105 related articles for article (PubMed ID: 8710781)
1. Prenatal diagnosis of adrenoleukodystrophy by means of mutation analysis.
Imamura A; Suzuki Y; Song XQ; Fukao T; Shimozawa N; Orii T; Kondo N
Prenat Diagn; 1996 Mar; 16(3):259-61. PubMed ID: 8710781
[TBL] [Abstract][Full Text] [Related]
2. DNA-based diagnostics for adrenoleukodystrophy in a large New Zealand family.
Rowland SA; Dodd A; Roche AL; Manilal S; Kennedy MA; Becroft DM; Tonkin S; Chapman C; Love DR
N Z Med J; 1996 Aug; 109(1028):312-5. PubMed ID: 8816721
[TBL] [Abstract][Full Text] [Related]
3. A point mutation at ATP-binding region of the ALD gene in a family with X-linked adrenoleukodystrophy.
Matsumoto T; Kondoh T; Masuzaki H; Harada N; Matsusaka T; Kinoshita E; Takeo G; Tsujihata M; Suzuki Y; Tsuji Y
Jpn J Hum Genet; 1994 Sep; 39(3):345-51. PubMed ID: 7841445
[TBL] [Abstract][Full Text] [Related]
4. Prenatal diagnosis of X-linked adrenoleukodystrophy combining biochemical, immunocytochemical and DNA analyses.
Maier EM; Roscher AA; Kammerer S; Mehnert K; Conzelmann E; Holzinger A
Prenat Diagn; 1999 Apr; 19(4):364-8. PubMed ID: 10327143
[TBL] [Abstract][Full Text] [Related]
5. Prenatal diagnosis in a Chinese family with type Ia glycogen storage disease by PCR-based genetic analysis.
Lee WJ; Yang CH; Ho ES; Shih A; Lin LY; Lin WH
Prenat Diagn; 1996 Nov; 16(11):1027-31. PubMed ID: 8953636
[TBL] [Abstract][Full Text] [Related]
6. X-linked adrenoleukodystrophy (ALD): a novel mutation of the ALD gene in 6 members of a family presenting with 5 different phenotypes.
Berger J; Molzer B; Faé I; Bernheimer H
Biochem Biophys Res Commun; 1994 Dec; 205(3):1638-43. PubMed ID: 7811247
[TBL] [Abstract][Full Text] [Related]
7. [Prenatal molecular diagnosis of four fetuses at high risk for X-linked adrenoleukodystrophy].
Ke LF; Wang ZH; Huang HJ; Tu XD; Zeng J; Li B; Yang BS; Lan FH
Zhonghua Fu Chan Ke Za Zhi; 2008 Jan; 43(1):25-8. PubMed ID: 18366928
[TBL] [Abstract][Full Text] [Related]
8. Prenatal molecular diagnosis of adrenoleukodystrophy.
Huang LH; Huang HJ; Yang BS; Tu XD; Zeng J; Li HZ; Xin N; Lan FH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Dec; 22(6):612-5. PubMed ID: 16331554
[TBL] [Abstract][Full Text] [Related]
9. Preimplantation genetic diagnosis of X-linked adrenoleukodystrophy with gender determination using multiple displacement amplification.
Lledó B; Bernabeu R; Ten J; Galán FM; Cioffi L
Fertil Steril; 2007 Nov; 88(5):1327-33. PubMed ID: 17498713
[TBL] [Abstract][Full Text] [Related]
10. Attitudes toward presymptomatic testing and prenatal diagnosis for adrenoleukodystrophy among affected families.
Costakos D; Abramson RK; Edwards JG; Rizzo WB; Best RG
Am J Med Genet; 1991 Dec; 41(3):295-300. PubMed ID: 1789282
[TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of beta-thalassemia in Egypt: implementing accurate high-tech methods did not reflect much on the outcome.
Elgawhary S; Elbaradie Sahar MY; Rashad WM; Mosaad M; Abdalla MA; Ezzat G; Wali YA; Elbeshlawy A
Pediatr Hematol Oncol; 2008 Sep; 25(6):541-8. PubMed ID: 18728973
[TBL] [Abstract][Full Text] [Related]
12. Molecular prenatal diagnosis of glycogen storage disease type Ia.
Qu Y; Abdenur JE; Eng CM; Desnick RJ
Prenat Diagn; 1996 Apr; 16(4):333-6. PubMed ID: 8734807
[TBL] [Abstract][Full Text] [Related]
13. Prenatal exclusion of Leigh syndrome due to T8993C mutation in the mitochondrial DNA.
Leshinsky-Silver E; Perach M; Basilevsky E; Hershkovitz E; Yanoov-Sharav M; Lerman-Sagie T; Lev D
Prenat Diagn; 2003 Jan; 23(1):31-3. PubMed ID: 12533809
[TBL] [Abstract][Full Text] [Related]
14. A rapid and sensitive protocol for prenatal molecular diagnosis of X-linked adrenoleukodystrophy.
Lan F; Wang Z; Ke L; Xie H; Huang L; Huang H; Tu X; Zheng D; Zeng J; Li H; Xin N; Yang B
Clin Chim Acta; 2010 Dec; 411(23-24):1992-7. PubMed ID: 20800589
[TBL] [Abstract][Full Text] [Related]
15. Mutation analysis of the ALD gene in seven Japanese families with X-linked adrenoleukodystrophy.
Matsumoto T; Tsuru A; Amamoto N; Shimizu T; Kondoh T; Saitoh N; Tsujii T; Tamagawa K
J Hum Genet; 2003; 48(3):125-9. PubMed ID: 12624723
[TBL] [Abstract][Full Text] [Related]
16. Genetic counselling and prenatal diagnosis of osteogenesis imperfecta caused by paternal mosaicism.
Lund AM; Schwartz M; Skovby F
Prenat Diagn; 1996 Nov; 16(11):1032-8. PubMed ID: 8953637
[TBL] [Abstract][Full Text] [Related]
17. Reliable co-segregation analysis for prenatal diagnosis and heterozygote detection in Gaucher disease.
Cormand B; Montfort M; Chabás A; Grinberg D; Vilageliu LL
Prenat Diagn; 1998 Mar; 18(3):207-12. PubMed ID: 9556036
[TBL] [Abstract][Full Text] [Related]
18. [Adrenomyeloneuropathy and adrenoleukodystrophy: genetic identity and detection. Apropos of a family].
Labauge P; Ducros A; Khalaf K; Pages M; Blard JM
Ann Med Interne (Paris); 1994; 145(1):53-5. PubMed ID: 8192283
[No Abstract] [Full Text] [Related]
19. First trimester prenatal diagnosis of adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysis to a DNA probe.
Boué J; Oberle I; Heilig R; Mandel JL; Moser A; Moser H; Larsen JW; Dumez Y; Boué A
Hum Genet; 1985; 69(3):272-4. PubMed ID: 3856557
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of congenital myotonic dystrophy and counseling of the pregnant mother: case report and literature review.
Geifman-Holtzman O; Fay K
Am J Med Genet; 1998 Jul; 78(3):250-3. PubMed ID: 9677060
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
