-
1
-
-
0032517538
-
6-Year experience of prenatal diagnosis in an unselected population in Oxford, UK
-
BOYD P. A., CHAMBERLAIN P, HICKS N.R.: 6-year experience of prenatal diagnosis in an unselected population in Oxford, UK. Lancet, 1998, 352, 1577-1581.
-
(1998)
Lancet
, vol.352
, pp. 1577-1581
-
-
Boyd, P.A.1
Chamberlain, P.2
Hicks, N.R.3
-
2
-
-
0033555450
-
Frequencies of chromosomal abnormalities at amniocentesis: Over 20 years of cytogenetic analyses in one laboratory
-
CARON L., TIHY F, DALLAIRE L.: Frequencies of chromosomal abnormalities at amniocentesis: over 20 years of cytogenetic analyses in one laboratory. Am. J. Med. Genet., 1999, 82, 149-154.
-
(1999)
Am. J. Med. Genet.
, vol.82
, pp. 149-154
-
-
Caron, L.1
Tihy, F.2
Dallaire, L.3
-
3
-
-
0034850494
-
Prenatal diagnosis of chromosome disorders in Tunisian population
-
CHAABOUNI H., CHAABOUNI M., MAAZOUL F., M'RAD R., BEN JEMAA L., SMAOUI N., TERRAS K., KAMMOUN H., BELGHITH N., RIDENE H., BOUJEMAA O., ZOUARI F.: Prenatal diagnosis of chromosome disorders in Tunisian population. Ann. Genet., 2001, 44, 99-104.
-
(2001)
Ann. Genet.
, vol.44
, pp. 99-104
-
-
Chaabouni, H.1
Chaabouni, M.2
Maazoul, F.3
M'rad, R.4
Ben Jemaa, L.5
Smaoui, N.6
Terras, K.7
Kammoun, H.8
Belghith, N.9
Ridene, H.10
Boujemaa, O.11
Zouari, F.12
-
4
-
-
1642471074
-
Evaluation of 437 amniotic fluid samples in prenatal diagnosis
-
COGULU O., TAS M.A., BOZOKLAR R., OZKINAY F.: Evaluation of 437 amniotic fluid samples in prenatal diagnosis. J. Neonatology. 1998, 5, 25-29.
-
(1998)
J. Neonatology
, vol.5
, pp. 25-29
-
-
Cogulu, O.1
Tas, M.A.2
Bozoklar, R.3
Ozkinay, F.4
-
5
-
-
0017726811
-
Prenatal diagnosis of genetic diseases
-
EPSTEIN C.J., GOLBUS M.S.: Prenatal diagnosis of genetic diseases. Am. Sci., 1977, 65, 703-711.
-
(1977)
Am. Sci.
, vol.65
, pp. 703-711
-
-
Epstein, C.J.1
Golbus, M.S.2
-
6
-
-
0015025592
-
Amniocentesis in genetic counselling
-
GERBIE A.B., NADLER H.L., GERBIE M. V.: Amniocentesis in genetic counselling. Am. J. Obstet. Gynecol., 1971, 109, 765-768.
-
(1971)
Am. J. Obstet. Gynecol.
, vol.109
, pp. 765-768
-
-
Gerbie, A.B.1
Nadler, H.L.2
Gerbie, M.V.3
-
7
-
-
0027174623
-
Genetic amniocentesis: A six-years experience in an isolated region of northeastern Quebec (Canada)
-
HAMEL G., SIMARD L., GAGNE R., DE BRAEKELEER M.: Genetic amniocentesis: a six-years experience in an isolated region of northeastern Quebec (Canada). Genet. Counsel., 1993, 4, 103-108.
-
(1993)
Genet. Counsel.
, vol.4
, pp. 103-108
-
-
Hamel, G.1
Simard, L.2
Gagne, R.3
De Braekeleer, M.4
-
8
-
-
0020696212
-
Chromosomal abnormality rates at amniocentesis and in live-born infants
-
HOOK E.B., CROSS P.K., SCHREINEMACHERS D.M.: Chromosomal abnormality rates at amniocentesis and in live-born infants. JAMA, 1983, 249, 2034-2038.
-
(1983)
JAMA
, vol.249
, pp. 2034-2038
-
-
Hook, E.B.1
Cross, P.K.2
Schreinemachers, D.M.3
-
9
-
-
0026823361
-
Prenatal cytogenetic diagnosis in amniocentesis
-
HSIEH F.J., KO T.M., TSENG L.H., CHANG L.S., PAN M.F., CHUANG S.M., LEE T.Y., CHEN H.Y.: Prenatal cytogenetic diagnosis in amniocentesis. J. Formos. Med. Assoc., 1992, 91, 276-282.
-
(1992)
J. Formos. Med. Assoc.
, vol.91
, pp. 276-282
-
-
Hsieh, F.J.1
Ko, T.M.2
Tseng, L.H.3
Chang, L.S.4
Pan, M.F.5
Chuang, S.M.6
Lee, T.Y.7
Chen, H.Y.8
-
11
-
-
0016713786
-
A clinical service for prenatal diagnosis
-
LAXOVA R., LEWIS B. V., SUDDABY M.: A clinical service for prenatal diagnosis. Lancet, 1975, 2, 964-966.
-
(1975)
Lancet
, vol.2
, pp. 964-966
-
-
Laxova, R.1
Lewis, B.V.2
Suddaby, M.3
-
12
-
-
0026770975
-
Canadian multicentre randomized clinical trial of chorion villus sampling and amniocentesis
-
LIPPMAN A., TOMKINS D.J., SHIME J., HAMERTON J.L.: Canadian multicentre randomized clinical trial of chorion villus sampling and amniocentesis. Prenat. Diagn., 1992, 12, 385-476.
-
(1992)
Prenat. Diagn.
, vol.12
, pp. 385-476
-
-
Lippman, A.1
Tomkins, D.J.2
Shime, J.3
Hamerton, J.L.4
-
13
-
-
0342828784
-
Amniocentesis
-
D.J.H. Brock, C.H. Rodeck, M.A. Ferguson-Smith (eds). Hong Kong, Churchill Livingstone
-
MAC LACHLAN N.A.: Amniocentesis. In: Prenatal Diagnosis and Screening. D.J.H. Brock, C.H. Rodeck, M.A. Ferguson-Smith (eds). Hong Kong, Churchill Livingstone. 1992, 13-21.
-
(1992)
Prenatal Diagnosis and Screening
, pp. 13-21
-
-
Mac Lachlan, N.A.1
-
14
-
-
0025665386
-
Prenatal diagnosis of chromosome abnormalities
-
MURER-ORLANDO M., ZAHED L., DOCHERTY Z.: Prenatal diagnosis of chromosome abnormalities. Genetica, 1990, 83, 61-65.
-
(1990)
Genetica
, vol.83
, pp. 61-65
-
-
Murer-Orlando, M.1
Zahed, L.2
Docherty, Z.3
-
15
-
-
0032480524
-
Trends in prenatal screening for and diagnosis of Down's syndrome, England and Wales, 1989-97
-
MUTTON D., IDE R.G., ALBERMAN E.: Trends in prenatal screening for and diagnosis of Down's syndrome, England and Wales, 1989-97. BMJ, 1998, 317, 922-923.
-
(1998)
BMJ
, vol.317
, pp. 922-923
-
-
Mutton, D.1
Ide, R.G.2
Alberman, E.3
-
16
-
-
0023086246
-
Temporal changes in Ohio amniocentesis utilization during the first twelve years (1972-1983), and frequency of chromosome abnormalities observed
-
NABER J.M., HUETHER C.A., GOODWIN B.A.: Temporal changes in Ohio amniocentesis utilization during the first twelve years (1972-1983), and frequency of chromosome abnormalities observed. Prenat. Diagn., 1987, 7, 51-65.
-
(1987)
Prenat. Diagn.
, vol.7
, pp. 51-65
-
-
Naber, J.M.1
Huether, C.A.2
Goodwin, B.A.3
-
17
-
-
0031467063
-
Trends in the use of prenatal diagnosis in New York State and the impact of biochemical screening on the detection of Down syndrome, 1984-1993
-
OLSEN C.L., CROSS P.K.: Trends in the use of prenatal diagnosis in New York State and the impact of biochemical screening on the detection of Down syndrome, 1984-1993. Prenat. Diagn., 1997, 17, 1113-1124.
-
(1997)
Prenat. Diagn.
, vol.17
, pp. 1113-1124
-
-
Olsen, C.L.1
Cross, P.K.2
-
18
-
-
0036167673
-
A negative second trimester triple test and absence of specific ultrasonographic markers may decrease the need for genetic amniocentesis in advanced maternal age by 60%
-
ROSEN D.J., KEDAR I., AMIEL A., BEN-TOVIM T., PETEL Y., KANETI H., TOHAR M., FEJGIN M.D.: A negative second trimester triple test and absence of specific ultrasonographic markers may decrease the need for genetic amniocentesis in advanced maternal age by 60%. Prenat. Diagn., 2002, 22, 59-63.
-
(2002)
Prenat. Diagn.
, vol.22
, pp. 59-63
-
-
Rosen, D.J.1
Kedar, I.2
Amiel, A.3
Ben-Tovim, T.4
Petel, Y.5
Kaneti, H.6
Tohar, M.7
Fejgin, M.D.8
-
19
-
-
0034569316
-
Prenatal diagnosis, 10-year experience
-
SIRIVATANAPA P., TONGSONG T., WANAPIRAK C., SIRICHOTIYAKUL S., CHANPRAPAPH P., YAMPOCHAI A., TAKAPIITRA A., SEKARARITHI R.: Prenatal diagnosis, 10-year experience. J. Med. Assoc. Thai., 2000, 83, 1502-1528.
-
(2000)
J. Med. Assoc. Thai.
, vol.83
, pp. 1502-1528
-
-
Sirivatanapa, P.1
Tongsong, T.2
Wanapirak, C.3
Sirichotiyakul, S.4
Chanprapaph, P.5
Yampochai, A.6
Takapiitra, A.7
Sekararithi, R.8
-
20
-
-
0014021719
-
Chromosome analysis of human fluid cells
-
STEELE M.W., BREG W.R.: Chromosome analysis of human fluid cells. Lancet, 1966, 1, 383-385.
-
(1966)
Lancet
, vol.1
, pp. 383-385
-
-
Steele, M.W.1
Breg, W.R.2
-
21
-
-
0028716799
-
Prenatal diagnosis in Canada-1990. A review
-
STRANC L.C., EVANS J.A., HAMERTON J.L.: Prenatal diagnosis in Canada-1990. A review. Prenat. Diagn., 1994, 14, 1253-1255.
-
(1994)
Prenat. Diagn.
, vol.14
, pp. 1253-1255
-
-
Stranc, L.C.1
Evans, J.A.2
Hamerton, J.L.3
-
22
-
-
0029562541
-
Early amniocentesis. A clinical review
-
WILSON R.D.: Early amniocentesis, A clinical review. Prenat. Diagn., 1995, 15, 1259-1273.
-
(1995)
Prenat. Diagn.
, vol.15
, pp. 1259-1273
-
-
Wilson, R.D.1
-
23
-
-
0033203060
-
The Korean collaborative study on 11 000 prenatal genetic amniocentesis
-
YANG Y.H., JU K.S., KIM S.B., CHO Y.H., LEE J.H., LEE S.H., CHOI O.H., CHUN J.H., KIM J.I., KIM H.J., SOHN Y.S.: The Korean collaborative study on 11 000 prenatal genetic amniocentesis. Yonsei Med. J., 1999, 40, 460-466.
-
(1999)
Yonsei Med. J.
, vol.40
, pp. 460-466
-
-
Yang, Y.H.1
Ju, K.S.2
Kim, S.B.3
Cho, Y.H.4
Lee, J.H.5
Lee, S.H.6
Choi, O.H.7
Chun, J.H.8
Kim, J.I.9
Kim, H.J.10
Sohn, Y.S.11
-
24
-
-
0025878982
-
Single-center comparison of results of 1000 prenatal diagnoses with chorionic villus sampling and 1000 diagnoses with amniocentesis
-
YOUNG S.R., SHIPLEY C.F., WADE R.V., EDWARDS J.G., WATERS M.B., CANTU M.L., BEST R.G., DENIS E.J.: Single-center comparison of results of 1000 prenatal diagnoses with chorionic villus sampling and 1000 diagnoses with amniocentesis. Am. J. Obstet. Gynecol., 1991, 165, 255-263.
-
(1991)
Am. J. Obstet. Gynecol.
, vol.165
, pp. 255-263
-
-
Young, S.R.1
Shipley, C.F.2
Wade, R.V.3
Edwards, J.G.4
Waters, M.B.5
Cantu, M.L.6
Best, R.G.7
Denis, E.J.8
|