89 related articles for article (PubMed ID: 1359503)
1. [Molecular genetics and prenatal diagnosis].
Lyonnet S; Rozet JM; Martin C; Munnich A
Pediatrie; 1992; 47(5):359-63. PubMed ID: 1359503
[TBL] [Abstract][Full Text] [Related]
2. DNA-based prenatal diagnosis of heritable skin diseases.
Christiano AM; Uitto J
Arch Dermatol; 1993 Nov; 129(11):1455-9. PubMed ID: 7902070
[TBL] [Abstract][Full Text] [Related]
3. [First prenatal diagnosis of familial hypercholesterolemia by a molecular biology technic].
Stefanutti C; Vivenzio A
Clin Ter; 1993 Aug; 143(2):99-103. PubMed ID: 7900953
[TBL] [Abstract][Full Text] [Related]
4. [The prenatal diagnosis of hemophilia A--the use of PCR and family RFLP analysis].
Bian M
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1993 Apr; 15(2):102-7. PubMed ID: 7902217
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Basic principles of recombinant DNA use for prenatal diagnosis.
Goldberg JD
Semin Perinatol; 1990 Dec; 14(6):439-45. PubMed ID: 1981814
[No Abstract] [Full Text] [Related]
7. Prenatal diagnosis of inherited hemoglobinopathies.
Cao A; Pirastu M; Rosatelli C
Haematologica; 1990; 75 Suppl 5():169-77. PubMed ID: 1982278
[No Abstract] [Full Text] [Related]
8. Prenatal diagnosis of sickle cell anemia using PCR and restriction enzyme Dde I.
Gürgey A; Beksaç S; Mesci L; Cakar N; Karakaş U; Kutlar A; Altay C
Turk J Pediatr; 1993; 35(3):159-62. PubMed ID: 7909397
[TBL] [Abstract][Full Text] [Related]
9. Prenatal exclusion testing for Huntington disease using the polymerase chain reaction.
McIntosh I; Curtis A; Millan FA; Brock DJ
Am J Med Genet; 1989 Feb; 32(2):274-6. PubMed ID: 2564738
[TBL] [Abstract][Full Text] [Related]
10. Molecular diagnosis of Duchenne muscular dystrophy by use of a conformational polymorphism in the absence of DNA from an affected boy.
Tuffery S; Moine P; Sarda P; Lefort G; Boulot P; Demaille J; Claustres M
Genet Couns; 1994; 5(2):183-5. PubMed ID: 7917130
[TBL] [Abstract][Full Text] [Related]
11. [Recent advances in human molecular genetics].
Abe T
Rinsho Byori; 1990 Oct; 38(10):1093-100. PubMed ID: 1979824
[TBL] [Abstract][Full Text] [Related]
12. [Preliminary study on prenatal diagnosis from coelomic cells using polymerase chain reaction].
Sun LM; Wang DF; Liu JH
Zhonghua Fu Chan Ke Za Zhi; 2005 Dec; 40(12):812-4. PubMed ID: 16412325
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of cystic fibrosis in a highly heterogeneous population.
Casals T; Gimenez J; Ramos MD; Nunes V; Estivill X
Prenat Diagn; 1996 Mar; 16(3):215-22. PubMed ID: 8710774
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis in hemophilia A using factor VIII gene polymorphism--Indian experience.
Chowdhury MR; Tiwari M; Kabra M; Menon PS
Ann Hematol; 2003 Jul; 82(7):427-30. PubMed ID: 12768323
[TBL] [Abstract][Full Text] [Related]
15. Molecular analysis and prenatal prediction of spinal muscular atrophy in Chinese patients by the combination of restriction fragment length polymorphism analysis, denaturing high-performance liquid chromatography, and linkage analysis.
Chen WJ; Wu ZY; Lin MT; Su JF; Lin Y; Murong SX; Wang N
Arch Neurol; 2007 Feb; 64(2):225-31. PubMed ID: 17296838
[TBL] [Abstract][Full Text] [Related]
16. Genomic carrier detection and prenatal diagnosis of haemophilia A in families at risk using the polymerase chain reaction (PCR).
Wehnert M; Shukova EL; Surin VL; Schröder W; Solovjev GYa ; Grinjeva NI; Herrmann FH
Folia Haematol Int Mag Klin Morphol Blutforsch; 1990; 117(4):617-22. PubMed ID: 1714868
[TBL] [Abstract][Full Text] [Related]
17. Prenatal determinations of paternity by molecular genetic "fingerprinting".
Kovacs BW; Shahbahrami B; Medearis AL; Comings DE
Obstet Gynecol; 1990 Mar; 75(3 Pt 2):474-9. PubMed ID: 1968245
[TBL] [Abstract][Full Text] [Related]
18. [Early prenatal diagnosis using fetal cells acquired from different sites of uterine cervix: a preliminary study].
Zhang L; Duan T
Zhonghua Yi Xue Za Zhi; 2006 Sep; 86(33):2343-7. PubMed ID: 17156633
[TBL] [Abstract][Full Text] [Related]
19. [Prenatal screening for phenylketonuria in 2 families by trophoblast biopsy].
Rey F; Berthelon M; Munnich A; Frézal J; Rey J
Arch Fr Pediatr; 1987 Oct; 44(8):565-8. PubMed ID: 2894821
[TBL] [Abstract][Full Text] [Related]
20. DNA prenatal diagnosis.
Gilbert F; Marinduque B
Curr Opin Obstet Gynecol; 1990 Apr; 2(2):226-35. PubMed ID: 1983234
[No Abstract] [Full Text] [Related]
[Next] [New Search]
