-
1
-
-
84860213983
-
Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing
-
Bianchi DW, Platt LD, Goldberg JD, et al. Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing. Obstet Gynecol 2012;119:890-901.
-
(2012)
Obstet Gynecol
, vol.119
, pp. 890-901
-
-
Bianchi, D.W.1
Platt, L.D.2
Goldberg, J.D.3
-
2
-
-
80755172331
-
DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study
-
Palomaki GE, Kloza EM, Lambert-Messerlian GM, et al. DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study. Genet Med 2011;13:913-20.
-
(2011)
Genet Med
, vol.13
, pp. 913-920
-
-
Palomaki, G.E.1
Kloza, E.M.2
Lambert-Messerlian, G.M.3
-
3
-
-
84864408781
-
Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18
-
Norton ME, Brar H, Weiss J, et al. Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for 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.E.1
Brar, H.2
Weiss, J.3
-
4
-
-
84862776853
-
Prenatal Detection of Down Syndrome using Massively Parallel Sequencing (MPS): a rapid response statement from a committee on behalf of the Board of the International Society for Prenatal Diagnosis, 24 October 2011
-
Benn P, Borrell A, Cuckle H, et al. Prenatal Detection of Down Syndrome using Massively Parallel Sequencing (MPS): a rapid response statement from a committee on behalf of the Board of the International Society for Prenatal Diagnosis, 24 October 2011. Prenat Diagn 2012;32:1-2.
-
(2012)
Prenat Diagn
, vol.32
, pp. 1-2
-
-
Benn, P.1
Borrell, A.2
Cuckle, H.3
-
5
-
-
84878163766
-
-
Noninvasive prenatal testing/noninvasive prenatal diagnosis: the position of the National Society of Genetic Counselors (by NSGC Public Policy Committee). NSGC Position Statements .
-
Devers PL, Cronister A, Ormond KE, et al. Noninvasive prenatal testing/noninvasive prenatal diagnosis: the position of the National Society of Genetic Counselors (by NSGC Public Policy Committee). NSGC Position Statements 2012.
-
(2012)
-
-
Devers, P.L.1
Cronister, A.2
Ormond, K.E.3
-
6
-
-
84870156368
-
Committee Opinion No. 545: noninvasive prenatal testing for fetal aneuploidy
-
American College of Obstetricians and Gynecologists Committee on Genetics. . ;:-.
-
American College of Obstetricians and Gynecologists Committee on Genetics. Committee Opinion No. 545: noninvasive prenatal testing for fetal aneuploidy. Obstet Gynecol 2012;120:1532-4.
-
(2012)
Obstet Gynecol
, vol.120
, pp. 1532-1534
-
-
-
7
-
-
84878146092
-
Massively parallel sequencing of maternal plasma DNA in 113 cases of fetal nuchal cystic hygroma
-
DOI: 10.1097/AOG.0b013e31828ba3d8
-
Bianchi DW, Prosen T, Platt LD, et al. Massively parallel sequencing of maternal plasma DNA in 113 cases of fetal nuchal cystic hygroma. Obstet Gynecol 2013, DOI: 10.1097/AOG.0b013e31828ba3d8
-
(2013)
Obstet Gynecol
-
-
Bianchi, D.W.1
Prosen, T.2
Platt, L.D.3
-
8
-
-
84878159751
-
Discordant noninvasive prenatal testing results in a patient subsequently diagnosed with metastatic disease
-
Osborne CM, Hardisty E, Devers P, et al. Discordant noninvasive prenatal testing results in a patient subsequently diagnosed with metastatic disease. Prenat Diagn 2013;33:609-11.
-
(2013)
Prenat Diagn
, vol.33
, pp. 609-611
-
-
Osborne, C.M.1
Hardisty, E.2
Devers, P.3
-
9
-
-
0036644309
-
Clinical, cytogenetic, and molecular findings in 45,X/47,XX,+18 mosaicism: clinical report and review of the literature
-
Schubert R, Eggermann T, Hofstaetter C, et al. Clinical, cytogenetic, and molecular findings in 45, X/47, XX, +18 mosaicism: clinical report and review of the literature. Am J Med Genet 2002;110:278-82.
-
(2002)
Am J Med Genet
, vol.110
, pp. 278-282
-
-
Schubert, R.1
Eggermann, T.2
Hofstaetter, C.3
-
11
-
-
3042831726
-
Chromosome abnormalities identified in 347 spontaneous abortions collected in Japan
-
Nagaishi M, Yamamoto T, Iinuma K, et al. Chromosome abnormalities identified in 347 spontaneous abortions collected in Japan. J Obstet Gynaecol Res 2004;30:237-41.
-
(2004)
J Obstet Gynaecol Res
, vol.30
, pp. 237-241
-
-
Nagaishi, M.1
Yamamoto, T.2
Iinuma, K.3
-
12
-
-
84857868297
-
DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study
-
Palomaki GE, Deciu C, Kloza EM, et al. DNA sequencing of maternal plasma reliably identifies 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.E.1
Deciu, C.2
Kloza, E.M.3
-
13
-
-
84870688045
-
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;32:1225-32.
-
(2012)
Prenat Diagn
, vol.32
, pp. 1225-1232
-
-
Dan, S.1
Wang, W.2
Ren, J.3
-
14
-
-
33845942655
-
ACOG Practice Bulletin No. 77: screening for fetal chromosomal abnormalities
-
ACOG Committee on Practice Bulletin. . ;:-.
-
ACOG Committee on Practice Bulletin. ACOG Practice Bulletin No. 77: screening for fetal chromosomal abnormalities. Obstet Gynecol 2007;109:217-27.
-
(2007)
Obstet Gynecol
, vol.109
, pp. 217-227
-
-
-
15
-
-
84876270082
-
Noninvasive prenatal testing for fetal aneuploidy
-
Norton ME, Rose NC, Benn P. Noninvasive prenatal testing for fetal aneuploidy. Obstet Gynecol 2013;121:847-50.
-
(2013)
Obstet Gynecol
, vol.121
, pp. 847-850
-
-
Norton, M.E.1
Rose, N.C.2
Benn, P.3
-
16
-
-
84874510427
-
The impact of utilization of early aneuploidy screening on amniocenteses available for training in obstetrics and fetal medicine
-
Rose NC, Lagrave D, Hafen B, et al. The impact of utilization of early aneuploidy screening on amniocenteses available for training in obstetrics and fetal medicine. Prenat Diagn 2013;33:242-4.
-
(2013)
Prenat Diagn
, vol.33
, pp. 242-244
-
-
Rose, N.C.1
Lagrave, D.2
Hafen, B.3
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