resources in Canada. Haworth JC; Miller JR; Scriver CR Can Med Assoc J; 1974 Nov; 111(10):1147-50, 1153. PubMed ID: 4429943 [No Abstract] [Full Text] [Related]
36. [Perspectives in medical genetics]. Saldanha PH Rev Hosp Clin Fac Med Sao Paulo; 1978 Apr; 33(2):114-20. PubMed ID: 663515 [No Abstract] [Full Text] [Related]
37. Basic concepts in biochemical antenatal diagnosis. Grebner EE Obstet Gynecol Clin North Am; 1993 Sep; 20(3):421-31. PubMed ID: 8278142 [TBL] [Abstract][Full Text] [Related]
38. [Prenatal diagnosis: a new problem]. Cutillo S Pediatria (Napoli); 1980 Jun; 88(2):V-VII. PubMed ID: 7243515 [No Abstract] [Full Text] [Related]
39. [Diagnosis and acute treatment of inborn metabolic diseases in infants]. Lund AM; Christensen E; Skovby F Ugeskr Laeger; 2002 Nov; 164(48):5613-9. PubMed ID: 12523004 [TBL] [Abstract][Full Text] [Related]
40. [Prenatal diagnosis of hereditary enzymopathies]. Tsvetkova IV Vestn Akad Med Nauk SSSR; 1984; (8):70-4. PubMed ID: 6495831 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]