143 related articles for article (PubMed ID: 21107727)
1. An artifact band frequently associated with variable number of tandem repeat marker at phenylalanine hydroxylase gene: application in carrier detection and prenatal diagnosis of phenylketonuria.
Fazeli Z; Vallian S
Mol Biol Rep; 2011 Jun; 38(5):3395-9. PubMed ID: 21107727
[TBL] [Abstract][Full Text] [Related]
2. [Analysis of short tandem repeats polymorphism in the phenylalanine hydroxylase gene and its application to prenatal gene diagnosis of phenylketonuria].
Huang S; Fang B; Chu H
Zhonghua Yi Xue Za Zhi; 1995 Jan; 75(1):22-4, 61. PubMed ID: 7600314
[TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis by minisatellite analysis in Italian families with phenylketonuria.
Romano V; Dianzani I; Ponzone A; Zammarchi E; Eisensmith R; Ceratto N; Bosco P; Indelicato A
Prenat Diagn; 1994 Oct; 14(10):959-62. PubMed ID: 7899270
[TBL] [Abstract][Full Text] [Related]
4. Carrier detection of phenylketonuria in Iranian families by variable number tandem-repeat polymorphism analysis.
Hosseini-Mazinani SM; Koochmeshgi J; Khazaee-Koohpar Z; Hosein-Pur-Nobari N; Seifati SM
East Mediterr Health J; 2008; 14(6):1445-51. PubMed ID: 19161120
[TBL] [Abstract][Full Text] [Related]
5. Polymorphic DNA haplotypes at the phenylalanine hydroxylase locus in prenatal diagnosis of phenylketonuria.
Daiger SP; Lidsky AS; Chakraborty R; Koch R; Güttler F; Woo SL
Lancet; 1986 Feb; 1(8475):229-32. PubMed ID: 2868252
[TBL] [Abstract][Full Text] [Related]
6. Extensive restriction site polymorphism at the human phenylalanine hydroxylase locus and application in prenatal diagnosis of phenylketonuria.
Lidsky AS; Ledley FD; DiLella AG; Kwok SC; Daiger SP; Robson KJ; Woo SL
Am J Hum Genet; 1985 Jul; 37(4):619-34. PubMed ID: 9556654
[TBL] [Abstract][Full Text] [Related]
7. Detection of point mutations of the phenylalanine hydroxylase gene and prenatal diagnosis of phenylketonuria.
Fang B; Yuan L; Wang M; Huang S; Wang T; Miao S; Ye J; Sun N; Lo H; Savio LC
Chin Med Sci J; 1992 Dec; 7(4):205-8. PubMed ID: 1307495
[TBL] [Abstract][Full Text] [Related]
8. A single polymorphic STR system in the human phenylalanine hydroxylase gene permits rapid prenatal diagnosis and carrier screening for phenylketonuria.
Goltsov AA; Eisensmith RC; Naughton ER; Jin L; Chakraborty R; Woo SL
Hum Mol Genet; 1993 May; 2(5):577-81. PubMed ID: 8100164
[TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis and carrier detection of classic phenylketonuria by gene analysis.
Woo SL
Pediatrics; 1984 Sep; 74(3):412-23. PubMed ID: 6472974
[No Abstract] [Full Text] [Related]
10. A simple, rapid, and highly informative PCR-based procedure for prenatal diagnosis and carrier screening of phenylketonuria.
Eisensmith RC; Goltsov AA; Woo SL
Prenat Diagn; 1994 Dec; 14(12):1113-8. PubMed ID: 7899279
[TBL] [Abstract][Full Text] [Related]
11. Rapid carrier screening using short tandem repeats in the phenylalanine hydroxylase gene.
Shawky RM; el-Aleem KA; Rifaat MM; el-Naggar RL; Marzouk GM
East Mediterr Health J; 2002 Jan; 8(1):49-54. PubMed ID: 15330560
[TBL] [Abstract][Full Text] [Related]
12. RFLPs of the phenylalanine hydroxylase gene in the Italian population.
Dianzani I; Farinasso L; Fortina P; Camaschella C; Ponzone R; Dahl HH; Cotton RG; Ponzone A
J Inherit Metab Dis; 1989; 12(2):162-5. PubMed ID: 2569049
[TBL] [Abstract][Full Text] [Related]
13. [The power of linkage analysis on PAH gene in prenatal gene diagnosis is improved with three additional short tandem repeat markers].
Yao FX; Guo H; Han JJ; Meng Y; Sun NH; Huang SZ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):382-6. PubMed ID: 17680525
[TBL] [Abstract][Full Text] [Related]
14. [Frequencies of 6 known mutations in phenylalanine hydroxylase gene and their application in prenatal gene diagnosis].
Wang M
Zhonghua Yi Xue Za Zhi; 1992 Nov; 72(11):670-3, 702-3. PubMed ID: 1338705
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis of phenylketonuria.
Kohli S; Saxena R; Thomas E; Rao P; Verma IC
Indian J Med Res; 2005 Nov; 122(5):400-3. PubMed ID: 16456253
[TBL] [Abstract][Full Text] [Related]
16. [Spectrum of phenylalanine hydroxylase gene mutations and genotype-phenotype correlation in the patients with phenylketonuria in Beijing area of China].
Qu YJ; Song F; Jin YW; Wang H; Zhang YM; Qin JL; Qiu L
Zhonghua Er Ke Za Zhi; 2008 Feb; 46(2):115-9. PubMed ID: 19099685
[TBL] [Abstract][Full Text] [Related]
17. Molecular studies and prenatal diagnosis of phenylketonuria in Chinese patients.
Fan GX; Qing LX; Jun Y; Mei Z
Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():63-5. PubMed ID: 11400788
[TBL] [Abstract][Full Text] [Related]
18. Molecular Genetic Analysis of the Variable Number of Tandem-Repeat Alleles at the Phenylalanine Hydroxylase Gene in Iranian Azeri Turkish Population.
Bagheri M; Abdi Rad I; Hosseini Jazani N; Zarrin R; Ghazavi A
Iran Biomed J; 2015; 19(3):183-7. PubMed ID: 26025954
[TBL] [Abstract][Full Text] [Related]
19. [Application of capillary non-gel sieving electrophoresis to the analysis of short tandem repeat in phenylalanine hydroxylase gene and gene diagnosis of phenylketonuria].
Xu Q; Song F; Han F; Lin B; Shen Y
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1998 Dec; 20(6):433-9. PubMed ID: 11717935
[TBL] [Abstract][Full Text] [Related]
20. Mutation Analysis in Classical Phenylketonuria Patients Followed by Detecting Haplotypes Linked to Some PAH Mutations.
Dehghanian F; Silawi M; Tabei SM
Clin Lab; 2017 Feb; 63(2):295-300. PubMed ID: 28182360
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
