-
1
-
-
0000901401
-
46,XY/47,XY,+ 17 mosaicism in a newborn with severe malformations
-
Bullerdiek, J., Bartnitzke, S. (1982). 46,XY/47,XY,+ 17 mosaicism in a newborn with severe malformations, Hum. Genet., 60, 296.
-
(1982)
Hum. Genet.
, vol.60
, pp. 296
-
-
Bullerdiek, J.1
Bartnitzke, S.2
-
2
-
-
0021915543
-
On the significance of true trisomy 20 mosaicism in amniotic fluid culture
-
Djalali, M., Steinbach, P., Schwinger, E., Schwanitz, G., Tettenborn, U., Wolf, M. (1985). On the significance of true trisomy 20 mosaicism in amniotic fluid culture, Hum. Genet., 69, 321-326.
-
(1985)
Hum. Genet.
, vol.69
, pp. 321-326
-
-
Djalali, M.1
Steinbach, P.2
Schwinger, E.3
Schwanitz, G.4
Tettenborn, U.5
Wolf, M.6
-
3
-
-
0025878403
-
Mosaic trisomy 17 in amniotic fluid cells not confirmed in the newborn
-
Djalali, M., Barbi, G., Grab, D. (1991). Mosaic trisomy 17 in amniotic fluid cells not confirmed in the newborn, Prenat. Diagn., 11, 399-402.
-
(1991)
Prenat. Diagn.
, vol.11
, pp. 399-402
-
-
Djalali, M.1
Barbi, G.2
Grab, D.3
-
4
-
-
0019198839
-
A cytogenetic study of 1000 spontaneous abortions
-
Hassold, T., Chen, N., Funkhouser, J., Joos, T., Manuel, B., Matsuura, J., Matsuyama, A., Wilson, C., Yamane, J.A., Jacobs, P.A. (1980). A cytogenetic study of 1000 spontaneous abortions, Ann. Hum. Genet., London, 44, 151-178.
-
(1980)
Ann. Hum. Genet., London
, vol.44
, pp. 151-178
-
-
Hassold, T.1
Chen, N.2
Funkhouser, J.3
Joos, T.4
Manuel, B.5
Matsuura, J.6
Matsuyama, A.7
Wilson, C.8
Yamane, J.A.9
Jacobs, P.A.10
-
5
-
-
0019995804
-
Mosaic trisomies in human spontaneous abortions
-
Hassold, T. (1982). Mosaic trisomies in human spontaneous abortions, Hum. Genet., 61, 31-35.
-
(1982)
Hum. Genet.
, vol.61
, pp. 31-35
-
-
Hassold, T.1
-
6
-
-
0025753402
-
A revisit of trisomy 20 mosaicism in prenatal diagnosis - An overview of 103 cases
-
Hsu, L.Y.F., Kaffe, S., Perlis, T.E. (1991). A revisit of trisomy 20 mosaicism in prenatal diagnosis - an overview of 103 cases, Prenat. Diagn., 11, 7-15.
-
(1991)
Prenat. Diagn.
, vol.11
, pp. 7-15
-
-
Hsu, L.Y.F.1
Kaffe, S.2
Perlis, T.E.3
-
7
-
-
0026741249
-
Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies
-
Hsu, L.Y.F., Kaffe, S., Jenkins, E.G., Alfonso, L., Benn, P.A., David, K., Hirschhorn, K., Lieber, E., Shanske, A., Shapiro, L.R., Schutta, E., Warburton, D. (1992). Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies, Prenat. Diagn., 12, 555-573.
-
(1992)
Prenat. Diagn.
, vol.12
, pp. 555-573
-
-
Hsu, L.Y.F.1
Kaffe, S.2
Jenkins, E.G.3
Alfonso, L.4
Benn, P.A.5
David, K.6
Hirschhorn, K.7
Lieber, E.8
Shanske, A.9
Shapiro, L.R.10
Schutta, E.11
Warburton, D.12
-
8
-
-
0030973681
-
Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20 and 21: Karyotype/phenotype correlations
-
Hsu, L.Y.F., Yu, M.-T., Neu, R.L., van Dyke, D.L., Benn, P.A., Bradshaw, C.L., Shaffer, L.G., Higgins, R.R., Khodr, G.S., Morton, C.C., Wang, H., Brothman, A.R., Chadwick, D., Disteche, C.M., Jenkins, L.S., Kalousek, D.K., Pantzar, T.J., Wyatt, P. (1997). Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20 and 21: karyotype/phenotype correlations, Prenat. Diagn., 17, 201-242.
-
(1997)
Prenat. Diagn.
, vol.17
, pp. 201-242
-
-
Hsu, L.Y.F.1
Yu, M.-T.2
Neu, R.L.3
Van Dyke, D.L.4
Benn, P.A.5
Bradshaw, C.L.6
Shaffer, L.G.7
Higgins, R.R.8
Khodr, G.S.9
Morton, C.C.10
Wang, H.11
Brothman, A.R.12
Chadwick, D.13
Disteche, C.M.14
Jenkins, L.S.15
Kalousek, D.K.16
Pantzar, T.J.17
Wyatt, P.18
-
9
-
-
0018887287
-
Anatomic and chromosomal anomalies in 639 spontaneous abortuses
-
Kajii, T., Ferrier, A., Niikawa, N., Takahara, H., Ohama, K., Avirachan, S. (1980). Anatomic and chromosomal anomalies in 639 spontaneous abortuses, Hum. Genet., 55, 87-98.
-
(1980)
Hum. Genet.
, vol.55
, pp. 87-98
-
-
Kajii, T.1
Ferrier, A.2
Niikawa, N.3
Takahara, H.4
Ohama, K.5
Avirachan, S.6
-
10
-
-
0023197381
-
Confined chorionic mosaicism in prenatal diagnosis
-
Kalousek, D.K., Dill, F.J., Pantzar, P., McGillivary, B.C., Yong, S.L., Wilson, R.D. (1987). Confined chorionic mosaicism in prenatal diagnosis, Hum. Genet., 77, 163-167.
-
(1987)
Hum. Genet.
, vol.77
, pp. 163-167
-
-
Kalousek, D.K.1
Dill, F.J.2
Pantzar, P.3
McGillivary, B.C.4
Yong, S.L.5
Wilson, R.D.6
-
11
-
-
0029162269
-
Uniparental disomy in humans: Development of an imprinting map and its implications for prenatal diagnosis
-
Ledbetter, D.H., Engel, E. (1995). Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis, Hum. Mol. Genet., 4, 1757-1764.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1757-1764
-
-
Ledbetter, D.H.1
Engel, E.2
-
12
-
-
0026770975
-
Canadian multicentre randomized clinical trial of chorion villus sampling and amniocentesis
-
Lippmann, A., Tomkins, D.J., Shime, J., Hamerton, J.L. (1992). Canadian multicentre randomized clinical trial of chorion villus sampling and amniocentesis, Prenat. Diagn., 12, 385-476.
-
(1992)
Prenat. Diagn.
, vol.12
, pp. 385-476
-
-
Lippmann, A.1
Tomkins, D.J.2
Shime, J.3
Hamerton, J.L.4
-
13
-
-
0024362374
-
Confirmation of prenatal diagnosis of sex chromosome mosaicism
-
McFadden, D.E., Kalousek, D.K. (1989). Confirmation of prenatal diagnosis of sex chromosome mosaicism, Am. J. Med. Genet., 32, 495-497.
-
(1989)
Am. J. Med. Genet.
, vol.32
, pp. 495-497
-
-
McFadden, D.E.1
Kalousek, D.K.2
-
14
-
-
0030033537
-
A clinical and molecular study of mosaicism for trisomy 17
-
Shaffer, L.G., McCaskill, Ch., Hersh, J.H., Greenberg, F., Lupski, J.R. (1996). A clinical and molecular study of mosaicism for trisomy 17, Hum. Genet., 97, 69-72.
-
(1996)
Hum. Genet.
, vol.97
, pp. 69-72
-
-
Shaffer, L.G.1
McCaskill, Ch.2
Hersh, J.H.3
Greenberg, F.4
Lupski, J.R.5
-
15
-
-
0025190806
-
Incidence and timing of pregnancy losses: Relevance to evaluating safety of early prenatal diagnosis
-
Simpson, J.L. (1990). Incidence and timing of pregnancy losses: relevance to evaluating safety of early prenatal diagnosis, Am. J. Med. Genet., 35, 165-173.
-
(1990)
Am. J. Med. Genet.
, vol.35
, pp. 165-173
-
-
Simpson, J.L.1
-
16
-
-
0026856030
-
Chromosome mosaicism in CVS and amniocentesis samples
-
Teshima, I.E., Kalousek, D.K., Vekemans, M.J.J., Markovic, V., Cox, D.M., Dallaire, L., Gagne, R., Lin, J.C.C., Ray, M., Sergovich, F.R., Uchida, I.A., Wang, H., Tomkins, D.J. (1992). Chromosome mosaicism in CVS and amniocentesis samples, Prenat. Diagn., 12, 443-446.
-
(1992)
Prenat. Diagn.
, vol.12
, pp. 443-446
-
-
Teshima, I.E.1
Kalousek, D.K.2
Vekemans, M.J.J.3
Markovic, V.4
Cox, D.M.5
Dallaire, L.6
Gagne, R.7
Lin, J.C.C.8
Ray, M.9
Sergovich, F.R.10
Uchida, I.A.11
Wang, H.12
Tomkins, D.J.13
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