-
1
-
-
0020308904
-
Minor chromosomal variants and major chromosomal anomalies in couples with recurrent abortion
-
BLUMBERG B.D., SHULKIN J.D., ROTTER J.I., MOHANDAS T., KABACK M.M.: Minor chromosomal variants and major chromosomal anomalies in couples with recurrent abortion. Am. J. Hum. Genet., 1982, 43, 948-960.
-
(1982)
Am. J. Hum. Genet.
, vol.43
, pp. 948-960
-
-
Blumberg, B.D.1
Shulkin, J.D.2
Rotter, J.I.3
Mohandas, T.4
Kaback, M.M.5
-
2
-
-
0027527210
-
A prospective trial of prenatal screening for Down syndrome by means of maternal serum α-fetoprotein, human chronic gonadotropin, and unconjugated estriol
-
BURTON B.K., PRINS G.S., VERP M.S.: A prospective trial of prenatal screening for Down syndrome by means of maternal serum α-fetoprotein, human chronic gonadotropin, and unconjugated estriol. Am. J. Obstet. Gynecol., 1993, 169, 526-530.
-
(1993)
Am. J. Obstet. Gynecol.
, vol.169
, pp. 526-530
-
-
Burton, B.K.1
Prins, G.S.2
Verp, M.S.3
-
3
-
-
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
-
4
-
-
0034850494
-
Prenatal diagnosis of chromosome disorders in Tunisian population
-
CHAABOUNI H., CHAABOUNI M., MAAZOUL F., M'RAD R., JEMAA L.B., SMAOUI N., TERRAS K., KAMMOUN H., BELGHITH N., RIDENE H., OUESLATI B., ZOUARI.: 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
Jemaa, L.B.5
Smaoui, N.6
Terras, K.7
Kammoun, H.8
Belghith, N.9
Ridene, H.10
Oueslati, B.11
Zouari12
-
5
-
-
0027398092
-
A prospective evaluation of a second-trimester screening test for fetal Down syndrome using maternal serum alpha-fetoprotein, hCG, and unconjugated estriol
-
CHENG E.Y., LUTHY D.A., ZEBELMAN A.M., WlLLIAMS M.A., LIEPPMAN R.E., HICKOK D.E.: A prospective evaluation of a second-trimester screening test for fetal Down syndrome using maternal serum alpha-fetoprotein, hCG, and unconjugated estriol. Obstet. Gynecol., 1993, 81, 72-76.
-
(1993)
Obstet. Gynecol.
, vol.81
, pp. 72-76
-
-
Cheng, E.Y.1
Luthy, D.A.2
Zebelman, A.M.3
Wllliams, M.A.4
Lieppman, R.E.5
Hickok, D.E.6
-
6
-
-
0018939976
-
Chromosome findings in 2,500 second trimester amniocenteses
-
CRANDALL B.F., LEHGERZ T.B., RUBINSTEIN L., ROBERTSON R.D., SAMPLE W.F., SARTI D., HOWARD J.: Chromosome findings in 2,500 second trimester amniocenteses. Am. J. Med. Genet., 1980, 5, 345-356.
-
(1980)
Am. J. Med. Genet.
, vol.5
, pp. 345-356
-
-
Crandall, B.F.1
Lehgerz, T.B.2
Rubinstein, L.3
Robertson, R.D.4
Sample, W.F.5
Sarti, D.6
Howard, J.7
-
7
-
-
0020535881
-
Midtrimester amniocentesis; an analysis of 923 cases with neonatal follow-up
-
CRUIKSHANK D.P., VARNER M.W., CRUIKSHANK J.E., GRANT S.S., DONNELLY E.: Midtrimester amniocentesis; an analysis of 923 cases with neonatal follow-up. Am. J. Obstet. Gynecol., 1983, 146, 204-210.
-
(1983)
Am. J. Obstet. Gynecol.
, vol.146
, pp. 204-210
-
-
Cruikshank, D.P.1
Varner, M.W.2
Cruikshank, J.E.3
Grant, S.S.4
Donnelly, E.5
-
8
-
-
0020082173
-
Prenatal diagnosis in 3.000 women for chromosome, X-linked, and metabolic disorders
-
DANIEL A., STEWART L., SAVILLE T., BROKKWELL R., PAULL H., PURVIS-SMTH S., LAM-PO-TAMG P.R.L.C.: Prenatal diagnosis in 3.000 women for chromosome, X-linked, and metabolic disorders. Am. J. Med. Genet., 1982, 11, 61-75.
-
(1982)
Am. J. Med. Genet.
, vol.11
, pp. 61-75
-
-
Daniel, A.1
Stewart, L.2
Saville, T.3
Brokkwell, R.4
Paull, H.5
Purvis-Smth, S.6
Lam-Po-Tamg, P.R.L.C.7
-
9
-
-
0023264259
-
Effects of amniocentesis for genetic purpose on the pregnancy and its outcome
-
DAVIDSON E.V., MCINTOSH A.S., ROBERTS D.F.: Effects of amniocentesis for genetic purpose on the pregnancy and its outcome. J. Biosoc. Sci., 1987, 19, 295-304.
-
(1987)
J. Biosoc. Sci.
, vol.19
, pp. 295-304
-
-
Davidson, E.V.1
Mcintosh, A.S.2
Roberts, D.F.3
-
10
-
-
0036778110
-
Clinical procedures in prenatal diagnosis
-
EISENBERG B., WAPNER R.J.: Clinical procedures in prenatal diagnosis. Best. Pract. Res. Cl. Ob., 2002, 16(5), 611-627.
-
(2002)
Best. Pract. Res. Cl. Ob.
, vol.16
, Issue.5
, pp. 611-627
-
-
Eisenberg, B.1
Wapner, R.J.2
-
11
-
-
0024574028
-
Chromosomal prenatal diaposis: Study of 936 cases of intrauterine abnormalities after ultrasound assessment
-
EYDOUX P., CHOISET A., LE PORRIER N., THEPOT F., SZPIRO-TAPIA S., ALLIET J., RAMOND S., VIEL J.F., GAUTIER E., MORICHON N., GIRARD-ORGEOLET S:. Chromosomal prenatal diaposis: study of 936 cases of intrauterine abnormalities after ultrasound assessment. Prenat. Diagn., 1989, 9, 255-268.
-
(1989)
Prenat. Diagn.
, vol.9
, pp. 255-268
-
-
Eydoux, P.1
Choiset, A.2
Le Porrier, N.3
Thepot, F.4
Szpiro-Tapia, S.5
Alliet, J.6
Ramond, S.7
Viel, J.F.8
Gautier, E.9
Morichon, N.10
Girard-Orgeolet, S.11
-
12
-
-
0021045144
-
Amniotic fluid cell types and culture
-
GOSDEN C.M.: Amniotic fluid cell types and culture. Br. Med. Bull., 1983, 39, 348-354.
-
(1983)
Br. Med. Bull.
, vol.39
, pp. 348-354
-
-
Gosden, C.M.1
-
13
-
-
12144289745
-
Trends in cytogenetic prenatal diagnosis in a reference hospital in Izmir/Turkey: A comparative study for four years
-
GUNDUZ C., COGULU O., CANKAYA T., BORA E., KARACA E., ALPMANA, SAGOL S., ONAY H., OZKINAY Y., OZKINAY C.: Trends in cytogenetic prenatal diagnosis in a reference hospital in Izmir/Turkey: a comparative study for four years. Genet. Couns., 2004, 15(1), 53-59.
-
(2004)
Genet. Couns.
, vol.15
, Issue.1
, pp. 53-59
-
-
Gunduz, C.1
Cogulu, O.2
Cankaya, T.3
Bora, E.4
Karaca, E.5
Alpman, A.6
Sagol, S.7
Onay, H.8
Ozkinay, Y.9
Ozkinay, C.10
-
14
-
-
0027174623
-
Genetic amniocentesis: A six-year experience in an isolated region of northeastern Quebec (Canada)
-
HAMEL G., SIMARD L., GAGNE R., DE BRAEKELER M.: Genetic amniocentesis: a six-year experience in an isolated region of northeastern Quebec (Canada). Genet. Couns., 1993, 4(2), 103-108.
-
(1993)
Genet. Couns.
, vol.4
, Issue.2
, pp. 103-108
-
-
Hamel, G.1
Simard, L.2
Gagne, R.3
De Braekeler, M.4
-
15
-
-
0028006245
-
Indications and methods for antenatal chromosome analysis: More choices require more appropriate selection
-
HOLZGREVE W., GANSHIRT-AHLERT D., MINY P.: Indications and methods for antenatal chromosome analysis: more choices require more appropriate selection. Cur. Opin. Obstet. Gynecol., 1994, 6, 3-6.
-
(1994)
Cur. Opin. Obstet. Gynecol.
, vol.6
, pp. 3-6
-
-
Holzgreve, W.1
Ganshirt-Ahlert, D.2
Miny, P.3
-
16
-
-
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(3), 276-282.
-
(1992)
J. Formos. Med. Assoc.
, vol.91
, Issue.3
, 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
-
17
-
-
10544226872
-
Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and II
-
LAMB N.E., FREEMAN S.B., SAVAGE-AUSTIN A., PETTAY D., TAFT L., HERSEY J., GU Y., SHEN J., SAKER D., MAY K.M., AVRAMOPOULOS D., PETERSEN M.B., HALLBERG A., MIKKELSEN M., HASSOLD T.J., SHERMAN S.L.: Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and II. Nat. Genet., 1996, 14, 400-405.
-
(1996)
Nat. Genet.
, vol.14
, pp. 400-405
-
-
Lamb, N.E.1
Freeman, S.B.2
Savage-Austin, A.3
Pettay, D.4
Taft, L.5
Hersey, J.6
Gu, Y.7
Shen, J.8
Saker, D.9
May, K.M.10
Avramopoulos, D.11
Petersen, M.B.12
Hallberg, A.13
Mikkelsen, M.14
Hassold, T.J.15
Sherman, S.L.16
-
18
-
-
0026698901
-
Prenatal cytogenetic diagnosis of 1,400 consecutive amniocenteses
-
MATHEWS T., NAVSARIA D., VERMA.: Prenatal cytogenetic diagnosis of 1,400 consecutive amniocenteses. Gynecol. Obstet. Invest., 1992, 34, 122-123.
-
(1992)
Gynecol. Obstet. Invest.
, vol.34
, pp. 122-123
-
-
Mathews, T.1
Navsaria, D.2
Verma3
-
19
-
-
4344610162
-
Genetic amniocentesis complications: Is the incidence overrated?
-
NASSAR A.H., MARTIN D., GONZALEZ-QUINTERO V.H., GOMEZ-MARIN O., GUTIERREZ A., O'SULLIVAN M.J.: Genetic amniocentesis complications: is the incidence overrated? Gynecol. Obstet. Invest., 2004, 58(2), 100-104.
-
(2004)
Gynecol. Obstet. Invest.
, vol.58
, Issue.2
, pp. 100-104
-
-
Nassar, A.H.1
Martin, D.2
Gonzalez-Quintero, V.H.3
Gomez-Marin, O.4
Gutierrez, A.5
O'Sullivan, M.J.6
-
20
-
-
0015246254
-
A rapid banding technique for human chromosomes
-
SEABRIGHT M.: A rapid banding technique for human chromosomes. Lancet, 1971, 2(7731), 971-972.
-
(1971)
Lancet
, vol.2
, Issue.7731
, pp. 971-972
-
-
Seabright, M.1
-
21
-
-
0026000975
-
Trisomy 21: Association between reduced recombination and nondisjunction
-
SHERMAN S.L., TAKAESU N., FREEMAN S.B., GRANTHAM M., PHILLIPS C., BLACKSTON R.D., JACOBS P.A., COCK WELL A.E., FREEMAN V., UCHIDA I., MKKELSEN M., KURNIT D.M., BURACZYNSKA M., KEATS B.J.B., HASSOLD T.J.: Trisomy 21: Association between reduced recombination and nondisjunction. Am. J. Hum. Genet., 1991, 49, 608-620.
-
(1991)
Am. J. Hum. Genet.
, vol.49
, pp. 608-620
-
-
Sherman, S.L.1
Takaesu, N.2
Freeman, S.B.3
Grantham, M.4
Phillips, C.5
Blackston, R.D.6
Jacobs, P.A.7
Cock Well, A.E.8
Freeman, V.9
Uchida, I.10
Mkkelsen, M.11
Kurnit, D.M.12
Buraczynska, M.13
Keats, B.J.B.14
Hassold, T.J.15
-
22
-
-
0017142241
-
Prenatal diagnosis of genetic disease in Canada: Report of collaborative study
-
SIMPSON N.E., DALLAIRE L., MLLER J.R., SIMNOVICH L., HAMERTON J.L., MLLER J., MCKEEN C.: Prenatal diagnosis of genetic disease in Canada: Report of collaborative study. Can. Med. Assoc. J., 1976, 115, 739-746.
-
(1976)
Can. Med. Assoc. J.
, vol.115
, pp. 739-746
-
-
Simpson, N.E.1
Dallaire, L.2
Mller, J.R.3
Simnovich, L.4
Hamerton, J.L.5
Mller, J.6
Mckeen, C.7
-
23
-
-
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(12), 1502-1508.
-
(2000)
J. Med Assoc. Thai.
, vol.83
, Issue.12
, pp. 1502-1508
-
-
Sirivatanapa, P.1
Tongsong, T.2
Wanapirak, C.3
Sirichotiyakul, S.4
Chanprapaph, P.5
Yampochai, A.6
Takapiitra, A.7
Sekararithi, R.8
-
24
-
-
0014021719
-
Chromosome analysis of human amniotic fluid cells
-
STEEL M.W., BREG W.R.: Chromosome analysis of human amniotic fluid cells. Lancet. 1966, i, 383-385.
-
(1966)
Lancet
, vol.1
, pp. 383-385
-
-
Steel, M.W.1
Breg, W.R.2
-
25
-
-
0010433819
-
Tissue culture techniques and chromosome preparation
-
R.S. Verma, A. Babu (eds). New York, McGraw-Hill Press
-
VERMA R.S., BABU A.: Tissue culture techniques and chromosome preparation. In: Human Chromosomes Principles and Techniques. R.S. Verma, A. Babu (eds). New York, McGraw-Hill Press, 1995, 6-71.
-
(1995)
Human Chromosomes Principles and Techniques
, pp. 6-71
-
-
Verma, R.S.1
Babu, A.2
|