-
1
-
-
67149115401
-
Clinical practice. Prenatal screening for aneuploidy
-
Driscoll D, Gross S. Clinical practice. Prenatal screening for aneuploidy. N Eng J Med. 2009, 360, 2556-2562.
-
(2009)
N Eng J Med.
, vol.360
, pp. 2556-2562
-
-
Driscoll, D.1
Gross, S.2
-
2
-
-
0027936511
-
Maternal age-specific risks for trisomies at 9-14 weeks' gestation
-
Snijders R, Holzgreve W, Cuckle H, Nicolaides K. Maternal age-specific risks for trisomies at 9-14 weeks' gestation. Prenat Diagn. 1994, 14, 543-552.
-
(1994)
Prenat Diagn.
, vol.14
, pp. 543-552
-
-
Snijders, R.1
Holzgreve, W.2
Cuckle, H.3
Nicolaides, K.4
-
3
-
-
78349280822
-
Two-stage first-trimester screening for trisomy 21 by ultrasound assessment and biochemical testing
-
Kagan K, Staboulidou I, Cruz J, [et al.]. Two-stage first-trimester screening for trisomy 21 by ultrasound assessment and biochemical testing. Ultrasound Obstet Gynecol. 2010, 36, 542- 547.
-
(2010)
Ultrasound Obstet Gynecol.
, vol.36
-
-
Kagan, K.1
Staboulidou, I.2
Cruz, J.3
-
4
-
-
78650803485
-
Screening for fetal aneuploides at 11 to 13 weeks
-
Nicolaides KH. Screening for fetal aneuploides at 11 to 13 weeks. Prenat Diagn. 2011, 31, 7-15.
-
(2011)
Prenat Diagn.
, vol.31
, pp. 7-15
-
-
Nicolaides, K.H.1
-
5
-
-
68949189360
-
Rekomendacje Polskiego Towarzystwa Ginekologicznego dotyczace postepowania w zakresie diagnostyki prenatalnej
-
Rekomendacje Zespolu Ekspertów PTG
-
Rekomendacje Zespolu Ekspertów PTG. Rekomendacje Polskiego Towarzystwa Ginekologicznego dotyczace postepowania w zakresie diagnostyki prenatalnej. Ginekol Pol. 2009, 80, 390-393.
-
(2009)
Ginekol Pol.
, vol.80
, pp. 390-393
-
-
-
6
-
-
84856678436
-
Pregnancy outcome following mid-trimester amniocentesis
-
Corrado F, Cannata M, La Galia T, [et al.]. Pregnancy outcome following mid-trimester amniocentesis. J Obstet Gynaecol. 2012, 32, 117-119.
-
(2012)
J Obstet Gynaecol.
, vol.32
, pp. 117-119
-
-
Corrado, F.1
Cannata, M.2
La Galia, T.3
-
7
-
-
34548405957
-
Procedure-related complications of amniocentesis and chorionic villus sampling
-
Mujenovic F, Alfirevic Z. Procedure-related complications of amniocentesis and chorionic villus sampling. Obstet Gynecol. 2007, 110, 687-694.
-
(2007)
Obstet Gynecol.
, vol.110
, pp. 687-694
-
-
Mujenovic, F.1
Alfirevic, Z.2
-
8
-
-
84859350834
-
Noninvasive prenatal testing for aneuploidy-ready for prime time?
-
Chitty L, Hill M, White H, [et al.]. Noninvasive prenatal testing for aneuploidy-ready for prime time? Am J Obstet Gynecol. 2012, 206, 269-275.
-
(2012)
Am J Obstet Gynecol
, vol.206
, pp. 269-275
-
-
Chitty, L.1
Hill, M.2
White, H.3
-
9
-
-
0014666881
-
Practical and theoretical implications of fetal-maternal lymphocyte transfer
-
Walknowska J, Conte F, Grumbach M. Practical and theoretical implications of fetal-maternal lymphocyte transfer. Lancet 1969, 1, 1119-1122.
-
(1969)
Lancet
, vol.1
, pp. 1119-1122
-
-
Walknowska, J.1
Conte, F.2
Grumbach, M.3
-
10
-
-
0036635237
-
Fetal gender and aneuploidy detection using fetal cells in maternal blood: analysis of NIFTY I data
-
Bianchi D, Simpson J, Jackson L, [et al.]. Fetal gender and aneuploidy detection using fetal cells in maternal blood: analysis of NIFTY I data. Prenat Diagn. 2002, 22, 609-615.
-
(2002)
Prenat Diagn.
, vol.22
, pp. 609-615
-
-
Bianchi, D.1
Simpson, J.2
Jackson, L.3
-
11
-
-
84455169920
-
Fetal microchimetric cells in blond of women with an autoimmune thyroid disease
-
Lepez T, Vandewostyne M, Hussain S, [et al.]. Fetal microchimetric cells in blond of women with an autoimmune thyroid disease. PLoS One. 2011, 6, e29646.
-
(2011)
PLoS One.
, vol.6
-
-
Lepez, T.1
Vandewostyne, M.2
Hussain, S.3
-
12
-
-
0014054213
-
Life-span of fetal red blood cell
-
Pearson H. Life-span of fetal red blood cell. J Pediatr 1967, 70, 166-171.
-
(1967)
J Pediatr
, vol.70
, pp. 166-171
-
-
Pearson, H.1
-
13
-
-
0030034519
-
Male fetal progenitor cells persist in maternal blood for as long as 27 years postpartum
-
Bianchi D, Zickwolf G, Weil G, [et al.].. Male fetal progenitor cells persist in maternal blood for as long as 27 years postpartum. Proc Natl Acad Sci U S A. 1996, 93, 705-708.
-
(1996)
Proc Natl Acad Sci U S A.
, vol.93
, pp. 705-708
-
-
Bianchi, D.1
Zickwolf, G.2
Weil, G.3
-
14
-
-
0030776456
-
PCR quantitation of fetal cells in maternal blood in normal and aneuploid pregnancies
-
Bianchi D, Williams J, Sullivan L, [et al.]. PCR quantitation of fetal cells in maternal blood in normal and aneuploid pregnancies. Am J Hum Genet. 1997, 61, 822-829.
-
(1997)
Am J Hum Genet.
, vol.61
, pp. 822-829
-
-
Bianchi, D.1
Williams, J.2
Sullivan, L.3
-
15
-
-
84865463511
-
The promise of fetal cells in maternal blood
-
Choolani M. The promise of fetal cells in maternal blood. B Pract Res Clin Obstet Gynecol. 2012, 26, 655-667.
-
(2012)
B Pract Res Clin Obstet Gynecol.
, vol.26
, pp. 655-667
-
-
Choolani, M.1
-
16
-
-
0342618532
-
Presence of fetal DNA in maternal plasma and serum
-
Lo YM, Corbetta N, Chamberlain P, [et al.]. Presence of fetal DNA in maternal plasma and serum. Lancet. 1997, 350, 485-487.
-
(1997)
Lancet.
, vol.350
, pp. 485-487
-
-
Lo, Y.M.1
Corbetta, N.2
Chamberlain, P.3
-
17
-
-
84872871232
-
Recent advances in the prenatal interrogation of the human fetal genome
-
Hui L, Bianchi D. Recent advances in the prenatal interrogation of the human fetal genome. Trends Genet. 2013, 29, 84-91.
-
(2013)
Trends Genet.
, vol.29
, pp. 84-91
-
-
Hui, L.1
Bianchi, D.2
-
18
-
-
1942487331
-
Circulating fetal DNA: its origin and diagnostics potential-a review
-
Bianchi D. Circulating fetal DNA: its origin and diagnostics potential-a review. Placenta. 2004, 25, Suppl. A, S93-S101.
-
(2004)
Placenta.
, vol.25
, Issue.SUPPL. A
-
-
Bianchi, D.1
-
19
-
-
84864408781
-
Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study or detection of fetal trisomy 21 and trisomy 18
-
Norton M, Brar H, Weiss J, [et al.]. Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study or detection of fetal trisomy 21 and trisomy 18. Am J Obstet Gynecol. 2012, 207, 137.e1-8.
-
(2012)
Am J Obstet Gynecol.
, vol.207
-
-
Norton, M.1
Brar, H.2
Weiss, J.3
-
20
-
-
0347898005
-
Quantitative analysis of fetal DNA in maternal plasma and serum: Implications for noninvasive prenatal diagnosis
-
Lo Y. Quantitative analysis of fetal DNA in maternal plasma and serum: Implications for noninvasive prenatal diagnosis. Am J Hum Genet. 1998, 62, 768-775.
-
(1998)
Am J Hum Genet.
, vol.62
, pp. 768-775
-
-
Lo, Y.1
-
21
-
-
0033364339
-
Rapid clearance of fetal DNA from maternal plasma
-
Lo YMD, Zhang J, Leung TN, [et al.]. Rapid clearance of fetal DNA from maternal plasma. Am J Hum Genet. 1999, 64, 218-224.
-
(1999)
Am J Hum Genet.
, vol.64
, pp. 218-224
-
-
Lo, Y.M.D.1
Zhang, J.2
Leung, T.N.3
-
22
-
-
85010301450
-
Cell-free fetal DNA is not present in plasma of nonpregnant mothers
-
Rijnders R, Christiaens G, Soussan A, van der Schoot C. Cell-free fetal DNA is not present in plasma of nonpregnant mothers. Clin Chem. 2004, 50, 697-681.
-
(2004)
Clin Chem.
, vol.50
, pp. 697-681
-
-
Rijnders, R.1
Christiaens, G.2
Soussan, A.3
van der Schoot, C.4
-
23
-
-
0036626528
-
Presence of fetal DNA in maternal plasma decades after pregnancy
-
Invernizzi P, Biondi M, Battezzati P, [et al.]. Presence of fetal DNA in maternal plasma decades after pregnancy. Hum Genet. 2002, 110, 587-591.
-
(2002)
Hum Genet.
, vol.110
, pp. 587-591
-
-
Invernizzi, P.1
Biondi, M.2
Battezzati, P.3
-
24
-
-
0034872431
-
Effects of blood-processing protocols on fetal ant total DNA quantification in Maternal plasma
-
Chiu R, Poon L, Leung T, [et al.]. Effects of blood-processing protocols on fetal ant total DNA quantification in Maternal plasma. Clin Chem. 2001, 47, 1607-1613.
-
(2001)
Clin Chem.
, vol.47
, pp. 1607-1613
-
-
Chiu, R.1
Poon, L.2
Leung, T.3
-
25
-
-
0032992867
-
Quantitative abnormalities of fetal DNA in maternal serum in preeclampsia
-
Lo Y, Leung T, Tein M, [et al.]. Quantitative abnormalities of fetal DNA in maternal serum in preeclampsia. Clin Chem. 1999, 45, 184-188.
-
(1999)
Clin Chem.
, vol.45
, pp. 184-188
-
-
Lo, Y.1
Leung, T.2
Tein, M.3
-
26
-
-
18744415967
-
Fetal DNA clearance from maternal plasma is impaired in preeclampsia
-
Lau T, Leung T, Chan L, [et al.]. Fetal DNA clearance from maternal plasma is impaired in preeclampsia. Clin Chem. 2002, 48, 2141-2146.
-
(2002)
Clin Chem.
, vol.48
, pp. 2141-2146
-
-
Lau, T.1
Leung, T.2
Chan, L.3
-
27
-
-
74049097228
-
Brojer E Nieinwazyjne badania prenatalne z osocza kobiet ciezarnych w konflikcie serologicznym w Polsce
-
Orzinska A, Guz K, Brojer E Nieinwazyjne badania prenatalne z osocza kobiet ciezarnych w konflikcie serologicznym w Polsce. Ginekol Pol. 2009, 80, 768-771.
-
(2009)
Ginekol Pol.
, vol.80
, pp. 768-771
-
-
Orzinska, A.1
Guz, K.2
-
28
-
-
0034818672
-
Fetal sex determination from maternal plasma in pregnancies at risk for congenital adrenal hyperplasia
-
Rijnders R, Schoot van der E, Bossers B, [et al.]. Fetal sex determination from maternal plasma in pregnancies at risk for congenital adrenal hyperplasia. Obstet Gynecol. 2001, 98, 374-378.
-
(2001)
Obstet Gynecol.
, vol.98
, pp. 374-378
-
-
Rijnders, R.1
Schoot van der, E.2
Bossers, B.3
-
29
-
-
58149316091
-
The use of maternal plasma for prenatal RhD blood group genotyping
-
Finning K, Martin P, Daniels G. The use of maternal plasma for prenatal RhD blood group genotyping. Methods Mol Biol. 2009, 496, 143-157.
-
(2009)
Methods Mol Biol.
, vol.496
, pp. 143-157
-
-
Finning, K.1
Martin, P.2
Daniels, G.3
-
30
-
-
0035154948
-
Increased Maternal plasma fetal DNA concentrations in women who eventually develop preeclampsia
-
Leung T, Zhang J, Lau T, [et al.]. Increased Maternal plasma fetal DNA concentrations in women who eventually develop preeclampsia. Clin Chem. 2001, 47, 137-139.
-
(2001)
Clin Chem.
, vol.47
, pp. 137-139
-
-
Leung, T.1
Zhang, J.2
Lau, T.3
-
31
-
-
0032512311
-
Maternal plasma fetal DNA as a maker for preterm labour
-
Leung T, Zhang J, Lau T, [et al.]. Maternal plasma fetal DNA as a maker for preterm labour. Lancet. 1998, 352, 1904-1905.
-
(1998)
Lancet.
, vol.352
, pp. 1904-1905
-
-
Leung, T.1
Zhang, J.2
Lau, T.3
-
32
-
-
0033968645
-
Prenatal diagnosis of myotonic dystrophy using fetal DNA obtained from maternal plasma
-
Amicucci P, Gennarelli M, Novelli G, [et al.]. Prenatal diagnosis of myotonic dystrophy using fetal DNA obtained from maternal plasma. Clin Chem. 2000, 46, 301-302.
-
(2000)
Clin Chem.
, vol.46
, pp. 301-302
-
-
Amicucci, P.1
Gennarelli, M.2
Novelli, G.3
-
33
-
-
0034734711
-
Prenatal DNA diagnosis of single gene disorder from maternal plasma
-
Saito H, Sekizawa A, Morimoto T, [et al.]. Prenatal DNA diagnosis of single gene disorder from maternal plasma. Lancet. 2000, 356, 1170.
-
(2000)
Lancet.
, vol.356
, pp. 1170
-
-
Saito, H.1
Sekizawa, A.2
Morimoto, T.3
-
34
-
-
0034054074
-
High sensitivity of fetal DNA in plasma compared to serum and nucleated cells using unnested PCR in maternal blood
-
Houfflin-Debarge V, O'Donnell H, Overton T, [et al.]. High sensitivity of fetal DNA in plasma compared to serum and nucleated cells using unnested PCR in maternal blood. Fetal Diagn Ther. 2000, 15, 102-107.
-
(2000)
Fetal Diagn Ther.
, vol.15
, pp. 102-107
-
-
Houfflin-Debarge, V.1
O'Donnell, H.2
Overton, T.3
-
35
-
-
13844269123
-
Detection of paternally inherited fetal point mutations for beta-thalassemia using size-fractionated cell-free DNA in maternal plasma
-
Li Y, Di Naro E, Vitucci A, [et al.]. Detection of paternally inherited fetal point mutations for beta-thalassemia using size-fractionated cell-free DNA in maternal plasma. JAMA. 2005, 293, 843-849.
-
(2005)
JAMA.
, vol.293
, pp. 843-849
-
-
Li, Y.1
Di Naro, E.2
Vitucci, A.3
-
36
-
-
35348999450
-
Detection of aneuploidy with digital polymerase chain reaction
-
Fan H, Quake S. Detection of aneuploidy with digital polymerase chain reaction. Anal Chem. 2007, 79, 7576-7579.
-
(2007)
Anal Chem.
, vol.79
, pp. 7576-7579
-
-
Fan, H.1
Quake, S.2
-
37
-
-
34548727890
-
Digital PCR for the molecular detection of fetal chromosomal aneuploidy
-
Lo Y, Lun F, Chan K, [et al.]. Digital PCR for the molecular detection of fetal chromosomal aneuploidy. Proc Natl Acad Sci USA. 2007, 104, 13116-13121.
-
(2007)
Proc Natl Acad Sci USA.
, vol.104
, pp. 13116-13121
-
-
Lo, Y.1
Lun, F.2
Chan, K.3
-
38
-
-
58149490683
-
Noninvasive Prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma
-
Rossa W, Chiu K, Allen Chan, [et al.]. Noninvasive Prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma Proc Natl Acad Sci USA. 2008, 105, 20458-20463.
-
(2008)
Proc Natl Acad Sci USA.
, vol.105
, pp. 20458-20463
-
-
Rossa, W.1
Chiu, K.2
Chan, A.3
-
39
-
-
34548727890
-
Digital PCR for the molecular detection of fetal chromosomal aneuploidy
-
Lo Y, Lun F, Chan K, [et al.]. Digital PCR for the molecular detection of fetal chromosomal aneuploidy. Proc Natl Acad Sci USA. 2007, 104, 13116-13121.
-
(2007)
Proc Natl Acad Sci USA.
, vol.104
, pp. 13116-13121
-
-
Lo, Y.1
Lun, F.2
Chan, K.3
-
40
-
-
55849124028
-
Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood
-
Fan H, Blumenfeld Y, Chitkara U, [et al.]. Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood. Proc Natl Acad Sci USA. 2008, 105, 16266-16271.
-
(2008)
Proc Natl Acad Sci USA.
, vol.105
, pp. 16266-16271
-
-
Fan, H.1
Blumenfeld, Y.2
Chitkara, U.3
-
41
-
-
84871532946
-
Trisomy 13 detection in the first trimester of pregnancy using a chromosome-selective cell-free DNA analysis method
-
Ashoor G, Syngelaki A, Wang E, [et al.]. Trisomy 13 detection in the first trimester of pregnancy using a chromosome-selective cell-free DNA analysis method. Ultrasound Obstet Gynecol. 2013, 41, 21-25.
-
(2013)
Ultrasound Obstet Gynecol.
, vol.41
, pp. 21-25
-
-
Ashoor, G.1
Syngelaki, A.2
Wang, E.3
-
42
-
-
79959937504
-
Noninvasive Prenatal Diagnosis of Fetal Trisomy 18 and Trisomy 13 by Maternal Plasma DNA Sequencing
-
Chen E, Chiu R, Sun H, [et al.]. Noninvasive Prenatal Diagnosis of Fetal Trisomy 18 and Trisomy 13 by Maternal Plasma DNA Sequencing. PLoS ONE. 2011, 6, e21791.
-
(2011)
PLoS ONE.
, vol.6
-
-
Chen, E.1
Chiu, R.2
Sun, H.3
-
43
-
-
84894891695
-
Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing
-
Liang D, Lv W, Wang H, [et al.]. Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing. Prenat Diagn. 2013, 32, 1225-1232.
-
(2013)
Prenat Diagn.
, vol.32
, pp. 1225-1232
-
-
Liang, D.1
Lv, W.2
Wang, H.3
-
44
-
-
84858996474
-
Diagnostic Accuracy of Noninvasive Detection of Fetal Trisomy 21 in Maternal Blood: A Systematic Review
-
Verweij E, van den Oever J, de Boer M, [et al.]. Diagnostic Accuracy of Noninvasive Detection of Fetal Trisomy 21 in Maternal Blood: A Systematic Review. Fetal Diagn Ther. 2012, 31, 81-86.
-
(2012)
Fetal Diagn Ther.
, vol.31
, pp. 81-86
-
-
Verweij, E.1
van den Oever, J.2
de Boer, M.3
-
45
-
-
84879440410
-
Clinical application of massively parallel sequencing-based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11 105 pregnancies with mixed risk factors
-
Dan S, Wang W, Ren J, [et al.]. Clinical application of massively parallel sequencing-based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11 105 pregnancies with mixed risk factors. Prenat Diagn. 2012, 9, 1-8.
-
(2012)
Prenat Diagn.
, vol.9
, pp. 1-8
-
-
Dan, S.1
Wang, W.2
Ren, J.3
-
46
-
-
84859320067
-
Chromosome-selective sequencing of maternal plasma cell-free DNA for first-trimester detection of trisomy 21 and trisomy 18
-
Ashoor G, Syngelaki A, Wagner M, [et al.]. Chromosome-selective sequencing of maternal plasma cell-free DNA for first-trimester detection of trisomy 21 and trisomy 18. Am J Obstet Gynecol. 2012, 206, 322.e1-5.
-
(2012)
Am J Obstet Gynecol.
, vol.206
-
-
Ashoor, G.1
Syngelaki, A.2
Wagner, M.3
-
47
-
-
84857868297
-
DNA sequencing of maternal plasma reliably identiies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study
-
Palomaki G, Deciu C, Kloza E, [et al.]. DNA sequencing of maternal plasma reliably identiies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study. Genet Med. 2012, 14, 296-305.
-
(2012)
Genet Med.
, vol.14
, pp. 296-305
-
-
Palomaki, G.1
Deciu, C.2
Kloza, E.3
-
48
-
-
84871532946
-
Trisomy 13 detection in the first trimester of pregnancy using a chromosome - selective cell - freee DNA analysis method
-
Ashoor A, Syngelaki A, Wang E, [et al.]. Trisomy 13 detection in the first trimester of pregnancy using a chromosome - selective cell - freee DNA analysis method. Ultrasound Obstet Gynecol. 2013, 41, 21-25.
-
(2013)
Ultrasound Obstet Gynecol.
, vol.41
, pp. 21-25
-
-
Ashoor, A.1
Syngelaki, A.2
Wang, E.3
-
49
-
-
84868029481
-
Noninvasive prenatal testing for fetal trisomies in a routinely screened first-trimester population
-
Nicolaides K, Syngelaki A, Ashoor G, [et al.]. Noninvasive prenatal testing for fetal trisomies in a routinely screened first-trimester population. Am J Obstet Gynecol. 2012, 207, 374.e1-6.
-
(2012)
Am J Obstet Gynecol.
, vol.207
-
-
Nicolaides, K.1
Syngelaki, A.2
Ashoor, G.3
-
50
-
-
84871369642
-
The fetal fraction of cell-free DNA in maternal plasma is not affected by a priori risk of fetal trisomy
-
Brar H, Wang E, Struble C, [et al.]. The fetal fraction of cell-free DNA in maternal plasma is not affected by a priori risk of fetal trisomy. J Matern Fetal Neonatal Med. 2013, 26, 143-145.
-
(2013)
J Matern Fetal Neonatal Med.
, vol.26
, pp. 143-145
-
-
Brar, H.1
Wang, E.2
Struble, C.3
-
51
-
-
84871565053
-
Non-invasive prenatal testing for fetal aneuploidy: charting the course from clinical validity to clinical utility
-
Hui L. Non-invasive prenatal testing for fetal aneuploidy: charting the course from clinical validity to clinical utility. Ultrasound Obstet Gynecol. 2013, 41, 2-6.
-
(2013)
Ultrasound Obstet Gynecol.
, vol.41
, pp. 2-6
-
-
Hui, L.1
-
52
-
-
84866899806
-
Non-invasive prenatal diagnosis for Down syndrome: no paradigm shift, just better testing and it is already here!
-
Verweij E, de Boer M, Oepkes D. Non-invasive prenatal diagnosis for Down syndrome: no paradigm shift, just better testing and it is already here! Ultrasound Obstet Gynecol. 2012, 40, 484-485.
-
(2012)
Ultrasound Obstet Gynecol.
, vol.40
, pp. 484-485
-
-
Verweij, E.1
de Boer, M.2
Oepkes, D.3
-
53
-
-
84856328923
-
Non-invasive prenatal diagnosis for Down syndrome: the paradigm will shift, but slowly
-
Benn P, Cuckle H, Pergament E. Non-invasive prenatal diagnosis for Down syndrome: the paradigm will shift, but slowly. Ultrasound Obstet Gynecol. 2012, 39, 127-130.
-
(2012)
Ultrasound Obstet Gynecol.
, vol.39
, pp. 127-130
-
-
Benn, P.1
Cuckle, H.2
Pergament, E.3
-
54
-
-
67650258731
-
Fetal loss rate after chorionic villus sampling and amniocentesis: an 11-year national registry study
-
Tabor A, Vestergaard C, Lidegaard Ø. Fetal loss rate after chorionic villus sampling and amniocentesis: an 11-year national registry study. Ultrasound Obstet Gynecol. 2009, 34, 19-24.
-
(2009)
Ultrasound Obstet Gynecol.
, vol.34
, pp. 19-24
-
-
Tabor, A.1
Vestergaard, C.2
Lidegaard, Ø.3
-
55
-
-
85010357134
-
Analiza biopsji trofoblastu przeprowadzonych w I Klinice Ginekologii i Poloznictwa - CMKP SPSK im
-
Perinatologia, Neonatologia i Ginekologia
-
Bijok J, Szyszka M, Michalowska A, Roszkowski T[et al.]. Analiza biopsji trofoblastu przeprowadzonych w I Klinice Ginekologii i Poloznictwa - CMKP SPSK im. Prof. Orlowskiego w Warszawie - doniesienie wstepne. Perinatologia, Neonatologia i Ginekologia. 2010, 3, 145-152.
-
(2010)
Prof. Orlowskiego w Warszawie - doniesienie wstepne.
, vol.3
, pp. 145-152
-
-
Bijok, J.1
Szyszka, M.2
Michalowska, A.3
Roszkowski, T.4
-
56
-
-
0032731315
-
Clinical implications of atypical chromosome abnormalities diagnosed prenatally
-
Silver R, Blum K, Geibel L, [et al.]. Clinical implications of atypical chromosome abnormalities diagnosed prenatally. Obstet Gynecol. 1999, 94, 925-928.
-
(1999)
Obstet Gynecol.
, vol.94
, pp. 925-928
-
-
Silver, R.1
Blum, K.2
Geibel, L.3
-
57
-
-
85010350001
-
-
http://lifecodexx.com/yourcontactpersons0.html
-
-
-
-
58
-
-
84877926367
-
Noninvasive Prenatal Testing/Noninvasive Prenatal Diagnosis: the Position of the National Society of Genetic Counselors
-
Devers P, Cronister A, Ormond K, [et al.]. Noninvasive Prenatal Testing/Noninvasive Prenatal Diagnosis: the Position of the National Society of Genetic Counselors. J Genet Couns. 2013, 22, 291-295.
-
(2013)
J Genet Couns.
, vol.22
, pp. 291-295
-
-
Devers, P.1
Cronister, A.2
Ormond, K.3
-
59
-
-
84870156368
-
American College of Obstetricians and Gynecologists Committee on Genetics
-
Committee Opinion No 545: Noninvasive prenatal testing for fetal aneuploidy
-
American College of Obstetricians and Gynecologists Committee on Genetics. Committee Opinion No. 545: Noninvasive prenatal testing for fetal aneuploidy. Obstet Gynecol. 2012, 120, 1532-1534.
-
(2012)
Obstet Gynecol.
, vol.120
, pp. 1532-1534
-
-
|