311 related articles for article (PubMed ID: 19087561)
1. [Rapid genetic prenatal diagnosis for achondroplasia].
Zhu HY; Yang Y; Li J; Ru T; Hu YL
Zhonghua Fu Chan Ke Za Zhi; 2008 Nov; 43(11):810-3. PubMed ID: 19087561
[TBL] [Abstract][Full Text] [Related]
2. [Prenatal diagnosis of achondroplasia].
Huang X; Huang LH; Fang Q; Chen ML; Zhou Y; Cai J; Chen BJ; Chen JH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Aug; 25(4):427-9. PubMed ID: 18683143
[TBL] [Abstract][Full Text] [Related]
3. Improved prenatal detection of a fetal point mutation for achondroplasia by the use of size-fractionated circulatory DNA in maternal plasma--case report.
Li Y; Holzgreve W; Page-Christiaens GC; Gille JJ; Hahn S
Prenat Diagn; 2004 Nov; 24(11):896-8. PubMed ID: 15565648
[TBL] [Abstract][Full Text] [Related]
4. Detection of a de novo Y278C mutation in FGFR3 in a pregnancy with severe fetal hypochondroplasia: prenatal diagnosis and literature review.
Chen CP; Su YN; Lin TH; Chang TY; Su JW; Wang W
Taiwan J Obstet Gynecol; 2013 Dec; 52(4):580-5. PubMed ID: 24411048
[TBL] [Abstract][Full Text] [Related]
5. [Diagnosing achondroplasia by single cell nested-PCR].
Zhong CG; Li LY; Lu CF; Lin G; Fu JJ; Luo KL; Lu GX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Jun; 20(3):228-31. PubMed ID: 12778450
[TBL] [Abstract][Full Text] [Related]
6. Denaturing high-performance liquid chromatography (DHPLC)-based prenatal diagnosis for tuberous sclerosis.
Bénit P; Bonnefont JP; Kara Mostefa A; Francannet C; Munnich A; Ray PF
Prenat Diagn; 2001 Apr; 21(4):279-83. PubMed ID: 11288117
[TBL] [Abstract][Full Text] [Related]
7. An improved methodology for the detection of the common mutation in the FGFR3 gene responsible for achondroplasia.
Lanning RW; Brown CA
Hum Mutat; 1997; 10(6):496-9. PubMed ID: 9401015
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. Rapid genetic analysis of oculocutaneous albinism (OCA1) using denaturing high performance liquid chromatography (DHPLC) system.
Lin SY; Chien SC; Su YN; Lee CN; Chen CP
Prenat Diagn; 2006 May; 26(5):466-70. PubMed ID: 16570240
[TBL] [Abstract][Full Text] [Related]
10. Identification and in silico characterization of p.G380R substitution in FGFR3, associated with achondroplasia in a non-consanguineous Pakistani family.
Ajmal M; Mir A; Shoaib M; Malik SA; Nasir M
Diagn Pathol; 2017 Jul; 12(1):47. PubMed ID: 28679403
[TBL] [Abstract][Full Text] [Related]
11. [Detection of fibroblast growth factor receptor 3 gene mutation at nucleotide 1138 site in congenita achondroplasia patients].
Ni J; Lu G; Wang W; Chen F; Qin H; Wang D
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Jun; 19(3):205-8. PubMed ID: 12048679
[TBL] [Abstract][Full Text] [Related]
12. [Mutation analysis of fibroblast growth factor receptor 3 gene in an achondroplasia family].
Zhu B; Dong QM; Huang XH; Ji GQ; Chen Y; Wang WX; Jiang HY; Gao JS
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Oct; 20(5):373-5. PubMed ID: 14556186
[TBL] [Abstract][Full Text] [Related]
13. [Rapid prenatal genetic diagnosis of a fetus with a high risk for Morquio A syndrome].
Guo YB; Ai Y; Zhao Y; Tang J; Jiang WY; Du ML; Ma HM; Zhong YF
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Apr; 29(2):126-30. PubMed ID: 22487817
[TBL] [Abstract][Full Text] [Related]
14. [Prenatal diagnosis of oculocutaneous albinism type II and discovery of two novel mutations].
Li HY; Wei HY; Zheng H; Meng S; Jiang WY; Chen LM; Duan HL
Zhonghua Yi Xue Za Zhi; 2007 Apr; 87(16):1123-5. PubMed ID: 17672996
[TBL] [Abstract][Full Text] [Related]
15. [Genetic analysis and prenatal diagnosis for a family with megalencephalic leukoencephalopathy and subcortical cysts].
Wu WQ; Xie JS; Han CX; Xu ZY; Geng Q; Yuan H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):616-9. PubMed ID: 22161090
[TBL] [Abstract][Full Text] [Related]
16. Genotyping of the G1138A mutation of the FGFR3 gene in patients with achondroplasia using high-resolution melting analysis.
Hung CC; Lee CN; Chang CH; Jong YJ; Chen CP; Hsieh WS; Su YN; Lin WL
Clin Biochem; 2008 Feb; 41(3):162-6. PubMed ID: 18199430
[TBL] [Abstract][Full Text] [Related]
17. Prenatal DNA diagnosis of a single-gene disorder from maternal plasma.
Saito H; Sekizawa A; Morimoto T; Suzuki M; Yanaihara T
Lancet; 2000 Sep; 356(9236):1170. PubMed ID: 11030304
[TBL] [Abstract][Full Text] [Related]
18. [Application of multiplex quantitative fluorescent PCR with non-polymorphic loci in prenatal diagnosis].
Zhu XY; Hu YL; Wang YP; Zhu HY; Li J; Zhu RF; Zhang Y; Wu X; Yang Y
Zhonghua Fu Chan Ke Za Zhi; 2008 Nov; 43(11):818-23. PubMed ID: 19087563
[TBL] [Abstract][Full Text] [Related]
19. Rapid detection of FGFR3 gene mutation in achondroplasia by DHPLC system-coupling heteroduplex and fluorescence-enhanced primer-extension analysis.
Su YN; Lee CN; Chien SC; Hung CC; Chien YH; Chen CA
J Hum Genet; 2004; 49(8):399-403. PubMed ID: 15221641
[TBL] [Abstract][Full Text] [Related]
20. [Denaturing high-performance liquid chromatography for screening antithrombin III gene mutation and polymorphisms in patients with cerebral venous thrombosis].
Wang LP; Qiu YW; Yin AL; Ma YY; Liu KL; Xiong L; Yu YH; Zhong M; Wang C
Nan Fang Yi Ke Da Xue Xue Bao; 2009 Oct; 29(10):1982-6. PubMed ID: 19861246
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
