234 related articles for article (PubMed ID: 26850935)
1. Droplet digital PCR combined with minisequencing, a new approach to analyze fetal DNA from maternal blood: application to the non-invasive prenatal diagnosis of achondroplasia.
Orhant L; Anselem O; Fradin M; Becker PH; Beugnet C; Deburgrave N; Tafuri G; Letourneur F; Goffinet F; Allach El Khattabi L; Leturcq F; Bienvenu T; Tsatsaris V; Nectoux J
Prenat Diagn; 2016 May; 36(5):397-406. PubMed ID: 26850935
[TBL] [Abstract][Full Text] [Related]
2. Non-invasive prenatal detection of achondroplasia using circulating fetal DNA in maternal plasma.
Lim JH; Kim MJ; Kim SY; Kim HO; Song MJ; Kim MH; Park SY; Yang JH; Ryu HM
J Assist Reprod Genet; 2011 Feb; 28(2):167-72. PubMed ID: 20963478
[TBL] [Abstract][Full Text] [Related]
3. Optimal non-invasive diagnosis of fetal achondroplasia combining ultrasonography with circulating cell-free fetal DNA analysis.
Vivanti AJ; Costa JM; Rosefort A; Kleinfinger P; Lohmann L; Cordier AG; Benachi A
Ultrasound Obstet Gynecol; 2019 Jan; 53(1):87-94. PubMed ID: 29380944
[TBL] [Abstract][Full Text] [Related]
4. Non-invasive prenatal detection of achondroplasia in size-fractionated cell-free DNA by MALDI-TOF MS assay.
Li Y; Page-Christiaens GC; Gille JJ; Holzgreve W; Hahn S
Prenat Diagn; 2007 Jan; 27(1):11-7. PubMed ID: 17154237
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. [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]
7. Non-invasive prenatal diagnosis of achondroplasia and thanatophoric dysplasia: next-generation sequencing allows for a safer, more accurate, and comprehensive approach.
Chitty LS; Mason S; Barrett AN; McKay F; Lench N; Daley R; Jenkins LA
Prenat Diagn; 2015 Jul; 35(7):656-62. PubMed ID: 25728633
[TBL] [Abstract][Full Text] [Related]
8. A novel non-invasive detection method for the FGFR3 gene mutation in maternal plasma for a fetal achondroplasia diagnosis based on signal amplification by hemin-MOFs/PtNPs.
Chen J; Yu C; Zhao Y; Niu Y; Zhang L; Yu Y; Wu J; He J
Biosens Bioelectron; 2017 May; 91():892-899. PubMed ID: 27836589
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. Multiplex PCR in noninvasive prenatal diagnosis for FGFR3-related disorders.
Terasawa S; Kato A; Nishizawa H; Kato T; Yoshizawa H; Noda Y; Miyazaki J; Ito M; Sekiya T; Fujii T; Kurahashi H
Congenit Anom (Kyoto); 2019 Jan; 59(1):4-10. PubMed ID: 29542187
[TBL] [Abstract][Full Text] [Related]
11. Droplet digital PCR, a new approach to analyze fetal DNA from maternal blood: application to the determination of fetal RHD genotype.
Orhant L; Rondeau S; Vasson A; Anselem O; Goffinet F; Allach El Khattabi L; Leturcq F; Vidaud D; Bienvenu T; Tsatsaris V; Nectoux J
Ann Biol Clin (Paris); 2016 Jun; 74(3):269-77. PubMed ID: 27237800
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. New aids for the non-invasive prenatal diagnosis of achondroplasia: dysmorphic features, charts of fetal size and molecular confirmation using cell-free fetal DNA in maternal plasma.
Chitty LS; Griffin DR; Meaney C; Barrett A; Khalil A; Pajkrt E; Cole TJ
Ultrasound Obstet Gynecol; 2011 Mar; 37(3):283-9. PubMed ID: 21105021
[TBL] [Abstract][Full Text] [Related]
14. Ultrasound and molecular mid-trimester prenatal diagnosis of de novo achondroplasia.
Mesoraca A; Pilu G; Perolo A; Novelli G; Salfi N; Lucchi A; Bovicelli L; Dallapiccola B
Prenat Diagn; 1996 Aug; 16(8):764-8. PubMed ID: 8878289
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. [Clinical application of noninvasive prenatal diagnosis using cell free fetal DNA in maternal plasma].
Hou QF; Wu D; Chu Y; Kang B; Liao SX; Yang YL; Zhang CY; Zhang JX; Wu G
Zhonghua Fu Chan Ke Za Zhi; 2012 Nov; 47(11):813-7. PubMed ID: 23302120
[TBL] [Abstract][Full Text] [Related]
17. Non-Invasive Prenatal Diagnosis of Lethal Skeletal Dysplasia by Targeted Capture Sequencing of Maternal Plasma.
Dan S; Yuan Y; Wang Y; Chen C; Gao C; Yu S; Liu Y; Song W; Asan ; Zhu H; Yang L; Deng H; Su Y; Yi X
PLoS One; 2016; 11(7):e0159355. PubMed ID: 27433940
[TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of achondroplasia presenting with multiple-suture synostosis: a novel association.
Karadimas C; Trouvas D; Haritatos G; Makatsoris C; Dedoulis E; Velissariou V; Antoniadi T; Hatzaki A; Petersen MB
Prenat Diagn; 2006 Mar; 26(3):258-61. PubMed ID: 16475234
[TBL] [Abstract][Full Text] [Related]
19. Application of real-time PCR of sex-independent insertion-deletion polymorphisms to determine fetal sex using cell-free fetal DNA from maternal plasma.
Ho SS; Barrett A; Thadani H; Asibal CL; Koay ES; Choolani M
Clin Chem Lab Med; 2015 Jul; 53(8):1189-95. PubMed ID: 25581758
[TBL] [Abstract][Full Text] [Related]
20. Prenatal ultrasound and MRI findings of temporal and occipital lobe dysplasia in a twin with achondroplasia.
Pugash D; Lehman AM; Langlois S
Ultrasound Obstet Gynecol; 2014 Sep; 44(3):365-8. PubMed ID: 24616001
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
