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22. [GENETIC HETEROGENITY IN HUMAN ACATALASIA]. HAMILTON HB; NEEL JV Jinrui Idengaku Zasshi; 1964 Mar; 9():46-56. PubMed ID: 14236257 [No Abstract] [Full Text] [Related]
23. [GOITROUS HYPOTHYROIDISM CAUSED BY A DEFECT IN THE IODINE "ORGANIFICATION" PROCESS. A CASE REPORT ON TWINS]. PENA J; BELMONTE AV; TOJO R Rev Esp Pediatr; 1965; 21():103-22. PubMed ID: 14343662 [No Abstract] [Full Text] [Related]
24. The application of genetics in medicine today. Goodman RM Ohio State Med J; 1966 Jan; 62(1):33-9. PubMed ID: 5998557 [No Abstract] [Full Text] [Related]
25. [On the diagnosis and therapy of hereditary protein defects especially hemophilias and the antibody deficiency syndrome]. Oehme J Kinderarztl Prax; 1965 Sep; 33(9):409-22. PubMed ID: 5866502 [No Abstract] [Full Text] [Related]
26. [Importance and possibilities of human genetics in modern medicine]. Kolbas V Med Glas; 1965 Oct; 19(10):272-7. PubMed ID: 5871304 [No Abstract] [Full Text] [Related]
28. [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]
29. Some clinical problems encountered in medical genetics. Slate WG Del Med J; 1973 Aug; 45(8):225-30. PubMed ID: 4728205 [No Abstract] [Full Text] [Related]
30. [ON CONGENITAL METABOLIC DISORDERS AND THEIR INCIDENCE]. ARIMA M Sogo Rinsho; 1963 Dec; 12():2256-62. PubMed ID: 14101458 [No Abstract] [Full Text] [Related]
31. [GONADAL DYSGENESIS (TURNER'S SYNDROME): A RARE DISEASE BUT VALUABLE INSTRUCTIVELY; A CHROMOSOME STUDY OF 35 CASES]. ENGEL E Schweiz Med Wochenschr; 1964 Jun; 94():906-14. PubMed ID: 14238349 [No Abstract] [Full Text] [Related]
32. [Inborn errors of metabolism at the molecular level]. Nakajima H Tanpakushitsu Kakusan Koso; 1968 Apr; 13(4):298-310. PubMed ID: 4881539 [No Abstract] [Full Text] [Related]
33. Inborn errors of metabolism: some thoughts about their basic mechanisms. Howell RR Pediatrics; 1970 Jun; 45(6):901-5. PubMed ID: 4912255 [No Abstract] [Full Text] [Related]
34. ENZYMES AND DRUG SENSITIVITY. THE GENETICS OF SERUM CHOLINESTERASE 'DEFICIENCY' IN RELATION TO SUXAMETHONIUM APNOEA. HARRIS H Proc R Soc Med; 1964 Jun; 57(6):503-6. PubMed ID: 14190871 [No Abstract] [Full Text] [Related]
35. [Inborn errors of metabolism and their implications for medicine]. Velázquez A Gac Med Mex; 1980 Nov; 116(11):503-14. PubMed ID: 7009299 [No Abstract] [Full Text] [Related]
36. Genetics and the physician. Delva PL N S Med Bull; 1965 Dec; 44(12):299-300. PubMed ID: 5215355 [No Abstract] [Full Text] [Related]
37. [Genetics and nutrition]. Gedda L; Milani-Comparetti M Munch Med Wochenschr; 1971 Mar; 113(13):453-8. PubMed ID: 5107949 [No Abstract] [Full Text] [Related]
38. GENETIC MECHANISMS PRODUCING MULTIPLE ENZYME DEFECTS. A REVIEW OF UNEXPLAINED CASES AND A NEW HYPOTHESIS. AUERBACH VH; DIGEORGE AM Am J Med Sci; 1965 Jun; 249():718-47. PubMed ID: 14301353 [No Abstract] [Full Text] [Related]
39. [FOUR CASES OF THYROTOXIC MYOPATHY]. TOKUOMI H; OKAJIMA T; TAKABA M; MATSUI S; YAMASHITA M; HATA K; OKADA T No To Shinkei; 1963 Oct; 15():955-60. PubMed ID: 14052954 [No Abstract] [Full Text] [Related]