-
1
-
-
0029950129
-
Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16, and 22: Their incidence, likely origins, and mechanisms for cell lineage compartmentalization
-
Wolstenholme J: Confined placental mosaicism for trisomies 2, 3, 7, •• 8, 9, 16, and 22: their incidence, likely origins, and mechanisms for cell lineage compartmentalization. Prenat Diagn 1996, 16:511-524.
-
(1996)
Prenat Diagn
, vol.16
, pp. 511-524
-
-
Wolstenholme, J.1
-
2
-
-
0018198093
-
Manufactured hexaparenteral mice show that adults are derived from three embryonic cells
-
Markert C, Petters R: Manufactured hexaparenteral mice show that adults are derived from three embryonic cells. Science 1978, 202:56-58.
-
(1978)
Science
, vol.202
, pp. 56-58
-
-
Markert, C.1
Petters, R.2
-
3
-
-
0008264482
-
Chromosome Analysis Guidelines, Preliminary Report
-
Association of Cytogenetic Technologists: Chromosome Analysis Guidelines, Preliminary Report. Karyo 1989, 6:131-135.
-
(1989)
Karyo
, vol.6
, pp. 131-135
-
-
-
4
-
-
0017347991
-
Exclusion of chromosomal mosaicism: Tables of 90%, 95% and 99% confidence limits and comments on use
-
Hook EB: Exclusion of chromosomal mosaicism: tables of 90%, 95% and 99% confidence limits and comments on use. Am J Hum Genet 1977, 29:94-97.
-
(1977)
Am J Hum Genet
, vol.29
, pp. 94-97
-
-
Hook, E.B.1
-
5
-
-
0027941896
-
Exclusion of chromosomal mosaicism in amniotic fluid cultures: Determination of number colonies needed for accurate analysis
-
Featherstone T, Sheung SW, Spitznagel E, Peakman D: Exclusion of chromosomal mosaicism in amniotic fluid cultures: determination of number colonies needed for accurate analysis. Prenat Diagn 1994, 14:1009-1017.
-
(1994)
Prenat Diagn
, vol.14
, pp. 1009-1017
-
-
Featherstone, T.1
Sheung, S.W.2
Spitznagel, E.3
Peakman, D.4
-
7
-
-
0028866997
-
Is the 15-in situ clone protocol necessary to detect amniotic fluid mosaicism?
-
Cheng EY, Luthy DA, Dunne DFB, Luthardt FW: Is the 15-in situ clone • protocol necessary to detect amniotic fluid mosaicism? Am J Obstet Gynecol 1995, 174:1025-1030.
-
(1995)
Am J Obstet Gynecol
, vol.174
, pp. 1025-1030
-
-
Cheng, E.Y.1
Luthy, D.A.2
Dunne, D.F.B.3
Luthardt, F.W.4
-
8
-
-
0026741249
-
Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies
-
Hsu LYF, Kaffe S, Jenkins EC, Alonso L, Benn PA, David K, Hirschhorn K, Lieber E, Shanske A, Shapiro LR et al.: Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies. Prenat Diagn 1992, 12:555-573.
-
(1992)
Prenat Diagn
, vol.12
, pp. 555-573
-
-
Hsu, L.Y.F.1
Kaffe, S.2
Jenkins, E.C.3
Alonso, L.4
Benn, P.A.5
David, K.6
Hirschhorn, K.7
Lieber, E.8
Shanske, A.9
Shapiro, L.R.10
-
9
-
-
0344623182
-
The role of confined chromosomal mosaicism in placental function and human development
-
Kalousek DH: The role of confined chromosomal mosaicism in placental function and human development. Growth Genet Hormones 1988, 4:1-3.
-
(1988)
Growth Genet Hormones
, vol.4
, pp. 1-3
-
-
Kalousek, D.H.1
-
10
-
-
0021634135
-
United States survey on chromosome mosaicism and pseudomosaicism in prenatal diagnosis
-
Hsu LYF: United States survey on chromosome mosaicism and pseudomosaicism in prenatal diagnosis. Prenat Diagn 1984, 4:97-130.
-
(1984)
Prenat Diagn
, vol.4
, pp. 97-130
-
-
Hsu, L.Y.F.1
-
11
-
-
0003815152
-
Chromosome abnormalities detected at prenatal diagnosis
-
Edited by Gardener RJM, Sutherland GR. New York: Oxford University Press
-
Gardner RJM, Sutherland GR: Chromosome abnormalities detected at prenatal diagnosis. In Chromosome Abnormalities and Genetic Counseling, 2nd edn. Edited by Gardener RJM, Sutherland GR. New York: Oxford University Press; 1996:345-375.
-
(1996)
Chromosome Abnormalities and Genetic Counseling, 2nd Edn.
, pp. 345-375
-
-
Gardner, R.J.M.1
Sutherland, G.R.2
-
12
-
-
0025374943
-
True fetal mosaicism revealed by a single abnormal colony in amniocyte culture
-
Terzoli G, Rossella F, Biscaglia M, Simoni G: True fetal mosaicism revealed by a single abnormal colony in amniocyte culture. Prenat Diagn 1990, 10:273-274.
-
(1990)
Prenat Diagn
, vol.10
, pp. 273-274
-
-
Terzoli, G.1
Rossella, F.2
Biscaglia, M.3
Simoni, G.4
-
13
-
-
8244246270
-
Pseudomosaicism for 4p- In amniotic fluid cell culture proven to be true mosaicism after birth
-
Vockley J, Inserra JA, Breg WR, Yang-Feng TL: Pseudomosaicism for 4p-in amniotic fluid cell culture proven to be true mosaicism after birth. Am J Med Genet 1991, 9:433-437.
-
(1991)
Am J Med Genet
, vol.9
, pp. 433-437
-
-
Vockley, J.1
Inserra, J.A.2
Breg, W.R.3
Yang-Feng, T.L.4
-
14
-
-
0026682553
-
Cytogenetic results from the U.S. collaborative study on CVS
-
Ledbetter DH, Zachary JM, Simpson JL, Golbus MS, Pergament E, Jackson L, Mahoney MJ, Desnick RJ, Schulman J, Copeland KL et al.: Cytogenetic results from the U.S. collaborative study on CVS. Prenat Diagn 1992, 12:317-345.
-
(1992)
Prenat Diagn
, vol.12
, pp. 317-345
-
-
Ledbetter, D.H.1
Zachary, J.M.2
Simpson, J.L.3
Golbus, M.S.4
Pergament, E.5
Jackson, L.6
Mahoney, M.J.7
Desnick, R.J.8
Schulman, J.9
Copeland, K.L.10
-
15
-
-
0024421774
-
The European collaborative study on mosaicism in chorionic villus sampling: Data from 1986 to 1987
-
Vejerslev LO, Kikkelsen M: The European collaborative study on mosaicism in chorionic villus sampling: data from 1986 to 1987. Prenat Diagn 1989, 9:575-588.
-
(1989)
Prenat Diagn
, vol.9
, pp. 575-588
-
-
Vejerslev, L.O.1
Kikkelsen, M.2
-
16
-
-
0025786891
-
Follow-up and pregnancy outcome after a diagnosis of mosaicism in CVS
-
Breed AS, Mantingh A, Vosters R, Beekhuis JR, Van Lith JM, Anders GJ: Follow-up and pregnancy outcome after a diagnosis of mosaicism in CVS. Prenat Diagn 1991, 11:577-580.
-
(1991)
Prenat Diagn
, vol.11
, pp. 577-580
-
-
Breed, A.S.1
Mantingh, A.2
Vosters, R.3
Beekhuis, J.R.4
Van Lith, J.M.5
Anders, G.J.6
-
17
-
-
13344294391
-
Incidence and significance of • chromosomal mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: A collaborative study
-
Hsu LYF, Ming-Tsung Y, Richkind KE: Incidence and significance of • chromosomal mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study. Prenat Diagn 1996, 16:1-28.
-
(1996)
Prenat Diagn
, vol.16
, pp. 1-28
-
-
Hsu, L.Y.F.1
Ming-Tsung, Y.2
Richkind, K.E.3
-
18
-
-
0027159867
-
Follow-up of pregnancies complicated by placental mosaicism diagnosed by chorionic villus sampling
-
Fryburg JS, Dimaio MS, Yang-Feng TL, Mahoney M: Follow-up of pregnancies complicated by placental mosaicism diagnosed by chorionic villus sampling. Prenat Diagn 1993, 13:481-494.
-
(1993)
Prenat Diagn
, vol.13
, pp. 481-494
-
-
Fryburg, J.S.1
Dimaio, M.S.2
Yang-Feng, T.L.3
Mahoney, M.4
-
19
-
-
0025011542
-
Interpretation of chromosome mosaicism and discrepancies in chorionic villi studies
-
Sachs ES, Janoda MGJ, Los FJ, Pupers L, Reuss A, Wladimiroff JW: Interpretation of chromosome mosaicism and discrepancies in chorionic villi studies. Am J Med Genet 1990, 37:268-271.
-
(1990)
Am J Med Genet
, vol.37
, pp. 268-271
-
-
Sachs, E.S.1
Janoda, M.G.J.2
Los, F.J.3
Pupers, L.4
Reuss, A.5
Wladimiroff, J.W.6
-
20
-
-
0027531981
-
Mosaicism in chorionic villus sampling: An analysis of incidence and chromosome involved in 2612 consecutive cases
-
Wang BBT, Rubin CH, Williams J: Mosaicism in chorionic villus sampling: an analysis of incidence and chromosome involved in 2612 consecutive cases. Prenat Diagn 1993, 13:179-190.
-
(1993)
Prenat Diagn
, vol.13
, pp. 179-190
-
-
Wang, B.B.T.1
Rubin, C.H.2
Williams, J.3
-
21
-
-
0028207074
-
The predictive value of cytogenetic diagnosis after CVS based on 4860 cases with both direct and culture methods
-
Pittalis MC, Dalpra L, Torricelli F, Rizzo N, Nocera G, Cariati E, Santarini L, Tibiletti MG, Agosti S, Bovicelli L et al.: The predictive value of cytogenetic diagnosis after CVS based on 4860 cases with both direct and culture methods. Prenat Diagn 1994, 14:267-278.
-
(1994)
Prenat Diagn
, vol.14
, pp. 267-278
-
-
Pittalis, M.C.1
Dalpra, L.2
Torricelli, F.3
Rizzo, N.4
Nocera, G.5
Cariati, E.6
Santarini, L.7
Tibiletti, M.G.8
Agosti, S.9
Bovicelli, L.10
-
22
-
-
0027377012
-
Cytogenetic analysis of 1375 amniotic fluid specimens from pregnancies with gestational age less than 14 weeks
-
Lockwood DH, Neu RL: Cytogenetic analysis of 1375 amniotic fluid specimens from pregnancies with gestational age less than 14 weeks. Prenat Diagn 1993, 13:801-805.
-
(1993)
Prenat Diagn
, vol.13
, pp. 801-805
-
-
Lockwood, D.H.1
Neu, R.L.2
-
23
-
-
0028242891
-
Early amniocentesis - A cytogenetic evaluation of over 1500 cases
-
Eiben B, Goebel R, Hansen S, Hammans W: Early amniocentesis - a cytogenetic evaluation of over 1500 cases. Prenat Diagn 1994, 14:497-501.
-
(1994)
Prenat Diagn
, vol.14
, pp. 497-501
-
-
Eiben, B.1
Goebel, R.2
Hansen, S.3
Hammans, W.4
-
25
-
-
0027449974
-
Fetal blood sampling and cytogenetic abnormalities
-
Liou J, Chen C, Breg WR, Hobbins JC, Mahoney MJ, Yang-Feng TL: Fetal blood sampling and cytogenetic abnormalities. Prenat Diagn 1993, 13:1-8.
-
(1993)
Prenat Diagn
, vol.13
, pp. 1-8
-
-
Liou, J.1
Chen, C.2
Breg, W.R.3
Hobbins, J.C.4
Mahoney, M.J.5
Yang-Feng, T.L.6
-
26
-
-
0002232454
-
Prenatal diagnosis of chromosomal abnormalities through amniocentesis
-
Edited by Milunsky A. Baltimore: The John Hopkins University Press
-
Hsu LYF: Prenatal diagnosis of chromosomal abnormalities through amniocentesis. In Genetic Disorders and the Fetus, 3rd edn. Edited by Milunsky A. Baltimore: The John Hopkins University Press; 1992:155-210.
-
(1992)
Genetic Disorders and the Fetus, 3rd Edn.
, pp. 155-210
-
-
Hsu, L.Y.F.1
-
27
-
-
0011371295
-
Trisomy 16 mosaicism in amniotic fluid cells and poor outcome associated with unexplained elevated maternal-serum alpha-fetoprotein
-
Hajianpour MJ, Randolph LM, Parvizpour D, Habibian R: Trisomy 16 mosaicism in amniotic fluid cells and poor outcome associated with unexplained elevated maternal-serum alpha-fetoprotein [Abstract]. Am J Hum Genet 1992, 51:1613.
-
(1992)
Am J Hum Genet
, vol.51
, pp. 1613
-
-
Hajianpour, M.J.1
Randolph, L.M.2
Parvizpour, D.3
Habibian, R.4
-
28
-
-
0026638252
-
Mosaic trisomy 15 found at amniocentesis
-
Lahdetie JL, Lakkala T: Mosaic trisomy 15 found at amniocentesis. Prenat Diagn 1992, 12:551-552.
-
(1992)
Prenat Diagn
, vol.12
, pp. 551-552
-
-
Lahdetie, J.L.1
Lakkala, T.2
-
29
-
-
0029849830
-
Trisomy 16 mosaicism in amniotic fluid cell cultures
-
Tantravahi U, Matsumoto C, Delanch J, Craffey A, Smeltzer J, Benn P: Trisomy 16 mosaicism in amniotic fluid cell cultures. Prenat Diagn 1996, 16:749-754.
-
(1996)
Prenat Diagn
, vol.16
, pp. 749-754
-
-
Tantravahi, U.1
Matsumoto, C.2
Delanch, J.3
Craffey, A.4
Smeltzer, J.5
Benn, P.6
-
30
-
-
85177155560
-
Prenatal diagnosis of 45,XJ • 46,XX mosaicism and 45,X: Implications for postnatal outcome
-
Koeberi DD, McGillivray B, Sybert VP: Prenatal diagnosis of 45,XJ • 46,XX mosaicism and 45,X: implications for postnatal outcome. Am J Hum Genet 1995, 57:651-660.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 651-660
-
-
Koeberi, D.D.1
McGillivray, B.2
Sybert, V.P.3
-
31
-
-
0029004732
-
A 10-year survey, 1980-1990, of prenatally diagnosed small supernumerary marker chromosomes, identified by FISH analysis. Outcome and follow-up of 14 cases diagnosed in a series of 12699 prenatal samples
-
Brondum-Nielsen K, Mikkelsen M: A 10-year survey, 1980-1990, of prenatally diagnosed small supernumerary marker chromosomes, identified by FISH analysis. Outcome and follow-up of 14 cases diagnosed in a series of 12699 prenatal samples. Prenat Diagn 1995, 15:615-619.
-
(1995)
Prenat Diagn
, vol.15
, pp. 615-619
-
-
Brondum-Nielsen, K.1
Mikkelsen, M.2
-
32
-
-
0023806039
-
Extra embryonic/fetal karyotypic discordance during diagnostic chorionic villus sampling
-
Callan DF, Korban G, Dawson G, Gugasyan L, Krumins EJ, Eichenbaum S, Petrass J, Purvis-Smith S, Smith A, Den Dulk G et al.: Extra embryonic/fetal karyotypic discordance during diagnostic chorionic villus sampling. Prenat Diagn 1988, 8:453-460.
-
(1988)
Prenat Diagn
, vol.8
, pp. 453-460
-
-
Callan, D.F.1
Korban, G.2
Dawson, G.3
Gugasyan, L.4
Krumins, E.J.5
Eichenbaum, S.6
Petrass, J.7
Purvis-Smith, S.8
Smith, A.9
Den Dulk, G.10
-
33
-
-
0028244914
-
Cytogenetic analysis of chorionic villi for prenatal diagnosis: An ACC collaborative study of UK data
-
Association of Clinical Cytogeneticists Working Party on Chorionic Villi in Prenatal Diagnosis: Cytogenetic analysis of chorionic villi for prenatal diagnosis: an ACC collaborative study of UK data. Prenat Diagn 1994, 14:363-379.
-
(1994)
Prenat Diagn
, vol.14
, pp. 363-379
-
-
-
34
-
-
0029801863
-
Maternal serum screening and trisomy 16 confined to the placenta
-
Grolli C, Cerri V, Tarantini M, Bellotti D, Jacobello C, Gianello R, Zanini • R, Lancetti S, Zaglio S: Maternal serum screening and trisomy 16 confined to the placenta. Prenat Diagn 1996, 16:685-689.
-
(1996)
Prenat Diagn
, vol.16
, pp. 685-689
-
-
Grolli, C.1
Cerri, V.2
Tarantini, M.3
Bellotti, D.4
Jacobello, C.5
Gianello, R.6
Zanini, R.7
Lancetti, S.8
Zaglio, S.9
-
35
-
-
0027179033
-
Cytogenetic analysis of 2928 CVS samples and 1075 amniocentesis from randomized studies
-
Smidt-Jensen S, Lind A, Permin M: Cytogenetic analysis of 2928 CVS samples and 1075 amniocentesis from randomized studies. Prenat Diagn 1993, 13:723-740.
-
(1993)
Prenat Diagn
, vol.13
, pp. 723-740
-
-
Smidt-Jensen, S.1
Lind, A.2
Permin, M.3
-
36
-
-
0028242883
-
Trisomy 8 mosaicism in chorionic villus sampling: Case report and counseling issues
-
Klein J, Graham JM, Platt LD, Schreck R: Trisomy 8 mosaicism in chorionic villus sampling: case report and counseling issues. Prenat Diagn 1994, 14:451-454.
-
(1994)
Prenat Diagn
, vol.14
, pp. 451-454
-
-
Klein, J.1
Graham, J.M.2
Platt, L.D.3
Schreck, R.4
-
37
-
-
0029117386
-
Identification of a case of maternal uniparental disomy of chromosome 10 associated with confined placental mosaicism
-
Jones C, Booth C, Rita D, Jazmines L, Spiro R, McCulloch B, McCaskill C, Shaffer LG: Identification of a case of maternal uniparental disomy of chromosome 10 associated with confined placental mosaicism. Prenat Diagn 1995, 15:843-848.
-
(1995)
Prenat Diagn
, vol.15
, pp. 843-848
-
-
Jones, C.1
Booth, C.2
Rita, D.3
Jazmines, L.4
Spiro, R.5
McCulloch, B.6
McCaskill, C.7
Shaffer, L.G.8
-
38
-
-
0029026491
-
Prenatal diagnosis of trisomy 9, six cases and a review of the literature
-
Saura R, Traore W, Taine L, Wen ZQ, Roux D, Maugey-Laulom B, Ruffie M, Vergnaud A, Horovitz J: Prenatal diagnosis of trisomy 9, six cases and a review of the literature. Prenat Diagn 1995, 15:609-614.
-
(1995)
Prenat Diagn
, vol.15
, pp. 609-614
-
-
Saura, R.1
Traore, W.2
Taine, L.3
Wen, Z.Q.4
Roux, D.5
Maugey-Laulom, B.6
Ruffie, M.7
Vergnaud, A.8
Horovitz, J.9
-
39
-
-
0027180953
-
Origin of extraembryonic mesoderm in experienced animals: Relevance to chorionic mosaicism in humans
-
Bianchi DW, Wilkins-Haug LE, Enders AC, Hay ED: Origin of extraembryonic mesoderm in experienced animals: relevance to chorionic mosaicism in humans. Am J Med Genet 1993, 46:542-550.
-
(1993)
Am J Med Genet
, vol.46
, pp. 542-550
-
-
Bianchi, D.W.1
Wilkins-Haug, L.E.2
Enders, A.C.3
Hay, E.D.4
-
40
-
-
0001495044
-
Chromosomal findings in chorionic villi
-
Edited by Vogel F, Sperling K. Heidelberg: Springer-Verlag
-
Middelsen M, Ayme S: Chromosomal findings in chorionic villi. In Human Genetics. Edited by Vogel F, Sperling K. Heidelberg: Springer-Verlag; 1987:597-606.
-
(1987)
Human Genetics
, pp. 597-606
-
-
Middelsen, M.1
Ayme, S.2
-
41
-
-
0021131817
-
European collaborative study on prenatal diagnosis: Mosaicism, pseudomosaicism and single abnormal cells in amniotic fluid cell cultures
-
Bui TH, Iselius L, Linsten J: European collaborative study on prenatal diagnosis: mosaicism, pseudomosaicism and single abnormal cells in amniotic fluid cell cultures. Prenat Diagn 1984, 4:45-62.
-
(1984)
Prenat Diagn
, vol.4
, pp. 45-62
-
-
Bui, T.H.1
Iselius, L.2
Linsten, J.3
-
42
-
-
0029897750
-
Risk of fetal mosaicism when placental mosaicism is diagnosed by chorionic villus sampling
-
Phillips OP, Tharapel AT, Lerner JL, Park VM, Wachtel SS, Shulman LP: Risk of fetal mosaicism when placental mosaicism is diagnosed by chorionic villus sampling. Am J Obstet Gynecol 1996, 174:850-855.
-
(1996)
Am J Obstet Gynecol
, vol.174
, pp. 850-855
-
-
Phillips, O.P.1
Tharapel, A.T.2
Lerner, J.L.3
Park, V.M.4
Wachtel, S.S.5
Shulman, L.P.6
-
43
-
-
0004550166
-
Prenatal diagnosis of trisomy 2 mosaicism confirmed in foreskin fibroblasts
-
Casey J, Ketterer DM, Heisler KL, Daugherty EA, Prince PM, Giles HR: Prenatal diagnosis of trisomy 2 mosaicism confirmed in foreskin fibroblasts [Abstract]. Am J Hum Genet 1990, 47:A270.
-
(1990)
Am J Hum Genet
, vol.47
-
-
Casey, J.1
Ketterer, D.M.2
Heisler, K.L.3
Daugherty, E.A.4
Prince, P.M.5
Giles, H.R.6
-
44
-
-
0024993575
-
Pre- and postnatal diagnosis of trisomy 4 mosaicism
-
Marion J, Femhoff PM, Korotkin J, Priest J: Pre-and postnatal diagnosis of trisomy 4 mosaicism. Am J Med Genet 1990, 37:362-365.
-
(1990)
Am J Med Genet
, vol.37
, pp. 362-365
-
-
Marion, J.1
Femhoff, P.M.2
Korotkin, J.3
Priest, J.4
-
45
-
-
0026764401
-
Trisomy 5 mosaicism detected prenatally with an affected liveborn
-
Sciorra L, Hux C, Day-Salvadore D, Lee M, Mandebaum D, Brady-Yasbin S, Frybury J, Mahoney M, Schoenfeld-Dimaio M: Trisomy 5 mosaicism detected prenatally with an affected liveborn. Prenat Diagn 1992, 12:477-482.
-
(1992)
Prenat Diagn
, vol.12
, pp. 477-482
-
-
Sciorra, L.1
Hux, C.2
Day-Salvadore, D.3
Lee, M.4
Mandebaum, D.5
Brady-Yasbin, S.6
Frybury, J.7
Mahoney, M.8
Schoenfeld-Dimaio, M.9
-
46
-
-
0017192133
-
Trisomy 8 mosaicism: A case report and a proposed list of the clinical features
-
Kosztolanyi E, Buhler EM, Elmiger P, Stadler GR: Trisomy 8 mosaicism: a case report and a proposed list of the clinical features. Eur J Pediatr 1976, 123:293-300.
-
(1976)
Eur J Pediatr
, vol.123
, pp. 293-300
-
-
Kosztolanyi, E.1
Buhler, E.M.2
Elmiger, P.3
Stadler, G.R.4
-
47
-
-
0014493655
-
Disappearance of a 47, XXC + leucocyte cell line in an infant who had previously exhibited 46,XX/ 48,XXC + mosaicism
-
Neu RL, Baigman GJ, Gardner LI: Disappearance of a 47, XXC + leucocyte cell line in an infant who had previously exhibited 46,XX/ 48,XXC + mosaicism. Pediatrics 1969, 43:623-626.
-
(1969)
Pediatrics
, vol.43
, pp. 623-626
-
-
Neu, R.L.1
Baigman, G.J.2
Gardner, L.I.3
-
48
-
-
0016343268
-
Trisomy 8 mosaicism syndrome
-
Schinzel A, Biro Z, Schmid W, Hayashik K: Trisomy 8 mosaicism syndrome. Helv Paediatr Acta 1974, 29:531-540.
-
(1974)
Helv Paediatr Acta
, vol.29
, pp. 531-540
-
-
Schinzel, A.1
Biro, Z.2
Schmid, W.3
Hayashik, K.4
-
49
-
-
0016209025
-
Troubles graves d'intgration du langue de l'enfant et aberrations chromosomiques àpropos de trois cas
-
Debray-Ritzen P, Burszyein C, Vivier R, Rethorek MO, Prieur M, Lejeune J: Troubles graves d'intgration du langue de l'enfant et aberrations chromosomiques àpropos de trois cas. Rev Neurol 1974, 130:357-365.
-
(1974)
Rev Neurol
, vol.130
, pp. 357-365
-
-
Debray-Ritzen, P.1
Burszyein, C.2
Vivier, R.3
Rethorek, M.O.4
Prieur, M.5
Lejeune, J.6
-
50
-
-
0021064865
-
Extremer Gewebe-Mozaizismus bei trisomie 8-syndrome trisomie 8 in fibroblasten bei normalem karyotyp in lymphoxyten
-
Meisel-Stoisiek M, Pfeifer RA, Tietze HU: Extremer Gewebe-Mozaizismus bei trisomie 8-syndrome trisomie 8 in fibroblasten bei normalem karyotyp in lymphoxyten. Klin Pediatr 1993, 195:365-368.
-
(1993)
Klin Pediatr
, vol.195
, pp. 365-368
-
-
Meisel-Stoisiek, M.1
Pfeifer, R.A.2
Tietze, H.U.3
-
51
-
-
0026564634
-
An infant with trisomy 9 mosaicism presenting as a complete trisomy 9 by amniocentesis
-
Sherer D, Wang NN, Thompson H, Peterson J, Miller M, Abramowicz M, Abramowicz J: An infant with trisomy 9 mosaicism presenting as a complete trisomy 9 by amniocentesis. Prenat Diagn 1992, 12:31-37.
-
(1992)
Prenat Diagn
, vol.12
, pp. 31-37
-
-
Sherer, D.1
Wang, N.N.2
Thompson, H.3
Peterson, J.4
Miller, M.5
Abramowicz, M.6
Abramowicz, J.7
-
52
-
-
0027451113
-
Prenatal diagnosis of trisomy 9 mosaicism: Two new cases
-
Merino A, De Perdigo A, Nombalais F, Yvinec M, Le Roux MG, Bellec V: Prenatal diagnosis of trisomy 9 mosaicism: two new cases. Prenat Diagn 1993, 13:1001-1007.
-
(1993)
Prenat Diagn
, vol.13
, pp. 1001-1007
-
-
Merino, A.1
De Perdigo, A.2
Nombalais, F.3
Yvinec, M.4
Le Roux, M.G.5
Bellec, V.6
-
53
-
-
0024436226
-
Prenatal detection of trisomy 9 mosaicism
-
Schwartz S, Ashai S, Meijboom EJ, Schwartx MF, Sun CCJ, Cohen MM: Prenatal detection of trisomy 9 mosaicism. Prenat Diagn 1989, 9:549-554.
-
(1989)
Prenat Diagn
, vol.9
, pp. 549-554
-
-
Schwartz, S.1
Ashai, S.2
Meijboom, E.J.3
Schwartx, M.F.4
Sun, C.C.J.5
Cohen, M.M.6
-
54
-
-
0027492987
-
Prenatal confirmation of trisomy 12 mosaicism by fetal skin biopsy
-
Cartolano R, Guerneri S, Fogliani R, Galimberti A, Nicolini U: Prenatal confirmation of trisomy 12 mosaicism by fetal skin biopsy. Prenat Diagn 1993, 13:1057-1059.
-
(1993)
Prenat Diagn
, vol.13
, pp. 1057-1059
-
-
Cartolano, R.1
Guerneri, S.2
Fogliani, R.3
Galimberti, A.4
Nicolini, U.5
-
55
-
-
0024328319
-
Trisomy 12 mosaicism in amniocytes and dysmorphic child despite normal chromosomes in fetal blood sample
-
Von Koskull H, Ritvanen A, Ämmälä P, Gahmberg N, Salonen R: Trisomy 12 mosaicism in amniocytes and dysmorphic child despite normal chromosomes in fetal blood sample. Prenat Diagn 1989, 9:433-437.
-
(1989)
Prenat Diagn
, vol.9
, pp. 433-437
-
-
Von Koskull, H.1
Ritvanen, A.2
Ämmälä, P.3
Gahmberg, N.4
Salonen, R.5
-
58
-
-
0027981768
-
True trisomy 15 mosaicism, detected by amniocentesis at 12 weeks of gestation and fetal echocardiography
-
Sundberg K, Brocks V, Jacobsen J, Beck B: True trisomy 15 mosaicism, detected by amniocentesis at 12 weeks of gestation and fetal echocardiography. Pren Diagnat 1994, 14:559-563.
-
(1994)
Pren Diagnat
, vol.14
, pp. 559-563
-
-
Sundberg, K.1
Brocks, V.2
Jacobsen, J.3
Beck, B.4
-
59
-
-
0027962406
-
Postnatal confirmation of prenatally diagnosed trisomy 16 mosaicism in two phenotypically abnormal liveborns
-
Pletcher BA, Sanz MM, Schlessel JS, Kunaporn S, McKanna C, Bailer MG, Alonso ML, Zaslav A, Brown WT, Ray JH: Postnatal confirmation of prenatally diagnosed trisomy 16 mosaicism in two phenotypically abnormal liveborns. Prenat Diagn 1994, 14:933-940.
-
(1994)
Prenat Diagn
, vol.14
, pp. 933-940
-
-
Pletcher, B.A.1
Sanz, M.M.2
Schlessel, J.S.3
Kunaporn, S.4
McKanna, C.5
Bailer, M.G.6
Alonso, M.L.7
Zaslav, A.8
Brown, W.T.9
Ray, J.H.10
-
60
-
-
0027420466
-
Mosaic trisomy 16 in a thriving infant; maternal heterodisomy for chromosome 16
-
Lindor MN, Jalal SM, Thibodeau SN, Bonde D, Sauser KL, Karnes PS: Mosaic trisomy 16 in a thriving infant; maternal heterodisomy for chromosome 16. Clin Genet 1993, 44:185-389.
-
(1993)
Clin Genet
, vol.44
, pp. 185-389
-
-
Lindor, M.N.1
Jalal, S.M.2
Thibodeau, S.N.3
Bonde, D.4
Sauser, K.L.5
Karnes, P.S.6
-
61
-
-
0025265179
-
Case report: Mosaic trisomy 16 in a live newborn infant
-
Gilbertson NJ, Taylor JW, Kovar IZ: Case report: mosaic trisomy 16 in a live newborn infant. Arch Dis Child 1990,65:388-389.
-
(1990)
Arch Dis Child
, vol.65
, pp. 388-389
-
-
Gilbertson, N.J.1
Taylor, J.W.2
Kovar, I.Z.3
-
62
-
-
0027180226
-
46,XY/47,XY, + 17p + mosaicism in amniocytes associated with fetal abnormalities despite normal fetal blood karyotype
-
Kingston H, Nicolini U, Haslam J, Andrews T: 46,XY/47,XY, + 17p + mosaicism in amniocytes associated with fetal abnormalities despite normal fetal blood karyotype. Prenat Diag 1993, 13:637-642.
-
(1993)
Prenat Diag
, vol.13
, pp. 637-642
-
-
Kingston, H.1
Nicolini, U.2
Haslam, J.3
Andrews, T.4
-
63
-
-
0030033537
-
A clinical and molecular study of mosaicism for trisomy 17
-
Shaffer LG, McCaskill C, Hersh J, Greenberg F, Lupski JR: A clinical and molecular study of mosaicism for trisomy 17. Hum Genet 1996, 97:69-72.
-
(1996)
Hum Genet
, vol.97
, pp. 69-72
-
-
Shaffer, L.G.1
McCaskill, C.2
Hersh, J.3
Greenberg, F.4
Lupski, J.R.5
-
64
-
-
0018340524
-
Abnormal skin fibroblast cytogenetics in four dysmorphic patients with normal lymphocyte chromosomes
-
Pagon RA, Hall JG, Davenport SLH, Aase J, Norwood TH, Hoehn HW: Abnormal skin fibroblast cytogenetics in four dysmorphic patients with normal lymphocyte chromosomes. Am J Hum Genet 1979, 31:354-361.
-
(1979)
Am J Hum Genet
, vol.31
, pp. 354-361
-
-
Pagon, R.A.1
Hall, J.G.2
Davenport, S.L.H.3
Aase, J.4
Norwood, T.H.5
Hoehn, H.W.6
-
65
-
-
0023429133
-
Trisomy 20 mosaicism in prenatal diagnosis - A review and update
-
Hsu LYF, Kaffe S, Perils TE: Trisomy 20 mosaicism in prenatal diagnosis - a review and update. Prenat Diagn 1987, 7:581-586.
-
(1987)
Prenat Diagn
, vol.7
, pp. 581-586
-
-
Hsu, L.Y.F.1
Kaffe, S.2
Perils, T.E.3
-
66
-
-
0026728680
-
Tissue-specific mosaicism for trisomy 21 and congenital heart disease
-
Yokoyama Y, Narahara K, Kamada M, Tsuji K, Seino Y: Tissue-specific mosaicism for trisomy 21 and congenital heart disease. J Pediatr 1992, 121:80-82.
-
(1992)
J Pediatr
, vol.121
, pp. 80-82
-
-
Yokoyama, Y.1
Narahara, K.2
Kamada, M.3
Tsuji, K.4
Seino, Y.5
-
67
-
-
2642666777
-
Chromosome analysis in a children's hospital. Selection of patients and results of studies
-
Warkany J, Weinstein ED, Soukup SW, Rubinstein JH, Curless MC: Chromosome analysis in a children's hospital. Selection of patients and results of studies. Pediatrics 1964, 33:290-305.
-
(1964)
Pediatrics
, vol.33
, pp. 290-305
-
-
Warkany, J.1
Weinstein, E.D.2
Soukup, S.W.3
Rubinstein, J.H.4
Curless, M.C.5
-
68
-
-
2642620872
-
A mosaic mongol with normal leukocyte chromosomes
-
Ridler MAC, Shaprio A, Delhanty JDA, Smith GF: A mosaic mongol with normal leukocyte chromosomes. Br J Psychiatr 1965, 11:183-185.
-
(1965)
Br J Psychiatr
, vol.11
, pp. 183-185
-
-
Ridler, M.A.C.1
Shaprio, A.2
Delhanty, J.D.A.3
Smith, G.F.4
-
69
-
-
0013980264
-
Mosaic mongolism with normal chromosomal complement in the white blood cells
-
Zellweger H, Abbo G, Nielsen MK, Wallwork K: Mosaic mongolism with normal chromosomal complement in the white blood cells. Humangenetik 1966, 4:323-327.
-
(1966)
Humangenetik
, vol.4
, pp. 323-327
-
-
Zellweger, H.1
Abbo, G.2
Nielsen, M.K.3
Wallwork, K.4
-
70
-
-
0015743368
-
Syndrome de Down avec confirmation de la trisomie G par des cultures de fibroblastes suelement
-
Haberblandt W: Syndrome de Down avec confirmation de la trisomie G par des cultures de fibroblastes suelement J Genet Hum 1973, 21:215-222.
-
(1973)
J Genet Hum
, vol.21
, pp. 215-222
-
-
Haberblandt, W.1
-
71
-
-
0017720611
-
Chromosomal mosaicism in Down's syndrome: A diagnostic challenge
-
Ladda RL, Maisels MJ, Dossett JM, Dobelle Y: Chromosomal mosaicism in Down's syndrome: a diagnostic challenge. Devel Med Child Neurol 1977, 19:668-672.
-
(1977)
Devel Med Child Neurol
, vol.19
, pp. 668-672
-
-
Ladda, R.L.1
Maisels, M.J.2
Dossett, J.M.3
Dobelle, Y.4
-
72
-
-
8244227824
-
Prenatal confirmation of true fetal trisomy 22 mosaicism by fetal skin biopsy following normal fetal blood sampling
-
Berghella V, Wapner RJ, Mahoney MJ, Jackson L, Yang-Feng T: Prenatal confirmation of true fetal trisomy 22 mosaicism by fetal skin biopsy following normal fetal blood sampling [Abstract]. American Society of Human Genetics Meeting, 1996.
-
(1996)
American Society of Human Genetics Meeting
-
-
Berghella, V.1
Wapner, R.J.2
Mahoney, M.J.3
Jackson, L.4
Yang-Feng, T.5
-
73
-
-
0022508825
-
Trisomy 22 mosiacism syndrome and Ullrich Turner stigmata
-
Wertelecki W, Breg WR, Graham JM, Linuma K, Puck SM, Sergovich FR: Trisomy 22 mosiacism syndrome and Ullrich Turner stigmata. Am J Med Genet 1986, 23:739-749.
-
(1986)
Am J Med Genet
, vol.23
, pp. 739-749
-
-
Wertelecki, W.1
Breg, W.R.2
Graham, J.M.3
Linuma, K.4
Puck, S.M.5
Sergovich, F.R.6
-
74
-
-
0023807569
-
Trisomy 22 mosaicism with normal blood chromosomes
-
Lessick MR, Szego K, Wong PWK: Trisomy 22 mosaicism with normal blood chromosomes. Clin Pediatr 1988, 27:451-459.
-
(1988)
Clin Pediatr
, vol.27
, pp. 451-459
-
-
Lessick, M.R.1
Szego, K.2
Wong, P.W.K.3
-
75
-
-
0025295061
-
Trisomy 22 mosaicism limited to skin fibroblasts in a mentally retarded, dysmorphic girl
-
Lund HT, Trane BJ, Aerg L: Trisomy 22 mosaicism limited to skin fibroblasts in a mentally retarded, dysmorphic girl. Acta Paediatr Scand 1990, 79:714-718.
-
(1990)
Acta Paediatr Scand
, vol.79
, pp. 714-718
-
-
Lund, H.T.1
Trane, B.J.2
Aerg, L.3
-
76
-
-
0011966870
-
Trisomy 22 mosaicism and maternal uniparental disomy
-
Desilets VA, Yong SL, Langlois RD, Wilson DK, Kalousek TJ, Pantzar TJ: Trisomy 22 mosaicism and maternal uniparental disomy [Abstract]. Am J Hum Genet 1996, 59:319.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 319
-
-
Desilets, V.A.1
Yong, S.L.2
Langlois, R.D.3
Wilson, D.K.4
Kalousek, T.J.5
Pantzar, T.J.6
-
77
-
-
0025066937
-
Discordant findings in chorionic villus direct preparation and long term culture-mosaicism in the fetus
-
Schlesinger C, Raabe G, Ngo T, Miller K: Discordant findings in chorionic villus direct preparation and long term culture-mosaicism in the fetus. Prenat Diagn 1990, 10:609-612.
-
(1990)
Prenat Diagn
, vol.10
, pp. 609-612
-
-
Schlesinger, C.1
Raabe, G.2
Ngo, T.3
Miller, K.4
-
78
-
-
8244241615
-
Prenatal confirmation of true fetal trisomy 22 mosaicism by fetal skin biopsy following normal fetal blood samplings
-
Berghella V, Wapner RJ, Mahoney M: Prenatal confirmation of true fetal trisomy 22 mosaicism by fetal skin biopsy following normal fetal blood samplings [Abstract]. Am J Hum Genet 1996, 59:1841.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 1841
-
-
Berghella, V.1
Wapner, R.J.2
Mahoney, M.3
-
79
-
-
0019865745
-
Trisomy 7 mosaicism and manifestations of Goldnerhar syndrome with unilateral radial hypoplasia
-
Modes ME, Gleiser S, Paul Derosa G, Yune HY, Girod DA, Weaver DD, Palmer CG: Trisomy 7 mosaicism and manifestations of Goldnerhar syndrome with unilateral radial hypoplasia. J Craniofacial Genet Dev Biol 1981, 1:49-55.
-
(1981)
J Craniofacial Genet Dev Biol
, vol.1
, pp. 49-55
-
-
Modes, M.E.1
Gleiser, S.2
Paul Derosa, G.3
Yune, H.Y.4
Girod, D.A.5
Weaver, D.D.6
Palmer, C.G.7
-
81
-
-
0025753402
-
A revisit of trisomy 20 mosaicism in prenatal diagnosis: An overview of 103 cases
-
Hsu LYF, Kafe S, Perlis TE: A revisit of trisomy 20 mosaicism in prenatal diagnosis: an overview of 103 cases. Prenat Diagn 1991, 11:7-15.
-
(1991)
Prenat Diagn
, vol.11
, pp. 7-15
-
-
Hsu, L.Y.F.1
Kafe, S.2
Perlis, T.E.3
-
82
-
-
0026764401
-
Trisomy 5 mosaicism detected prenatally with an affected livebom
-
Frybury J, Mahoney MJ, Dimaio MS: Trisomy 5 mosaicism detected prenatally with an affected livebom. Prenat Diagn 1992, 12:477-482.
-
(1992)
Prenat Diagn
, vol.12
, pp. 477-482
-
-
Frybury, J.1
Mahoney, M.J.2
Dimaio, M.S.3
-
83
-
-
0026514602
-
Tissue specificity and stability of mosaicism in Pallister-Killian +i(12p) syndrome: Relevance for prenatal diagnosis
-
Priest JH, Rust JM, Fernhoff PM: Tissue specificity and stability of mosaicism in Pallister-Killian +i(12p) syndrome: relevance for prenatal diagnosis. Am J Med Genet 1992, 42:820-824.
-
(1992)
Am J Med Genet
, vol.42
, pp. 820-824
-
-
Priest, J.H.1
Rust, J.M.2
Fernhoff, P.M.3
-
84
-
-
0024835287
-
Down syndrome at birth not detected by first trimester chorionic villus sampling
-
Bartels I, Hansmann I, Holland U, Zoll B, Rauskolb R: Down syndrome at birth not detected by first trimester chorionic villus sampling. Am J Med Genet 1989, 34:606-607.
-
(1989)
Am J Med Genet
, vol.34
, pp. 606-607
-
-
Bartels, I.1
Hansmann, I.2
Holland, U.3
Zoll, B.4
Rauskolb, R.5
-
85
-
-
0025908248
-
Short-term culture and false-negative results for Down's syndrome on chorionic villus sampling
-
Lilford RJ, Caine A, Linton G, Mason G: Short-term culture and false-negative results for Down's syndrome on chorionic villus sampling [Letter] Lancet 1991, 337:861.
-
(1991)
Lancet
, vol.337
, pp. 861
-
-
Lilford, R.J.1
Caine, A.2
Linton, G.3
Mason, G.4
-
86
-
-
0024102348
-
False-negative cytogenetic result in direct preparations after CVS
-
Miny P, Basaran S, Holzgreve W, Horst J, Pawlowitzki IH, Kim NHAN, Ngo T: False-negative cytogenetic result in direct preparations after CVS [Letter]. Prenat Diagn 1988, 8:633.
-
(1988)
Prenat Diagn
, vol.8
, pp. 633
-
-
Miny, P.1
Basaran, S.2
Holzgreve, W.3
Horst, J.4
Pawlowitzki, I.H.5
Kim, N.H.A.N.6
Ngo, T.7
-
87
-
-
0023449299
-
False-positive and false-negative findings on chorionic villus sampling
-
Simoni G, Fraccaro M, Gimelli G, Maggif F, Bricarelli D: False-positive and false-negative findings on chorionic villus sampling. Prenat Diagn 1987, 7:671-672.
-
(1987)
Prenat Diagn
, vol.7
, pp. 671-672
-
-
Simoni, G.1
Fraccaro, M.2
Gimelli, G.3
Maggif, F.4
Bricarelli, D.5
-
88
-
-
0022907964
-
False-negative findings on chorlon villus sampling
-
Martin AO, Elias S, Rosinsky B, Bombard AT, Simpson JL: False-negative findings on chorlon villus sampling. Lancet 1986, ii:391.
-
(1986)
Lancet
, vol.2
, pp. 391
-
-
Martin, A.O.1
Elias, S.2
Rosinsky, B.3
Bombard, A.T.4
Simpson, J.L.5
-
89
-
-
0026629938
-
Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy
-
Cassidy SB, Lai LW, Erickson RP, Magnuson L, Thomas E, Gendron R, Herrmann J: Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy. Am J Hum Genet 1992, 51:701-708.
-
(1992)
Am J Hum Genet
, vol.51
, pp. 701-708
-
-
Cassidy, S.B.1
Lai, L.W.2
Erickson, R.P.3
Magnuson, L.4
Thomas, E.5
Gendron, R.6
Herrmann, J.7
-
90
-
-
0026680691
-
Uniparental disomy 15 resulting from 'correction' of an initial trisomy 15
-
Purvis-Smith SG, Saville T, Manass S, Yip MY, Lam-Po-Tang PR, Duffy B, Johnston H, Leigh D, McDonald B: Uniparental disomy 15 resulting from 'correction' of an initial trisomy 15. Am J Hum Genet 1992, 50:1348-1349.
-
(1992)
Am J Hum Genet
, vol.50
, pp. 1348-1349
-
-
Purvis-Smith, S.G.1
Saville, T.2
Manass, S.3
Yip, M.Y.4
Lam-Po-Tang, P.R.5
Duffy, B.6
Johnston, H.7
Leigh, D.8
McDonald, B.9
-
91
-
-
0029162269
-
Uniparental disomy in humans: Development of an imprinting map and its implications for prenatal diagnosis
-
Ledbetter DH, Engel E: Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis. Hum Mol Genet 1995, 4:1757-1764.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1757-1764
-
-
Ledbetter, D.H.1
Engel, E.2
-
92
-
-
0023197381
-
Confined chorionic mosaicism in prenatal diagnosis
-
Kalousek DK, Dill FJ, Pantzar T, McGillivray BD, Yong SL, Wilson RD: Confined chorionic mosaicism in prenatal diagnosis. Hum Genet 1987, 77:163-167.
-
(1987)
Hum Genet
, vol.77
, pp. 163-167
-
-
Kalousek, D.K.1
Dill, F.J.2
Pantzar, T.3
McGillivray, B.D.4
Yong, S.L.5
Wilson, R.D.6
-
93
-
-
0025272584
-
Mosaicism in chorionic villus sampling: An association with poor perinatal outcome
-
Johnson A, Wapner RJ, Davis GH, Jackson L: Mosaicism in chorionic villus sampling: an association with poor perinatal outcome. Obstet Gynecol 1990, 75:573-577.
-
(1990)
Obstet Gynecol
, vol.75
, pp. 573-577
-
-
Johnson, A.1
Wapner, R.J.2
Davis, G.H.3
Jackson, L.4
-
94
-
-
0026703437
-
Chorionic mosaicism: Association with fetal loss but not with adverse perinatal outcome
-
Wapner RJ, Simpson MS, Golbus MS, Zachary JM, Ledbetter DH, Desnick RJ, Fowler SE, Jackson LG, Lubs H, Mahony RJ et al.: Chorionic mosaicism: association with fetal loss but not with adverse perinatal outcome. Prenat Diagn 1992, 12:347-355.
-
(1992)
Prenat Diagn
, vol.12
, pp. 347-355
-
-
Wapner, R.J.1
Simpson, M.S.2
Golbus, M.S.3
Zachary, J.M.4
Ledbetter, D.H.5
Desnick, R.J.6
Fowler, S.E.7
Jackson, L.G.8
Lubs, H.9
Mahony, R.J.10
-
95
-
-
0025061003
-
Current assessment of fetal losses as a direct consequence of chorionic villus sampling
-
Goldberg JD, Porter AE, Golbus MS: Current assessment of fetal losses as a direct consequence of chorionic villus sampling. Am J Med Genet 1990, 35:174-177.
-
(1990)
Am J Med Genet
, vol.35
, pp. 174-177
-
-
Goldberg, J.D.1
Porter, A.E.2
Golbus, M.S.3
-
96
-
-
0025991931
-
Confirmation of CVS mosaicism in term placentae and high frequency of intrauterine growth retardation association with confined placental mosaicism
-
Kalousek DK, Howard-Pebbles PN, Olson SB, Barrett IJ, Dorfman A, Black SH, Schulman JD, Wilson RD: Confirmation of CVS mosaicism in term placentae and high frequency of intrauterine growth retardation association with confined placental mosaicism. Prenat Diagn 1991, 11:743-750.
-
(1991)
Prenat Diagn
, vol.11
, pp. 743-750
-
-
Kalousek, D.K.1
Howard-Pebbles, P.N.2
Olson, S.B.3
Barrett, I.J.4
Dorfman, A.5
Black, S.H.6
Schulman, J.D.7
Wilson, R.D.8
-
97
-
-
0021135603
-
A Canadian collaborative study of mosaicism in amniotic fluid cell cultures
-
Worton RG, Stem R: A Canadian collaborative study of mosaicism in amniotic fluid cell cultures. Prenat Diagn 1984, 4:131-144.
-
(1984)
Prenat Diagn
, vol.4
, pp. 131-144
-
-
Worton, R.G.1
Stem, R.2
-
98
-
-
0026703437
-
Chorionic mosaicism: Association with fetal loss but not adverse perinatal outcome
-
Wapner RJ, Simpson JL, Golbus MS: Chorionic mosaicism: association with fetal loss but not adverse perinatal outcome. Prenat Diagn 1992, 12:347-355.
-
(1992)
Prenat Diagn
, vol.12
, pp. 347-355
-
-
Wapner, R.J.1
Simpson, J.L.2
Golbus, M.S.3
-
99
-
-
0028290914
-
Confined placental mosaicism, IUGR, and adverse pregnancy outcome: A controlled retrospective UK collaborative study
-
Wolstenholme J, Rooney DE, Davison EV: Confined placental mosaicism, IUGR, and adverse pregnancy outcome: a controlled retrospective UK collaborative study. Prenat Diagn 1994, 14:345-361.
-
(1994)
Prenat Diagn
, vol.14
, pp. 345-361
-
-
Wolstenholme, J.1
Rooney, D.E.2
Davison, E.V.3
-
100
-
-
0029801593
-
The outcome of pregnancies with confined placental chromosome mosaicism in cytotrophoblast cells
-
Leschot NJ, Schuring-Bloom GH, Van Prooijen-Knegt AC, Verjaal M, •• Hansson K, Wolf H, Kanhai HHH, Van Vugt JMG, Christiaens GCML: The outcome of pregnancies with confined placental chromosome mosaicism in cytotrophoblast cells. Prenat Diagn 1996, 16:705-712.
-
(1996)
Prenat Diagn
, vol.16
, pp. 705-712
-
-
Leschot, N.J.1
Schuring-Bloom, G.H.2
Van Prooijen-Knegt, A.C.3
Verjaal, M.4
Hansson, K.5
Wolf, H.6
Kanhai, H.H.H.7
Van Vugt, J.M.G.8
Christiaens, G.C.M.L.9
-
101
-
-
0026482682
-
Rare non-mosaic trisomies in chorionic villus tissue not confirmed at amniocentesis
-
Dorfmann AD, Perszyk J, Robinson P, Black SH, Schulman JD: Rare non-mosaic trisomies in chorionic villus tissue not confirmed at amniocentesis. Prenat Diagn 1992, 12:899-902.
-
(1992)
Prenat Diagn
, vol.12
, pp. 899-902
-
-
Dorfmann, A.D.1
Perszyk, J.2
Robinson, P.3
Black, S.H.4
Schulman, J.D.5
-
102
-
-
0026579503
-
Postnatal placental confirmation of trisomy 2 and trisomy 16 detected at chorionic villus sampling: A possible association with Intrauterine growth retardation and elevated maternal serum alpha-fetoprotein
-
Fryburg JS, Dimaio MS, Mahoney MJ: Postnatal placental confirmation of trisomy 2 and trisomy 16 detected at chorionic villus sampling: a possible association with Intrauterine growth retardation and elevated maternal serum alpha-fetoprotein. Prenat Diagn 1992, 12:481-494.
-
(1992)
Prenat Diagn
, vol.12
, pp. 481-494
-
-
Fryburg, J.S.1
Dimaio, M.S.2
Mahoney, M.J.3
-
103
-
-
0025991931
-
Confirmation of CVS mosaicism in term placentae and high frequency of intrauterine growth retardation association with confined placental mosaicism
-
Kalousek DDK, Howard-Peebles PN, Olson SB, Barrett U, Dorfmann A, Black SH, Schulman JD, Wilson RD: Confirmation of CVS mosaicism in term placentae and high frequency of intrauterine growth retardation association with confined placental mosaicism. Prenat Diagn 1991, 11:743-750.
-
(1991)
Prenat Diagn
, vol.11
, pp. 743-750
-
-
Kalousek, D.D.K.1
Howard-Peebles, P.N.2
Olson, S.B.3
Barrett, U.4
Dorfmann, A.5
Black, S.H.6
Schulman, J.D.7
Wilson, R.D.8
-
104
-
-
0025360413
-
The predictive value of cytogenetic diagnosis after CVS: 1500 cases
-
Breed AS, Mantingh A, Beekhuis JR, Kloosterman MD, Ten Bolscher H, Anders GJ: The predictive value of cytogenetic diagnosis after CVS: 1500 cases. Prenat Diagn 1990, 10:101-110.
-
(1990)
Prenat Diagn
, vol.10
, pp. 101-110
-
-
Breed, A.S.1
Mantingh, A.2
Beekhuis, J.R.3
Kloosterman, M.D.4
Ten Bolscher, H.5
Anders, G.J.6
-
105
-
-
0024343937
-
Chromosome mosaicism of the placenta: A cause of developmental failure of the fetus?
-
Schwinger E, Seidl E, Klink F, Rehder H: Chromosome mosaicism of the placenta: a cause of developmental failure of the fetus? Prenat Diagn 1989, 9:639-647.
-
(1989)
Prenat Diagn
, vol.9
, pp. 639-647
-
-
Schwinger, E.1
Seidl, E.2
Klink, F.3
Rehder, H.4
-
106
-
-
0024458330
-
Seven cases of trisomy 3 mosaicism in chorionic villi
-
Guemeri S, Fortuna R, Romitti L, Bettio D, Simoni G: Seven cases of trisomy 3 mosaicism in chorionic villi. Prenat Diagn 1989, 9:691-698.
-
(1989)
Prenat Diagn
, vol.9
, pp. 691-698
-
-
Guemeri, S.1
Fortuna, R.2
Romitti, L.3
Bettio, D.4
Simoni, G.5
-
107
-
-
0025004331
-
The significance of trisomy 7 mosaicism in chorionic villus cultures
-
Reddy NS, Blakemore KL, Corson SG: The significance of trisomy 7 mosaicism in chorionic villus cultures. Prenat Diagn 1990, 10:417-423.
-
(1990)
Prenat Diagn
, vol.10
, pp. 417-423
-
-
Reddy, N.S.1
Blakemore, K.L.2
Corson, S.G.3
-
108
-
-
0023808742
-
Trisomy 7 in chorionic villi: Follow-up of pregnancy, normal child, and placental clonal anomalies
-
Delozier-Blanchet CD, Engel E, Extermann P, Pastori B: Trisomy 7 in chorionic villi: follow-up of pregnancy, normal child, and placental clonal anomalies. Prenat Diagn 1988, 8:281-286.
-
(1988)
Prenat Diagn
, vol.8
, pp. 281-286
-
-
Delozier-Blanchet, C.D.1
Engel, E.2
Extermann, P.3
Pastori, B.4
-
110
-
-
0026661092
-
Trisomy 16 confined to chorionic villi and unfavourable outcome of pregnancy
-
Simoni G, Brambati B, Maggi F, Jackson L: Trisomy 16 confined to chorionic villi and unfavourable outcome of pregnancy. Ann Genet 1992, 35:110-112.
-
(1992)
Ann Genet
, vol.35
, pp. 110-112
-
-
Simoni, G.1
Brambati, B.2
Maggi, F.3
Jackson, L.4
-
111
-
-
0024996869
-
Intrauterine growth retardation associated with chromosomal aneuploidy confined to the placenta. Three observations: Triple trisomy 6, 21, 22; trisomy 16; and trisomy 18
-
Kennerknecht I, Tende R: Intrauterine growth retardation associated with chromosomal aneuploidy confined to the placenta. Three observations: triple trisomy 6, 21, 22; trisomy 16; and trisomy 18. Prenat Diagn 1990, 10:539-544.
-
(1990)
Prenat Diagn
, vol.10
, pp. 539-544
-
-
Kennerknecht, I.1
Tende, R.2
-
112
-
-
0024361809
-
Trisomy 16 detected at chorion villus sampling
-
Hashish AF, Monk NA, Lovell-Smith MP, Bardwell LM, Fiddes TM, Gardner RJ: Trisomy 16 detected at chorion villus sampling. Prenat Diagn 1989, 9:427-432.
-
(1989)
Prenat Diagn
, vol.9
, pp. 427-432
-
-
Hashish, A.F.1
Monk, N.A.2
Lovell-Smith, M.P.3
Bardwell, L.M.4
Fiddes, T.M.5
Gardner, R.J.6
-
113
-
-
0024325406
-
Non-mosaic trisomy 16 confined to villi
-
Verp MS, Rosinksy B, Sheikh Z, Amarose AP: Non-mosaic trisomy 16 confined to villi. Lancet 1989, ii:915-916.
-
(1989)
Lancet
, vol.2
, pp. 915-916
-
-
Verp, M.S.1
Rosinksy, B.2
Sheikh, Z.3
Amarose, A.P.4
-
114
-
-
0024342350
-
Resorbed co-twin as an explanation for discrepant chorionic villus results: Non-mosaic 47,XX + 16 in villi (direct and culture) with normal (46,XX) amniotic fluid and neonatal blood
-
Tharapel AT, Elias S, Shulman LP, Seely L, Emerson DS, Simpson JL: Resorbed co-twin as an explanation for discrepant chorionic villus results: non-mosaic 47,XX + 16 in villi (direct and culture) with normal (46,XX) amniotic fluid and neonatal blood. Prenat Diagn 1989, 9:467-472.
-
(1989)
Prenat Diagn
, vol.9
, pp. 467-472
-
-
Tharapel, A.T.1
Elias, S.2
Shulman, L.P.3
Seely, L.4
Emerson, D.S.5
Simpson, J.L.6
-
115
-
-
84994968990
-
Apparent non-mosaic trisomy 16 in chorionic villi: Diagnostic dilemma or clinically significant finding
-
Wiliiams J, Wang B, Rubin C, Clark R, Mohandas T: Apparent non-mosaic trisomy 16 in chorionic villi: diagnostic dilemma or clinically significant finding [Abstract]. Am J Hum Genet 1989, 45:273 .
-
(1989)
Am J Hum Genet
, vol.45
, pp. 273
-
-
Wiliiams, J.1
Wang, B.2
Rubin, C.3
Clark, R.4
Mohandas, T.5
-
116
-
-
0027474269
-
Uniparental disomy for chromosome 16 in humans
-
Kalousek DK, Langolois S, Barretti I, Yam I, Wilson DR, Howard-Pebbles PN, Johnson MP, Giorgiutti E: Uniparental disomy for chromosome 16 in humans. Am J Hum Genet 1993, 52:8-16.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 8-16
-
-
Kalousek, D.K.1
Langolois, S.2
Barretti, I.3
Yam, I.4
Wilson, D.R.5
Howard-Pebbles, P.N.6
Johnson, M.P.7
Giorgiutti, E.8
-
117
-
-
0025742914
-
Trisomy 18 in chorionic villus sampling: Problems and consequences
-
Wirtz A, Gloning K-PH, Murken J: Trisomy 18 in chorionic villus sampling: problems and consequences. Prenat Diagn 1991, 11:563-567.
-
(1991)
Prenat Diagn
, vol.11
, pp. 563-567
-
-
Wirtz, A.1
Gloning, K.-P.H.2
Murken, J.3
-
118
-
-
0024359207
-
Trisomic 22 placenta in a case of severe intrauterine growth retardation
-
Stioui S, Desilvestris M, Molinari A, Stripparo L, Shisoni L, Simoni G: Trisomic 22 placenta In a case of severe intrauterine growth retardation. Prenat Diagn 1989, 9:673-676.
-
(1989)
Prenat Diagn
, vol.9
, pp. 673-676
-
-
Stioui, S.1
Desilvestris, M.2
Molinari, A.3
Stripparo, L.4
Shisoni, L.5
Simoni, G.6
-
119
-
-
0028938050
-
Chorionic villus sampling
-
Brambati B, Chorionic villus sampling. Curr Opin Obstet Gynecol 1995, 7:109-116.
-
(1995)
Curr Opin Obstet Gynecol
, vol.7
, pp. 109-116
-
-
Brambati, B.1
|