111 related articles for article (PubMed ID: 8981154)
1. Rapid genetic diagnosis at 7-9 weeks gestation: diagnosis of sex, single gene defects and DNA fingerprint from coelomic samples.
Findlay I; Atkinson G; Chambers M; Quirke P; Campbell J; Rutherford A
Hum Reprod; 1996 Nov; 11(11):2548-53. PubMed ID: 8981154
[TBL] [Abstract][Full Text] [Related]
2. Very early prenatal diagnosis of Cockayne's syndrome by coelocentesis.
Giambona A; Vinciguerra M; Leto F; Cassarà F; Cucinella G; Cigna V; Orlandi E; Piccione M; Picciotto F; Maggio A
J Obstet Gynaecol; 2022 Jul; 42(5):1524-1531. PubMed ID: 35006018
[TBL] [Abstract][Full Text] [Related]
3. Coelocentesis: a new technique for early prenatal diagnosis.
Jurkovic D; Jauniaux E; Campbell S; Pandya P; Cardy DL; Nicolaides KH
Lancet; 1993 Jun; 341(8861):1623-4. PubMed ID: 8099993
[TBL] [Abstract][Full Text] [Related]
4. Prenatal paternity testing using DNA extracted from coelomic cells.
Makrydimas G; Georgiou I; Kranas V; Kaponis A; Lolis D
Fetal Diagn Ther; 2004; 19(1):75-7. PubMed ID: 14646423
[TBL] [Abstract][Full Text] [Related]
5. Circulating trophoblastic cells provide genetic diagnosis in 63 fetuses at risk for cystic fibrosis or spinal muscular atrophy.
Mouawia H; Saker A; Jais JP; Benachi A; Bussières L; Lacour B; Bonnefont JP; Frydman R; Simpson JL; Paterlini-Brechot P
Reprod Biomed Online; 2012 Nov; 25(5):508-20. PubMed ID: 23000084
[TBL] [Abstract][Full Text] [Related]
6. Very early prenatal diagnosis of genetic diseases based on coelomic fluid analysis: a feasibility study.
Jouannic JM; Costa JM; Ernault P; Bénifla JL
Hum Reprod; 2006 Aug; 21(8):2185-8. PubMed ID: 16769753
[TBL] [Abstract][Full Text] [Related]
7. Simultaneous DNA 'fingerprinting', diagnosis of sex and single-gene defect status from single cells.
Findlay I; Urquhart A; Quirke P; Sullivan K; Rutherford AJ; Lilford RJ
Hum Reprod; 1995 Apr; 10(4):1005-13. PubMed ID: 7650110
[TBL] [Abstract][Full Text] [Related]
8. A study of fetal sex determination in coelomic fluid.
Lau TK; Fung TY; Wong YF; Fung HY
Gynecol Obstet Invest; 1998; 45(1):16-8. PubMed ID: 9473157
[TBL] [Abstract][Full Text] [Related]
9. Aneuploidy screening in coelomic samples using fluorescence in situ hybridisation (FISH).
Chatzimeletiou K; Makrydimas G; Sotiriadis A; Paraskevaidis E; Nicolaides KH
Prenat Diagn; 2005 Oct; 25(10):919-26. PubMed ID: 16103986
[TBL] [Abstract][Full Text] [Related]
10. Early prenatal diagnosis: standard cytogenetic analysis of coelomic cells obtained by coelocentesis.
Crüger DG; Bruun-Petersen G; Kølvraa S
Prenat Diagn; 1996 Oct; 16(10):945-9. PubMed ID: 8938067
[TBL] [Abstract][Full Text] [Related]
11. [Chorionic villus needle sampling by the transabdominal route or by placental centesis. A series of 930 cases].
Guidicelli B; Levy A; Piquet C; Gamerre M
J Gynecol Obstet Biol Reprod (Paris); 1993; 22(8):851-5. PubMed ID: 8132961
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis of beta-thalassaemia by coelocentesis.
Makrydimas G; Georgiou I; Kranas V; Zikopoulos K; Lolis D
Mol Hum Reprod; 1997 Aug; 3(8):729-31. PubMed ID: 9294859
[TBL] [Abstract][Full Text] [Related]
13. Fluorescent PCR: a new technique for PGD of sex and single-gene defects.
Findlay I; Quirke P; Hall J; Rutherford A
J Assist Reprod Genet; 1996 Feb; 13(2):96-103. PubMed ID: 8688597
[TBL] [Abstract][Full Text] [Related]
14. Clinical application of fetal sex determination using cell-free fetal DNA in pregnant carriers of X-linked genetic disorders.
Miura K; Higashijima A; Shimada T; Miura S; Yamasaki K; Abe S; Jo O; Kinoshita A; Yoshida A; Yoshimura S; Niikawa N; Yoshiura K; Masuzaki H
J Hum Genet; 2011 Apr; 56(4):296-9. PubMed ID: 21307866
[TBL] [Abstract][Full Text] [Related]
15. The safety and efficacy of chorionic villus sampling for early prenatal diagnosis of cytogenetic abnormalities.
Rhoads GG; Jackson LG; Schlesselman SE; de la Cruz FF; Desnick RJ; Golbus MS; Ledbetter DH; Lubs HA; Mahoney MJ; Pergament E
N Engl J Med; 1989 Mar; 320(10):609-17. PubMed ID: 2645520
[TBL] [Abstract][Full Text] [Related]
16. Use of a DNA method, QF-PCR, in the prenatal diagnosis of fetal aneuploidies.
Langlois S; Duncan A; ;
J Obstet Gynaecol Can; 2011 Sep; 33(9):955-960. PubMed ID: 21923994
[TBL] [Abstract][Full Text] [Related]
17. Chorionic villus sampling (CVS) and fluorescence in situ hybridization (FISH) for a rapid first-trimester prenatal diagnosis.
Goumy C; Bonnet-Dupeyron MN; Cherasse Y; Laurichesse H; Jaffray JY; Lacroute G; Geneix A; Lemery D; Vago P
Prenat Diagn; 2004 Apr; 24(4):249-56. PubMed ID: 15065097
[TBL] [Abstract][Full Text] [Related]
18. Non-invasive prenatal diagnosis (NIPD) of cystic fibrosis: an optimized protocol using MEMO fluorescent PCR to detect the p.Phe508del mutation.
Guissart C; Dubucs C; Raynal C; Girardet A; Tran Mau Them F; Debant V; Rouzier C; Boureau-Wirth A; Haquet E; Puechberty J; Bieth E; Dupin Deguine D; Khau Van Kien P; Brechard MP; Pritchard V; Koenig M; Claustres M; Vincent MC
J Cyst Fibros; 2017 Mar; 16(2):198-206. PubMed ID: 28040480
[TBL] [Abstract][Full Text] [Related]
19. Prenatal cytogenetic diagnosis study of 2782 cases of high-risk pregnant women.
Zhang L; Zhang XH; Liang MY; Ren MH
Chin Med J (Engl); 2010 Feb; 123(4):423-30. PubMed ID: 20193481
[TBL] [Abstract][Full Text] [Related]
20. [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]
[Next] [New Search]
