-
1
-
-
33748127084
-
Regional variations in prenatal screening across Australia: Stepping towards a national policy framework
-
O'Leary P, Breheny N, Reid G, Charles T, Emery J. Regional variations in prenatal screening across Australia: Stepping towards a national policy framework. Aust N Z J Obstet Gynaecol 2006; 46: 427-432.
-
(2006)
Aust N Z J Obstet Gynaecol
, vol.46
, pp. 427-432
-
-
O'Leary, P.1
Breheny, N.2
Reid, G.3
Charles, T.4
Emery, J.5
-
2
-
-
8844221276
-
The introduction of QF-PCR in prenatal diagnosis of fetal aneuploidies: Time for reconsideration
-
Nicolini U, Lalatta F, Natacci F, Curcio C, Bui T-H. The introduction of QF-PCR in prenatal diagnosis of fetal aneuploidies: Time for reconsideration. Hum Reprod Update 2004; 10: 541-548.
-
(2004)
Hum Reprod Update
, vol.10
, pp. 541-548
-
-
Nicolini, U.1
Lalatta, F.2
Natacci, F.3
Curcio, C.4
Bui, T.-H.5
-
3
-
-
0017316806
-
Midtrimester amniocentesis for prenatal diagnosis. Safety and accuracy
-
National Institute of Child Health and Human Development
-
National Institute of Child Health and Human Development. Midtrimester amniocentesis for prenatal diagnosis. Safety and accuracy. JAMA 1976; 236: 1471-1476.
-
(1976)
JAMA
, vol.236
, pp. 1471-1476
-
-
-
4
-
-
0024522992
-
The safety and efficacy of chorionic villus sampling for early prenatal diagnosis of cytogenetic abnormalities
-
Rhoads GC, Jackson LG, Schlesselman SE et al. The safety and efficacy of chorionic villus sampling for early prenatal diagnosis of cytogenetic abnormalities. N Engl J Med 1989; 320: 609-617.
-
(1989)
N Engl J Med
, vol.320
, pp. 609-617
-
-
Rhoads, G.C.1
Jackson, L.G.2
Schlesselman, S.E.3
-
5
-
-
0030986393
-
Accuracy of cytogenetic findings on chorionic villus sampling (CVS) - Diagnostic consequences of CVS mosaicism and non-mosaic discrepancy in centres contributing to EUCROMIC 1986-92
-
Hahnemann JM, Vejerslev LO. Accuracy of cytogenetic findings on chorionic villus sampling (CVS) - Diagnostic consequences of CVS mosaicism and non-mosaic discrepancy in centres contributing to EUCROMIC 1986-92. Prenat Diagn 1997; 17: 801-820.
-
(1997)
Prenat Diagn
, vol.17
, pp. 801-820
-
-
Hahnemann, J.M.1
Vejerslev, L.O.2
-
6
-
-
7944238741
-
Prenatal diagnosis by rapid aneuploidy detection and karyotyping: A prospective study of the role of ultrasound in 1589 second-trimester amniocenteses
-
Leung WC, Waters JJ, Chitty L. Prenatal diagnosis by rapid aneuploidy detection and karyotyping: A prospective study of the role of ultrasound in 1589 second-trimester amniocenteses. Prenat Diagn 2004; 24: 790-795.
-
(2004)
Prenat Diagn
, vol.24
, pp. 790-795
-
-
Leung, W.C.1
Waters, J.J.2
Chitty, L.3
-
7
-
-
0141613852
-
Rapid and simple prenatal diagnosis of common chromosome disorders
-
Advantages and disadvantages of the molecular methods FISH and QF-PCR
-
Hultén MA, Dhanjal S, Pertl B. Rapid and simple prenatal diagnosis of common chromosome disorders. Advantages and disadvantages of the molecular methods FISH and QF-PCR. Reproduction 2003; 126: 279-297.
-
(2003)
Reproduction
, vol.126
, pp. 279-297
-
-
Hultén, M.A.1
Dhanjal, S.2
Pertl, B.3
-
8
-
-
22244465516
-
Prenatal detection of Down's syndrome by rapid aneuploidy testing for chromosomes 13, 18, and 21 by FISH or PCR without a full karyotype: A cytogenetic risk assessment
-
Caine A, Maltby AE, Parkin CA et al. Prenatal detection of Down's syndrome by rapid aneuploidy testing for chromosomes 13, 18, and 21 by FISH or PCR without a full karyotype: A cytogenetic risk assessment. Lancet 2005; 366: 123-128.
-
(2005)
Lancet
, vol.366
, pp. 123-128
-
-
Caine, A.1
Maltby, A.E.2
Parkin, C.A.3
-
9
-
-
33749573864
-
Rapid prenatal diagnosis by QF-PCR: Evaluation of 30 000 consecutive clinical samples and future applications
-
Cirigliano V, Voglino G, Marongiu A et al. Rapid prenatal diagnosis by QF-PCR: Evaluation of 30 000 consecutive clinical samples and future applications. Ann N Y Acad Sci 2006; 1075: 288-298.
-
(2006)
Ann N Y Acad Sci
, vol.1075
, pp. 288-298
-
-
Cirigliano, V.1
Voglino, G.2
Marongiu, A.3
-
10
-
-
33846406009
-
Ultrasound findings before amniocentesis in selecting the method of analysing the sample
-
Kagan KO, Chitty LS, Cicero S, Eleftheriades M, Nicolaides KH. Ultrasound findings before amniocentesis in selecting the method of analysing the sample. Prenat Diagn 2007; 27: 34-39.
-
(2007)
Prenat Diagn
, vol.27
, pp. 34-39
-
-
Kagan, K.O.1
Chitty, L.S.2
Cicero, S.3
Eleftheriades, M.4
Nicolaides, K.H.5
-
11
-
-
0020621218
-
Efficient direct chromosome analyses and enzyme determinations from chorionic villus samples in the first trimester of pregnancy
-
Simoni G, Brambati B, Danesino C et al. Efficient direct chromosome analyses and enzyme determinations from chorionic villus samples in the first trimester of pregnancy. Hum Genet 1983; 63: 349-357.
-
(1983)
Hum Genet
, vol.63
, pp. 349-357
-
-
Simoni, G.1
Brambati, B.2
Danesino, C.3
-
12
-
-
41649096129
-
Rapid aneuploidy testing versus traditional karyotyping: Is it better to know more?
-
Leung TN. Rapid aneuploidy testing versus traditional karyotyping: Is it better to know more? Hong Kong Med J 2008; 14: 4-5.
-
(2008)
Hong Kong Med J
, vol.14
, pp. 4-5
-
-
Leung, T.N.1
-
13
-
-
0032951503
-
International, collaborative assessment of 146 000 prenatal karyotypes: Expected limitations if only chromosome-specific probes and fluorescent in situ hybridization are used
-
Evans MI, Henry GP, Miller WA et al. International, collaborative assessment of 146 000 prenatal karyotypes: Expected limitations if only chromosome-specific probes and fluorescent in situ hybridization are used. Hum Reprod 1999; 14: 1213-1216.
-
(1999)
Hum Reprod
, vol.14
, pp. 1213-1216
-
-
Evans, M.I.1
Henry, G.P.2
Miller, W.A.3
-
14
-
-
42049112787
-
Optimized criteria for using fluorescence in situ hybridization in the prenatal diagnosis of common aneuploidies
-
Leclercq S, Lebbar A, Grange G et al. Optimized criteria for using fluorescence in situ hybridization in the prenatal diagnosis of common aneuploidies. Prenat Diagn 2008; 28: 313-318.
-
(2008)
Prenat Diagn
, vol.28
, pp. 313-318
-
-
Leclercq, S.1
Lebbar, A.2
Grange, G.3
-
15
-
-
41649104904
-
Rapid aneuploidy testing (knowing less) versus traditional karyotyping (knowing more) for advanced maternal age: What would be missed, who should decide?
-
Leung WC, Lau ET, Lau WL et al. Rapid aneuploidy testing (knowing less) versus traditional karyotyping (knowing more) for advanced maternal age: What would be missed, who should decide? Hong Kong Med J 2008; 14: 6-13.
-
(2008)
Hong Kong Med J
, vol.14
, pp. 6-13
-
-
Leung, W.C.1
Lau, E.T.2
Lau, W.L.3
-
16
-
-
20444468193
-
Prospective first-trimester screening for trisomy 21 in 30 564 pregnancies
-
Avgidou K, Papageorghiou A, Bindra R, Spencer K, Nicolaides KH. Prospective first-trimester screening for trisomy 21 in 30 564 pregnancies. Am J Obstet Gynecol 2005; 192: 1761-1767.
-
(2005)
Am J Obstet Gynecol
, vol.192
, pp. 1761-1767
-
-
Avgidou, K.1
Papageorghiou, A.2
Bindra, R.3
Spencer, K.4
Nicolaides, K.H.5
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