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2. Application of endonuclease mapping to the analysis and prenatal diagnosis of thalassemias caused by globin-gene deletion. Orkin SH; Alter BP; Altay C; Mahoney MJ; Lazarus H; Hobbins JC; Nathan DG N Engl J Med; 1978 Jul; 299(4):166-72. PubMed ID: 661890 [TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis of homozygous alpha thalassaemia by direct DNA analysis of uncultured amniotic fluid cells. Chan V; Ghosh A; Chan TK; Wong V; Todd D Br Med J (Clin Res Ed); 1984 May; 288(6427):1327-9. PubMed ID: 6324946 [TBL] [Abstract][Full Text] [Related]
5. Diagnosis of homozygous alpha-thalassemia in cultured amniotic-fluid fibroblasts. Wong V; Ma HK; Todd D; Golbus MS; Dozy AM; Kan YW N Engl J Med; 1978 Mar; 298(12):669-70. PubMed ID: 628389 [No Abstract] [Full Text] [Related]
6. Successful application of prenatal diagnosis in a pregnancy at risk for homozygous beta-thalassemia. Kan YW; Golbus MS; Klein P; Dozy AM N Engl J Med; 1975 May; 292(21):1096-9. PubMed ID: 1128553 [TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of alpha-thalassemia. Clinical application of molecular hybridization. Kan YW; Golbus MS; Dozy AM N Engl J Med; 1976 Nov; 295(21):1165-7. PubMed ID: 980019 [TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of thalassemias and hemoglobinopathies. Seale TW; Rennert OM Ann Clin Lab Sci; 1980; 10(5):383-94. PubMed ID: 6252819 [TBL] [Abstract][Full Text] [Related]
9. Accurate prenatal diagnosis of Hb Bart's hydrops fetalis in daily practice with a double-check PCR system. Karnpean R; Fucharoen G; Fucharoen S; Sae-ung N; Sanchaisuriya K; Ratanasiri T Acta Haematol; 2009; 121(4):227-33. PubMed ID: 19546525 [TBL] [Abstract][Full Text] [Related]
10. Alpha-globin gene organisation and prenatal diagnosis of alpha-thalassaemia in Chinese. Zeng YT; Huang SZ Lancet; 1985 Feb; 1(8424):304-7. PubMed ID: 2857363 [TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of hemoglobin H disease. Koenig HM; Vedvick TS; Dozy AM; Golbus MS; Kan YW J Pediatr; 1978 Feb; 92(2):278-81. PubMed ID: 74407 [TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis of alpha- and beta-thalassaemias in Singapore--current status. Tan JA; Tay SH; Siang OK; Lai PS; Boon WH; Kham S Ann Trop Paediatr; 1991; 11(1):67-74. PubMed ID: 1714698 [TBL] [Abstract][Full Text] [Related]
13. New clinical implications of molecular genetics. Kurnit DM; Motulsky AG JAMA; 1979 Apr; 241(15):1616-8. PubMed ID: 85727 [No Abstract] [Full Text] [Related]
15. Prenatal diagnosis by DNA analysis. Kan YW; Chang JC; Dozy AM Birth Defects Orig Artic Ser; 1982; 18(7):275-83. PubMed ID: 6297633 [No Abstract] [Full Text] [Related]
16. Polymorphism of DNA sequence in the beta-globin gene region. Application to prenatal diagnosis of beta 0 thalassemia in Sardinia. Kan YW; Lee KY; Furbetta M; Angius A; Cao A N Engl J Med; 1980 Jan; 302(4):185-8. PubMed ID: 6927915 [TBL] [Abstract][Full Text] [Related]
17. Alpha-thalassemia incidence in southern Thailand by restriction endonuclease analysis of globin DNA from placental blood at Songklanagarind Hospital. Sriroongrueng W; Pornpatkul M; Panich V; Fucharoen S Southeast Asian J Trop Med Public Health; 1997; 28 Suppl 3():93-6. PubMed ID: 9640606 [TBL] [Abstract][Full Text] [Related]
18. Alpha-thalassemia: prenatal diagnosis and neonatal implications. Maberry MC; Klein VR; Boehm C; Warren TC; Gilstrap LC Am J Perinatol; 1990 Oct; 7(4):356-8. PubMed ID: 2222628 [TBL] [Abstract][Full Text] [Related]
19. Model for antenatal diagnosis of beta-thalassaemia and other monogenic disorders by molecular analysis of linked DNA polymorphisms. Little PF; Annison G; Darling S; Williamson R; Camba L; Modell B Nature; 1980 May; 285(5761):144-7. PubMed ID: 6246441 [TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of beta-thalassemia. Detection of a single nucleotide mutation in DNA. Pirastu M; Kan YW; Cao A; Conner BJ; Teplitz RL; Wallace RB N Engl J Med; 1983 Aug; 309(5):284-7. PubMed ID: 6866053 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]