These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
155 related articles for article (PubMed ID: 2896232)
1. Prenatal diagnosis and carrier detection of genetic diseases by analysis of deoxyribonucleic acid. Ostrer H; Hejtmancik JF J Pediatr; 1988 May; 112(5):679-87. PubMed ID: 2896232 [No Abstract] [Full Text] [Related]
2. Prenatal diagnosis of Duchenne muscular dystrophy by DNA analysis. Old JM; Davies KE J Med Genet; 1986 Dec; 23(6):556-9. PubMed ID: 2879927 [TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis and carrier detection by DNA analysis. Cutting GR; Antonarakis SE Pediatr Rev; 1992 Apr; 13(4):138-43. PubMed ID: 1626008 [No Abstract] [Full Text] [Related]
4. [Use of DNA polymorphism in the diagnosis of human genetic diseases]. Cebrat S Postepy Hig Med Dosw; 1988; 42(5):461-82. PubMed ID: 2908211 [No Abstract] [Full Text] [Related]
5. Obstetricians should get ready for expanded carrier screening. Lau TK BJOG; 2016 Sep; 123 Suppl 3():36-8. PubMed ID: 27627595 [No Abstract] [Full Text] [Related]
6. Applications and limitations of direct DNA analysis in genetic prediction. Pembrey ME J Inherit Metab Dis; 1986; 9 Suppl 1():38-48. PubMed ID: 2878114 [TBL] [Abstract][Full Text] [Related]
7. Rapid detection and prenatal diagnosis of beta-thalassaemia: studies in Indian and Cypriot populations in the UK. Old JM; Varawalla NY; Weatherall DJ Lancet; 1990 Oct; 336(8719):834-7. PubMed ID: 1976877 [TBL] [Abstract][Full Text] [Related]
8. Haemophilia A: carrier detection and prenatal diagnosis by linkage analysis using DNA polymorphism. Tuddenham EG; Goldman E; McGraw A; Kernoff PB J Clin Pathol; 1987 Sep; 40(9):971-7. PubMed ID: 2889753 [TBL] [Abstract][Full Text] [Related]
9. DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure. Bakker E; Bonten EJ; De Lange LF; Veenema H; Majoor-Krakauer D; Hofker MH; Van Ommen GJ; Pearson PL J Med Genet; 1986 Dec; 23(6):573-80. PubMed ID: 2879929 [TBL] [Abstract][Full Text] [Related]
10. Amplification refractory mutation system for prenatal diagnosis and carrier assessment in cystic fibrosis. Newton CR; Heptinstall LE; Summers C; Super M; Schwarz M; Anwar R; Graham A; Smith JC; Markham AF Lancet; 1989 Dec 23-30; 2(8678-8679):1481-3. PubMed ID: 2574768 [TBL] [Abstract][Full Text] [Related]
13. DNA in medicine. Human genetics. White RL Lancet; 1984 Dec; 2(8414):1257-62. PubMed ID: 6150287 [No Abstract] [Full Text] [Related]
14. Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy by restriction fragment length polymorphism analysis with pERT 87 deoxyribonucleic acid probes. Katayama S; Montano M; Slotnick RN; Lebo RV; Golbus MS Am J Obstet Gynecol; 1988 Mar; 158(3 Pt 1):548-55. PubMed ID: 2894769 [TBL] [Abstract][Full Text] [Related]
15. Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms. Lindlöf M; Kääriäinen H; Davies KE; de la Chapelle A J Med Genet; 1986 Dec; 23(6):560-72. PubMed ID: 2879928 [TBL] [Abstract][Full Text] [Related]
16. Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophy. Meredith AL; Huson SM; Lunt PW; Sarfarazi M; Harley HG; Brook JD; Shaw DJ; Harper PS Br Med J (Clin Res Ed); 1986 Nov; 293(6558):1353-6. PubMed ID: 2878705 [TBL] [Abstract][Full Text] [Related]
17. DNA techniques in prenatal diagnosis and in genetic pathology. Rehder H; Friedrich U Am J Med Genet Suppl; 1987; 3():1-14. PubMed ID: 2897201 [TBL] [Abstract][Full Text] [Related]
18. Demonstration of a recent mutation in a family with isolated hemophilia A. Rudzki Z; Rodgers SE; Casey G; Mulley JC; Sutherland GR; Lloyd JV Aust N Z J Med; 1987 Dec; 17(6):609-10. PubMed ID: 2895997 [No Abstract] [Full Text] [Related]
19. The clinical applications of DNA polymorphisms. Thein SL; Wainscoat JS Dis Markers; 1986 Oct; 4(3):203-18. PubMed ID: 2898316 [No Abstract] [Full Text] [Related]
20. Ethnicity-Based Carrier Screening. King JR; Klugman S Obstet Gynecol Clin North Am; 2018 Mar; 45(1):83-101. PubMed ID: 29428288 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]