-
1
-
-
0026445152
-
Association between confined placental trisomy, fetal uniparental disomy, and early intrauterine growth retardation
-
Bennett, P., Vaughan, J., Henderson, D., Loughna, S., Moore, G. (1992). Association between confined placental trisomy, fetal uniparental disomy, and early intrauterine growth retardation, Lancet, 340, 1284-1285.
-
(1992)
Lancet
, vol.340
, pp. 1284-1285
-
-
Bennett, P.1
Vaughan, J.2
Henderson, D.3
Loughna, S.4
Moore, G.5
-
2
-
-
0029998013
-
Clinical significance of placenta-confined nonmosaic trisomy 16
-
Brandenburg, H., Los, F.J., In 't Veld, P. (1996). Clinical significance of placenta-confined nonmosaic trisomy 16, Am. J. Obstet. Gynecol., 174, 1663-1664.
-
(1996)
Am. J. Obstet. Gynecol.
, vol.174
, pp. 1663-1664
-
-
Brandenburg, H.1
Los, F.J.2
In 't Veld, P.3
-
3
-
-
0023840501
-
An embryogenic model to explain cytogenetic inconsistencies observed in chorionic villus versus fetal tissue
-
Crane, J.P., Cheung, S.W. (1988). An embryogenic model to explain cytogenetic inconsistencies observed in chorionic villus versus fetal tissue, Prenat. Diagn., 8, 119-129.
-
(1988)
Prenat. Diagn.
, vol.8
, pp. 119-129
-
-
Crane, J.P.1
Cheung, S.W.2
-
4
-
-
0027317476
-
Variable clinical expression of mosaic trisomy 16 in the newborn infant
-
Devi, A.S., Velinov, M., Kamath, M.V., Eisenfeld, L., Neu, R., Ciarleglio, L., Greenstein, R., Benn, P. (1993). Variable clinical expression of mosaic trisomy 16 in the newborn infant, Am. J. Med. Genet., 47, 294-298.
-
(1993)
Am. J. Med. Genet.
, vol.47
, pp. 294-298
-
-
Devi, A.S.1
Velinov, M.2
Kamath, M.V.3
Eisenfeld, L.4
Neu, R.5
Ciarleglio, L.6
Greenstein, R.7
Benn, P.8
-
5
-
-
0022587147
-
Two subsets of human alphoid repetitive DNA show distinct preferential localization in the pericentric regions of chromosomes 13, 18, and 21
-
Devilee, P., Cremer, T., Slagboom, P., Bakker, E., Scholl, H.P., Hager, H.D., Stevenson, A.F.G., Cornelisse, C.J., Pearson, P.L. (1986). Two subsets of human alphoid repetitive DNA show distinct preferential localization in the pericentric regions of chromosomes 13, 18, and 21, Cytogenet. Cell Genet., 41, 193-201.
-
(1986)
Cytogenet. Cell Genet.
, vol.41
, pp. 193-201
-
-
Devilee, P.1
Cremer, T.2
Slagboom, P.3
Bakker, E.4
Scholl, H.P.5
Hager, H.D.6
Stevenson, A.F.G.7
Cornelisse, C.J.8
Pearson, P.L.9
-
6
-
-
0026450716
-
Uniparental disomy with normal phenotype
-
Dworniczak, B., Koppers, B., Kuriemann, G., Holzgreve, W., Horst, J., Miny, P. (1992). Uniparental disomy with normal phenotype, Lancet, 340, 1285.
-
(1992)
Lancet
, vol.340
, pp. 1285
-
-
Dworniczak, B.1
Koppers, B.2
Kuriemann, G.3
Holzgreve, W.4
Horst, J.5
Miny, P.6
-
7
-
-
0018939994
-
A new genetic concept: Uniparental disomy and its potential effect, isodisomy
-
Engel, E. (1980). A new genetic concept: uniparental disomy and its potential effect, isodisomy, Am. J. Med. Genet., 6, 137-143.
-
(1980)
Am. J. Med. Genet.
, vol.6
, pp. 137-143
-
-
Engel, E.1
-
8
-
-
0025773075
-
Uniparental disomy, isodisomy, and imprinting: Probable effects in man and strategies for their detection
-
Engel, E., DeLoizier-Blanchet, C.D. (1991). Uniparental disomy, isodisomy, and imprinting: probable effects in man and strategies for their detection, Am. J. Hum. Genet., 40, 432-439.
-
(1991)
Am. J. Hum. Genet.
, vol.40
, pp. 432-439
-
-
Engel, E.1
DeLoizier-Blanchet, C.D.2
-
9
-
-
0023222729
-
A simple technique for obtaining high quality chromosome preparations from chorionic villus samples using FdU synchronization
-
Gibas, L.M., Grujic, S., Barr, M.A., Jackson, L.G. (1987). A simple technique for obtaining high quality chromosome preparations from chorionic villus samples using FdU synchronization, Prenat. Diagn., 7, 323-327.
-
(1987)
Prenat. Diagn.
, vol.7
, pp. 323-327
-
-
Gibas, L.M.1
Grujic, S.2
Barr, M.A.3
Jackson, L.G.4
-
10
-
-
0025061003
-
Current assessment of fetal losses as a direct consequence of chorionic villus sampling
-
Goldberg, J.D., Porter, A.E., Golbus, M.S. (1990). Current assessment of fetal losses as a direct consequence of chorionic villus sampling, Am. J. Med. Genet., 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
-
11
-
-
0029118422
-
Recombination and maternal age-dependent non-disjunction: Molecular studies of trisomy 16
-
Hassold, T., Merrill, M., Adkins, K., Freeman, S., Sherman, S. (1995). Recombination and maternal age-dependent non-disjunction: molecular studies of trisomy 16, Am. J. Hum. Genet., 57, 867-874.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 867-874
-
-
Hassold, T.1
Merrill, M.2
Adkins, K.3
Freeman, S.4
Sherman, S.5
-
12
-
-
0025092497
-
Transabdominal villus sampling in early second trimester: A safe sampling method for women of advanced age
-
Jahoda, M.G.J., Pijpers, L., Reuss, A., Brandenburg, H., Cohen-Overbeek, T.E., Los, F.J., Sachs, E.S., Wladimiroff, J.W. (1990). Transabdominal villus sampling in early second trimester: a safe sampling method for women of advanced age, Prenat. Diagn., 10, 307-311.
-
(1990)
Prenat. Diagn.
, vol.10
, pp. 307-311
-
-
Jahoda, M.G.J.1
Pijpers, L.2
Reuss, A.3
Brandenburg, H.4
Cohen-Overbeek, T.E.5
Los, F.J.6
Sachs, E.S.7
Wladimiroff, J.W.8
-
13
-
-
0025272584
-
Mosaicism in chorionic villus sampling: An association with poor perinatal outcome
-
Johnson, A., Wapner, R.J., Davis, G.H., Jackson, L.G. (1990). Mosaicism in chorionic villus sampling: an association with poor perinatal outcome, Obstet. Gynecol., 75, 573-577.
-
(1990)
Obstet. Gynecol.
, vol.75
, pp. 573-577
-
-
Johnson, A.1
Wapner, R.J.2
Davis, G.H.3
Jackson, L.G.4
-
14
-
-
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, L.G. (1995). Identification of a case of maternal uniparental disomy of chromosome 10 associated with confined placental mosaicism, Prenat. Diagn., 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
-
15
-
-
0028676108
-
Genomic imprinting related to prenatal diagnosis
-
Kalousek, D.K., Barrett, I. (1994). Genomic imprinting related to prenatal diagnosis, Prenat. Diagn., 14, 1191-1201.
-
(1994)
Prenat. Diagn.
, vol.14
, pp. 1191-1201
-
-
Kalousek, D.K.1
Barrett, I.2
-
16
-
-
0030055570
-
Confined placental mosaicism
-
Kalousek, D.K., Vekemans, M. (1996). Confined placental mosaicism, J. Med. Genet., 33 (7), 529-533.
-
(1996)
J. Med. Genet.
, vol.33
, Issue.7
, pp. 529-533
-
-
Kalousek, D.K.1
Vekemans, M.2
-
17
-
-
0025991931
-
Confirmation of CVS mosaicism in term placentae and high frequency of intrauterine growth retardation association with confined placental mosaicism
-
Kalousek, D.K., Howard-Peebles, P.N., Olson, S.B., Barrett, I.J., Dorfman, A., Black, S.H., Schulman, J.D., Wilson, R.D. (1991). Confirmation of CVS mosaicism in term placentae and high frequency of intrauterine growth retardation association with confined placental mosaicism, Prenat. Diagn., 11, 743-750.
-
(1991)
Prenat. Diagn.
, vol.11
, pp. 743-750
-
-
Kalousek, D.K.1
Howard-Peebles, 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
-
18
-
-
0027474269
-
Uniparental disomy for chromosome 16 in humans
-
Kalousek, D.K., Langlois, S., Barrett, I., Yam, I., Wilson, D.R., Howard-Peebles, P.N., Johnson, M.P., Giorgiutti, E. (1993). Uniparental disomy for chromosome 16 in humans, Am. J. Hum. Genet., 52, 8-16.
-
(1993)
Am. J. Hum. Genet.
, vol.52
, pp. 8-16
-
-
Kalousek, D.K.1
Langlois, S.2
Barrett, I.3
Yam, I.4
Wilson, D.R.5
Howard-Peebles, P.N.6
Johnson, M.P.7
Giorgiutti, E.8
-
19
-
-
0029852041
-
Trisomy 7 CVS mosaicism: Pregnancy outcome, placental and DNA analysis in 14 cases
-
Kalousek, D.K., Langlois, S., Robinson, W.P., Telenius, A., Bernard, L., Barrett, I.J., Howard-Peebles, P.N., Wilson, R.D. (1996). Trisomy 7 CVS mosaicism: pregnancy outcome, placental and DNA analysis in 14 cases, Am. J. Med. Genet., 65, 348-352.
-
(1996)
Am. J. Med. Genet.
, vol.65
, pp. 348-352
-
-
Kalousek, D.K.1
Langlois, S.2
Robinson, W.P.3
Telenius, A.4
Bernard, L.5
Barrett, I.J.6
Howard-Peebles, P.N.7
Wilson, R.D.8
-
21
-
-
0028097992
-
The utilization of interphase cytogenetic analysis for the detection of mosaicism
-
Lomax, B.L., Kalousek, D.K., Kuchinka, B.D., Barrett, I.J., Harrison, K.J., Safavi, H. (1994). The utilization of interphase cytogenetic analysis for the detection of mosaicism, Hum. Genet., 93, 243-247.
-
(1994)
Hum. Genet.
, vol.93
, pp. 243-247
-
-
Lomax, B.L.1
Kalousek, D.K.2
Kuchinka, B.D.3
Barrett, I.J.4
Harrison, K.J.5
Safavi, H.6
-
22
-
-
0025115707
-
Localization and polymorphism of a chromosome 12-specific a satellite DNA sequence
-
Looijenga, L.H.J., Smit, V.T.H.B.M., Wessels, J.W., Mollevanger, P., Oosterhuis, J.W., Cornelisse, C.J., Devilee, P. (1990). Localization and polymorphism of a chromosome 12-specific a satellite DNA sequence, Cytogenet. Cell Genet., 53, 216-218.
-
(1990)
Cytogenet. Cell Genet.
, vol.53
, pp. 216-218
-
-
Looijenga, L.H.J.1
Smit, V.T.H.B.M.2
Wessels, J.W.3
Mollevanger, P.4
Oosterhuis, J.W.5
Cornelisse, C.J.6
Devilee, P.7
-
23
-
-
26544452282
-
Uniparental disomies after prenatal diagnosis of confined placental mosaicism and intrauterine growth retardation
-
Jerusalem, Israel
-
Miny, P., Koppers, B., Bogdanova, N., Exeler, R., Holzgreve, W., Horst, J., Dworniczak, B. (1994). Uniparental disomies after prenatal diagnosis of confined placental mosaicism and intrauterine growth retardation, 7th International Conference on Early Prenatal Diagnosis, Jerusalem, Israel, A22.
-
(1994)
7th International Conference on Early Prenatal Diagnosis
-
-
Miny, P.1
Koppers, B.2
Bogdanova, N.3
Exeler, R.4
Holzgreve, W.5
Horst, J.6
Dworniczak, B.7
-
24
-
-
0023616290
-
Human chromosome-specific repetitive DNA sequences: Novel markers for genetic analysis
-
Moyzis, R.K., Albright, K.L., Bartholdi, M.F., Cram, L.S., Deaven, L.L., Hildebrand, C.E., Joste, N.E., Longmire, J.L., Meyne, J., Schwarzacher-Robinson, T. (1987). Human chromosome-specific repetitive DNA sequences: novel markers for genetic analysis, Chromosoma (Berlin), 95, 375-386.
-
(1987)
Chromosoma (Berlin)
, vol.95
, pp. 375-386
-
-
Moyzis, R.K.1
Albright, K.L.2
Bartholdi, M.F.3
Cram, L.S.4
Deaven, L.L.5
Hildebrand, C.E.6
Joste, N.E.7
Longmire, J.L.8
Meyne, J.9
Schwarzacher-Robinson, T.10
-
25
-
-
0029075628
-
Positional mapping of loci in the DiGeorge critical region at chromosome 22q11 using a new marker (D22S183)
-
Mulder, M.P., Wilke, M., Langeveld, A., Wilming, L.G., Hagemeijer, A., van Drunen, E., Zwarthoff, E.C., Riegman, P.H.J., Deelen, W.H., van den Ouweland, A.M.W., Halley, D.J.J., Meijers, C. (1995). Positional mapping of loci in the DiGeorge critical region at chromosome 22q11 using a new marker (D22S183), Hum. Genet., 96, 133-141.
-
(1995)
Hum. Genet.
, vol.96
, pp. 133-141
-
-
Mulder, M.P.1
Wilke, M.2
Langeveld, A.3
Wilming, L.G.4
Hagemeijer, A.5
Van Drunen, E.6
Zwarthoff, E.C.7
Riegman, P.H.J.8
Deelen, W.H.9
Van Den Ouweland, A.M.W.10
Halley, D.J.J.11
Meijers, C.12
-
26
-
-
0029820521
-
Case report: Uniparental disomy 16 in association with congenital heart disease
-
O'Riordan, S., Greenough, A., Moore, G.E., Bennett, P., Nicolaides, K.H. (1996). Case report: uniparental disomy 16 in association with congenital heart disease, Prenat. Diagn., 16, 963-965.
-
(1996)
Prenat. Diagn.
, vol.16
, pp. 963-965
-
-
O'Riordan, S.1
Greenough, A.2
Moore, G.E.3
Bennett, P.4
Nicolaides, K.H.5
-
27
-
-
0026680691
-
Uniparental disomy 15 resulting from 'correction' of an initial trisomy 15
-
Purvis-Smith, S.G., Saville, T., Manass, S., Yip, M.-Y., Lam-Po-Tang, P.R.L., Duffy, B., Johnston, H., Leigh, D., McDonald, B. (1992). Uniparental disomy 15 resulting from 'correction' of an initial trisomy 15, Am. J. Hum. Genet., 50, 1348-1350.
-
(1992)
Am. J. Hum. Genet.
, vol.50
, pp. 1348-1350
-
-
Purvis-Smith, S.G.1
Saville, T.2
Manass, S.3
Yip, M.-Y.4
Lam-Po-Tang, P.R.L.5
Duffy, B.6
Johnston, H.7
Leigh, D.8
McDonald, B.9
-
28
-
-
16944367292
-
Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction
-
Robinson, W.P., Barrett, I.J., Bernard, L., Telenius, A., Bernasconi, F., Wilson, R.D., Best, R.G., Howard-Peebles, P.N., Langlois, S., Kalousek, D.K. (1997). Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction, Am. J. Hum. Genet., 60, 917-927.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 917-927
-
-
Robinson, W.P.1
Barrett, I.J.2
Bernard, L.3
Telenius, A.4
Bernasconi, F.5
Wilson, R.D.6
Best, R.G.7
Howard-Peebles, P.N.8
Langlois, S.9
Kalousek, D.K.10
-
29
-
-
0030472329
-
Comprehensive 4-year follow-up on a case of maternal heterodisomy for chromosome 16
-
Schneider, A.S., Bischoff, F.Z., McCaskill, C., Luz Coady, M., Stopfer, J.E., Shaffer, L.G. (1996). Comprehensive 4-year follow-up on a case of maternal heterodisomy for chromosome 16, Am. J. Med. Genet., 66, 204-208.
-
(1996)
Am. J. Med. Genet.
, vol.66
, pp. 204-208
-
-
Schneider, A.S.1
Bischoff, F.Z.2
McCaskill, C.3
Luz Coady, M.4
Stopfer, J.E.5
Shaffer, L.G.6
-
30
-
-
0029848905
-
Analysis of nine pregnancies with confined placental mosaicism for trisomy 2
-
Shaffer, L.G., Langlois, S., McCaskill, C., Main, D.M., Robinson, W.P., Barrett, I.J., Kalousek, D.K. (1996). Analysis of nine pregnancies with confined placental mosaicism for trisomy 2, Prenat. Diagn., 16, 899-905.
-
(1996)
Prenat. Diagn.
, vol.16
, pp. 899-905
-
-
Shaffer, L.G.1
Langlois, S.2
McCaskill, C.3
Main, D.M.4
Robinson, W.P.5
Barrett, I.J.6
Kalousek, D.K.7
-
31
-
-
0023897290
-
Uniparental disomy as a mechanism for human genetic disease
-
Spence, J.E., Perciaccante, R.G., Greig, G.M., Willad, H.F., Ledbetter, D.H., Hejtmancik, J.F., Pollack, M.S., O'Brien, W.E., Beaudet, A.L. (1988). Uniparental disomy as a mechanism for human genetic disease, Am. J. Hum. Genet., 42, 217-226.
-
(1988)
Am. J. Hum. Genet.
, vol.42
, pp. 217-226
-
-
Spence, J.E.1
Perciaccante, R.G.2
Greig, G.M.3
Willad, H.F.4
Ledbetter, D.H.5
Hejtmancik, J.F.6
Pollack, M.S.7
O'Brien, W.E.8
Beaudet, A.L.9
-
32
-
-
0011340139
-
Maternal isodisomy 16 in a normal 46,XX following trisomic conception
-
Sutcliffe, M.J., Mueller, O.T., Gallardo, L.A., Papenhausen, P.R., Tedesco, T.A. (1993). Maternal isodisomy 16 in a normal 46,XX following trisomic conception, Am. J. Hum. Genet., 53 (Suppl.), A1464.
-
(1993)
Am. J. Hum. Genet.
, vol.53
, Issue.SUPPL.
-
-
Sutcliffe, M.J.1
Mueller, O.T.2
Gallardo, L.A.3
Papenhausen, P.R.4
Tedesco, T.A.5
-
33
-
-
0029849830
-
Trisomy 16 mosaicism in amniotic fluid cell cultures
-
Tantravahi, U., Matsumoto, C., Delach, J., Craffey, A., Smeltzer, J., Benn, P. (1996). Trisomy 16 mosaicism in amniotic fluid cell cultures, Prenat. Diagn., 16, 749-754.
-
(1996)
Prenat. Diagn.
, vol.16
, pp. 749-754
-
-
Tantravahi, U.1
Matsumoto, C.2
Delach, J.3
Craffey, A.4
Smeltzer, J.5
Benn, P.6
-
34
-
-
0027172192
-
Fetal aneuploidy diagnosed by fluorescence in situ hybridization within 24 hours after amniocentesis
-
Van Opstal, D., Van Hemel, J.O., Sachs, E.S. (1993). Fetal aneuploidy diagnosed by fluorescence in situ hybridization within 24 hours after amniocentesis, Lancet, 342, 802.
-
(1993)
Lancet
, vol.342
, pp. 802
-
-
Van Opstal, D.1
Van Hemel, J.O.2
Sachs, E.S.3
-
35
-
-
0028798660
-
Retrospective study of trisomy 18 in chorionic villi with fluorescent in situ hybridization on archival direct preparations
-
Van Opstal, D., van den Berg, C., Jahoda, M.G.J., Brandenburg, H., Los, F.J., in 't Veld, P.A. (1995). Retrospective study of trisomy 18 in chorionic villi with fluorescent in situ hybridization on archival direct preparations, Prenat. Diagn., 15, 51-55.
-
(1995)
Prenat. Diagn.
, vol.15
, pp. 51-55
-
-
Van Opstal, D.1
Van Den Berg, C.2
Jahoda, M.G.J.3
Brandenburg, H.4
Los, F.J.5
In 't Veld, P.A.6
-
36
-
-
0027941823
-
Human maternal uniparental disomy for chromosome 16 and fetal development
-
Vaughan, J., Ali, Z., Bower, S., Bennett, P., Chard, T., Moore, G. (1994). Human maternal uniparental disomy for chromosome 16 and fetal development, Prenat. Diagn., 14, 751-756.
-
(1994)
Prenat. Diagn.
, vol.14
, pp. 751-756
-
-
Vaughan, J.1
Ali, Z.2
Bower, S.3
Bennett, P.4
Chard, T.5
Moore, G.6
-
37
-
-
0024372937
-
Chromosome specificity of satellite DNAs: Short- and long-range organization of a diverged dimeric subset of human alpha satellite from chromosome 3
-
Waye, J.S., Willard, H.F. (1989). Chromosome specificity of satellite DNAs: short-and long-range organization of a diverged dimeric subset of human alpha satellite from chromosome 3, Chromosoma, 97, 475-480.
-
(1989)
Chromosoma
, vol.97
, pp. 475-480
-
-
Waye, J.S.1
Willard, H.F.2
-
38
-
-
0023064191
-
Genomic organization of alpha satellite DNA on human chromosome 7: Evidence for two distinct alphoid domains on a single chromosome
-
Waye, J.S., England, S.B., Willard, H.F. (1987). Genomic organization of alpha satellite DNA on human chromosome 7: evidence for two distinct alphoid domains on a single chromosome, Mol. Cell. Biol., 7, 349-356.
-
(1987)
Mol. Cell. Biol.
, vol.7
, pp. 349-356
-
-
Waye, J.S.1
England, S.B.2
Willard, H.F.3
-
39
-
-
0029079282
-
Uniparental isodisomy for chromosome 16 in a growth-retarded infant with congenital heart disease
-
Whiteford, M.L., Coutts, J., Al-Roomi, L., Mather, A., Lowther, G., Cooke, A., Vaughan, J.I., Moore, G.E., Tolmie, J.L. (1995). Uniparental isodisomy for chromosome 16 in a growth-retarded infant with congenital heart disease, Prenat. Diagn., 15, 579-584.
-
(1995)
Prenat. Diagn.
, vol.15
, pp. 579-584
-
-
Whiteford, M.L.1
Coutts, J.2
Al-Roomi, L.3
Mather, A.4
Lowther, G.5
Cooke, A.6
Vaughan, J.I.7
Moore, G.E.8
Tolmie, J.L.9
-
40
-
-
0029886674
-
A case of maternal uniparental disomy of chromosome 9 in association with confined placental mosaicism for trisomy 9
-
Wilkinson, T.A., James, R.S., Crolla, J.A., Cockwell, A.E., Campbell, P.L., Temple, I.K. (1996). A case of maternal uniparental disomy of chromosome 9 in association with confined placental mosaicism for trisomy 9, Prenat. Diagn., 16, 371-374.
-
(1996)
Prenat. Diagn.
, vol.16
, pp. 371-374
-
-
Wilkinson, T.A.1
James, R.S.2
Crolla, J.A.3
Cockwell, A.E.4
Campbell, P.L.5
Temple, I.K.6
-
41
-
-
0021100775
-
Isolation and characterization of a major tandem repeat family from the human X chromosome
-
Willard, H.F., Smith, K.D., Sutherland, J. (1983). Isolation and characterization of a major tandem repeat family from the human X chromosome, Nucleic Acids Res., 11, 2017-2033.
-
(1983)
Nucleic Acids Res.
, vol.11
, pp. 2017-2033
-
-
Willard, H.F.1
Smith, K.D.2
Sutherland, J.3
-
42
-
-
0028925188
-
An audit of trisomy 16 in man
-
Wolstenholme, J. (1995). An audit of trisomy 16 in man, Prenat. Diagn., 15, 109-121.
-
(1995)
Prenat. Diagn.
, vol.15
, pp. 109-121
-
-
Wolstenholme, J.1
-
43
-
-
0029950129
-
Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, and 22: Their incidence, likely origins, and mechanisms for cell lineage compartmentalization
-
Wolstenholme, J. (1996). Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, and 22: their incidence, likely origins, and mechanisms for cell lineage compartmentalization, Prenat. Diagn., 16, 511-524.
-
(1996)
Prenat. Diagn.
, vol.16
, pp. 511-524
-
-
Wolstenholme, J.1
-
44
-
-
0028792084
-
Elevated alpha-fetoprotein and human chorionic gonadotropin as a marker for placental trisomy 16 in the second trimester
-
Zimmerman, R., Lauper, U., Streicher, A., Huch, R., Huch, A. (1995). Elevated alpha-fetoprotein and human chorionic gonadotropin as a marker for placental trisomy 16 in the second trimester, Prenat. Diagn., 15, 1121-1124.
-
(1995)
Prenat. Diagn.
, vol.15
, pp. 1121-1124
-
-
Zimmerman, R.1
Lauper, U.2
Streicher, A.3
Huch, R.4
Huch, A.5
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