-
1
-
-
84894895574
-
Clinical results on single cells from 470 embyros using 23-chromosome single nucleotide polymorphism (SNP) microarray preimplanta-tion genetic screening (PGS) from 45 patients
-
Benner, A., Chipko, C., Pen, R. and Kearns, W.G. (2010) Clinical results on single cells from 470 embyros using 23-chromosome single nucleotide polymorphism (SNP) microarray preimplanta-tion genetic screening (PGS) from 45 patients. Fertil Steril 94:S123.
-
(2010)
Fertil Steril
, vol.94
-
-
Benner, A.1
Chipko, C.2
Pen, R.3
Kearns, W.G.4
-
2
-
-
51349150718
-
Chromosomal abnormalities in miscarriages after different assisted reproduction procedures
-
Bettio, D., Venci, A. and Levi Setti, P.E. (2008) Chromosomal abnormalities in miscarriages after different assisted reproduction procedures. Placenta 29: pSB126-S128.
-
(2008)
Placenta
, vol.29
-
-
Bettio, D.1
Venci, A.2
Levi Setti, P.E.3
-
3
-
-
35348965707
-
From microscopes to microarrays: Dissecting recurrent chromosomal rearrangements
-
Emanuel, B.S and Saitta, S.C. (2007) From microscopes to microar-rays: dissecting recurrent chromosomal rearrangements. Nat Rev Genet 8:p869-883.
-
(2007)
Nat Rev Genet
, vol.8
, pp. 869-883
-
-
Emanuel, B.S.1
Saitta, S.C.2
-
4
-
-
34547460100
-
Pregnancy loss among pregnancies conceived through assisted reproductive technology, United States, 1999-2002
-
Farr, S.L., Schieve, L.A. and Jamieson, D.J. (2007) Pregnancy loss among pregnancies conceived through assisted reproductive technology, United States, 1999-2002. Am J Epidemiol 165:1380-1388.
-
(2007)
Am J Epidemiol
, vol.165
, pp. 1380-1388
-
-
Farr, S.L.1
Schieve, L.A.2
Jamieson, D.J.3
-
5
-
-
78049346960
-
Chromosomal abnormalities in spontaneous abortion after assisted reproductive treatment
-
Kim, J.W., Lee,W.S., Yoon, T.K., Seok, H.H., Cho, J.H., Kim, Y.S.et al. , (2010) Chromosomal abnormalities in spontaneous abortion after assisted reproductive treatment. BMC Medical Genetics 11:153.
-
(2010)
BMC Medical Genetics
, vol.11
, pp. 153
-
-
Kim, J.W.1
Lee, W.S.2
Yoon, T.K.3
Seok, H.H.4
Cho, J.H.5
Kim, Y.S.6
-
6
-
-
84863279486
-
Informatics enhanced SNP microarray analysis of 30 miscarriage samples compared to routine cytoge-netics
-
Lathi, R.B., Massie, J.A., Loring, M., Demko, Z.P., Johnson, D., Sigurjonsson, S., et al. (2012) Informatics enhanced SNP microarray analysis of 30 miscarriage samples compared to routine cytoge-netics. PLoS One 7:e31282.
-
(2012)
PLoS One
, vol.7
-
-
Lathi, R.B.1
Massie, J.A.2
Loring, M.3
Demko, Z.P.4
Johnson, D.5
Sigurjonsson, S.6
-
7
-
-
21344459794
-
Genetic evaluation and counseling of couples with recurrent miscarriage: Recommendations of the National Society of Genetic Counselors
-
Laurino, M.Y., Bennett, R.L., Saraiya, D.S., Baumeister, L., Doyle, D.L., Leppig, K., et al. (2005) Genetic evaluation and counseling of couples with recurrent miscarriage: recommendations of the National Society of Genetic Counselors. J Genet Couns 14:165-181.
-
(2005)
J Genet Couns
, vol.14
, pp. 165-181
-
-
Laurino, M.Y.1
Bennett, R.L.2
Saraiya, D.S.3
Baumeister, L.4
Doyle, D.L.5
Leppig, K.6
-
8
-
-
77952032690
-
Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies
-
Miller, D.T, Adam, M.P., Aradhya, S., Biesecker, L.G., Brothman, A.R., Carter, N.P., et al., (2010) Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies. Am J Hum Genet 86:749-764.
-
(2010)
Am J Hum Genet
, vol.86
, pp. 749-764
-
-
Miller, D.T.1
Adam, M.P.2
Aradhya, S.3
Biesecker, L.G.4
Brothman, A.R.5
Carter, N.P.6
-
9
-
-
0034709737
-
Maternal age and fetal loss: Population based register linkage study
-
Nybo Andersen, A.M., Wohlfahrt, J., Christens, P., Olsen, J. and Melbye, M. (2000) Maternal age and fetal loss: population based register linkage study. BMJ 320:p1708-1712.
-
(2000)
BMJ
, vol.320
-
-
Nybo Andersen, A.M.1
Wohlfahrt, J.2
Christens, P.3
Olsen, J.4
Melbye, M.5
-
10
-
-
2442666390
-
Comparative Genomic Hybridization - Array Analysis Enhances the Detection of Aneuploidies and Submicroscopic Imbalances in Spontaneous Miscarriages
-
Schaeffer, A.J., Chung, J., Heretis, K., Wong, A., Ledbetter, D.H. and Lese Martin, C. (2004) Comparative Genomic Hybridization - Array Analysis Enhances the Detection of Aneuploidies and Submicroscopic Imbalances in Spontaneous Miscarriages. Am. J. Hum. Genet 74:1168-1174.
-
(2004)
Am. J. Hum. Genet
, vol.74
, pp. 1168-1174
-
-
Schaeffer, A.J.1
Chung, J.2
Heretis, K.3
Wong, A.4
Ledbetter, D.H.5
Lese Martin, C.6
-
11
-
-
77952092573
-
Recurrent miscarriage: Current concepts in diagnosis and treatment
-
Toth, B., Jeschke, U., Rogenhofer, N., Scholz, C., Würfel, W., Thaler, C.J., et al. (2010) Recurrent miscarriage: current concepts in diagnosis and treatment. J Reprod Immunol 85:25-32.
-
(2010)
J Reprod Immunol
, vol.85
, pp. 25-32
-
-
Toth, B.1
Jeschke, U.2
Rogenhofer, N.3
Scholz, C.4
Würfel, W.5
Thaler, C.J.6
-
12
-
-
79952987085
-
Single nucleotide polymorphism microarray-based concurrent screening of 24-chromosome aneuploidy and unbalanced translocations in preimplantation human embryos
-
e1-2
-
Treff, N.R., Northrop, L.E., Kasabwala, K., Su, J., Levy, B. and Scott, R. T. (2011) Single nucleotide polymorphism microarray-based concurrent screening of 24-chromosome aneuploidy and unbalanced translocations in preimplantation human embryos. Fertil Steril 95:1606-12.e1-2.
-
(2011)
Fertil Steril
, vol.95
, pp. 1606-12
-
-
Treff, N.R.1
Northrop, L.E.2
Kasabwala, K.3
Su, J.4
Levy, B.5
Scott, R.T.6
-
13
-
-
79951959735
-
Array technology in prenatal diagnosis
-
Zuffardi, O., Vetro, A., Brady, P. and Vermeesch, J. (2011) Array technology in prenatal diagnosis. Semin Fetal Neonatal Med 16:94-98.
-
(2011)
Semin Fetal Neonatal Med
, vol.16
, pp. 94-98
-
-
Zuffardi, O.1
Vetro, A.2
Brady, P.3
Vermeesch, J.4
-
14
-
-
80155173615
-
Chromosome karyotyping of 220 cases of early spontaneous abortion
-
Gu, Y., Xie, J. S., Luo, F.-W., Geng, X., Zhang, H.-K., Shen, H.-N., et al. (2009) Chromosome karyotyping of 220 cases of early spontaneous abortion. Chinese Journal of Birth Health and Heredity 17:38-39.
-
(2009)
Chinese Journal of Birth Health and Heredity
, vol.17
, pp. 38-39
-
-
Gu, Y.1
Xie, J.S.2
Luo, F.-W.3
Geng, X.4
Zhang, H.-K.5
Shen, H.-N.6
|