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2. [Human genetics in hematological disorders]. Fujiki N; Shibuya Y; Saito T; Takebayashi M; Mibayashi E Saishin Igaku; 1967 Dec; 22(12):2676-85. PubMed ID: 4874574 [No Abstract] [Full Text] [Related]
3. Genetic diseases among Jews. Adam A Isr J Med Sci; 1973; 9(9):1383-92. PubMed ID: 4590458 [No Abstract] [Full Text] [Related]
4. The application of bacterial genetics to the study of human genetic abnormalities. Dreyfus JC Prog Med Genet; 1969; 6():169-200. PubMed ID: 4897152 [No Abstract] [Full Text] [Related]
7. [The prevention of hereditary erythrocytic diseases]. Lamy S; Braga L; Pacheco P; Lavinha J; da Costa GG; Ferreira NC Acta Med Port; 1995 Jun; 8(6):355-8. PubMed ID: 7653290 [TBL] [Abstract][Full Text] [Related]
8. [Diseases in children--genetic mutation]. Osowiecki H Pieleg Polozna; 1975 Mar; (3):3-5. PubMed ID: 1038754 [No Abstract] [Full Text] [Related]
9. [Sex difference in inborn errors of metabolism and epilepsy]. Kodama H; Kamoshita S No To Shinkei; 1983 Sep; 35(9):877-85. PubMed ID: 6651986 [No Abstract] [Full Text] [Related]
10. Hematological abnormalities in inborn errors of metabolism--how frequent are they? The Cretan experience. Evangeliou A; Dafnis E; Perdikoyanni C; Spilioti M; Lionis C; Kalmanti M Pediatr Hematol Oncol; 2002 Dec; 19(8):581-5. PubMed ID: 12487834 [TBL] [Abstract][Full Text] [Related]
11. [Familial Mediterranean Fever (FMF): from diagnosis to treatment]. Medlej-Hashim M; Loiselet J; Lefranc G; Mégarbané A Sante; 2004; 14(4):261-6. PubMed ID: 15745878 [TBL] [Abstract][Full Text] [Related]
12. [The incidence of porphyria in Finland]. Mustajoki P; Koskelo P Duodecim; 1974; 90(17):1157-66. PubMed ID: 4411165 [No Abstract] [Full Text] [Related]
14. [Genogeography of hereditary metabolic diseases in the USSR]. Krasnopol'skaia KD Vestn Akad Med Nauk SSSR; 1984; (7):38-44. PubMed ID: 6382856 [No Abstract] [Full Text] [Related]
15. [Internal medicine and pediatrics, with reference to genetic counseling]. Fujiki N; Takenaka S; Ishimaru T; Sugimoto N; Sasaki T Saishin Igaku; 1966 Jul; 21(7):1549-56. PubMed ID: 5338595 [No Abstract] [Full Text] [Related]
16. [The genetic code in metabolic hereditary diseases]. Cozza A Ann Med Nav (Roma); 1968; 73(3):239-41. PubMed ID: 5736469 [No Abstract] [Full Text] [Related]
17. [Acute intermittent porphyria in Saltdal]. Eldøen O; Sandvik A Tidsskr Nor Laegeforen; 1982 Jun; 102(16):902-6. PubMed ID: 7164041 [No Abstract] [Full Text] [Related]
18. [Mutation diagnosis is a possibility for the half of the families with acute intermittent porphyria]. Anvret M; Lee JS; Lundin G Lakartidningen; 1991 Jul; 88(30-31):2513-4. PubMed ID: 1865718 [No Abstract] [Full Text] [Related]