-
2
-
-
0029962180
-
Delineation of a clinical syndrome caused by mosaic trisomy 15
-
Bühler EM, Bienz G, Straumann E, Bosch N. 1996. Delineation of a clinical syndrome caused by mosaic trisomy 15. Am J Med Genet 62:109-112.
-
(1996)
Am J Med Genet
, vol.62
, pp. 109-112
-
-
Bühler, E.M.1
Bienz, G.2
Straumann, E.3
Bosch, N.4
-
3
-
-
84881192326
-
Retrospective analysis of outcomes after IVF using an aneuploidy risk model derived from time-lapse imaging without PGS
-
Campbell A, Fishel S, Bowman N, Duffy S, Sedler M, Thornton S. 2013. Retrospective analysis of outcomes after IVF using an aneuploidy risk model derived from time-lapse imaging without PGS. Reprod Biomed Online 27:140-146.
-
(2013)
Reprod Biomed Online
, vol.27
, pp. 140-146
-
-
Campbell, A.1
Fishel, S.2
Bowman, N.3
Duffy, S.4
Sedler, M.5
Thornton, S.6
-
4
-
-
0019798833
-
A case of trisomy of chromosome 15
-
Coldwell S, Fitzgerald B, Semmens JM, Ede R, Bateman C. 1981. A case of trisomy of chromosome 15. J Med Genet 18:146-148.
-
(1981)
J Med Genet
, vol.18
, pp. 146-148
-
-
Coldwell, S.1
Fitzgerald, B.2
Semmens, J.M.3
Ede, R.4
Bateman, C.5
-
6
-
-
0032932423
-
Trisomy 15 CPM: probable origins, pregnancy outcome and risk of fetal UPD: European Collaborative Research on Mosaicism in CVS (EUCROMIC)
-
1999. Trisomy 15 CPM: probable origins, pregnancy outcome and risk of fetal UPD: European Collaborative Research on Mosaicism in CVS (EUCROMIC). Prenat Diagn 19:29-35.
-
(1999)
Prenat Diagn
, vol.19
, pp. 29-35
-
-
-
7
-
-
0027321155
-
A specific phenotype associated with trisomy 15 mosaicism
-
Fryns JP, Kleczkowska A, Lagae L, Kenis H, van den Berghe H. 1993. A specific phenotype associated with trisomy 15 mosaicism. Ann Genet 36:129-131.
-
(1993)
Ann Genet
, vol.36
, pp. 129-131
-
-
Fryns, J.P.1
Kleczkowska, A.2
Lagae, L.3
Kenis, H.4
van den Berghe, H.5
-
10
-
-
84888243273
-
An infant with trisomy 15 mosaicism
-
Isikay S, Carman KB. 2013. An infant with trisomy 15 mosaicism. Clin Dysmorphol 22:172-174.
-
(2013)
Clin Dysmorphol
, vol.22
, pp. 172-174
-
-
Isikay, S.1
Carman, K.B.2
-
11
-
-
14844347444
-
Mosaic trisomy 15 in a short girl with hemihypertrophy and mental retardation
-
Knauer-Fischer SA, Richter-Unruh A, Albrecht B, Gillessen-Kaesbach G, Hauffa BP. 2004. Mosaic trisomy 15 in a short girl with hemihypertrophy and mental retardation. Clin Dysmorphol 13:183-186.
-
(2004)
Clin Dysmorphol
, vol.13
, pp. 183-186
-
-
Knauer-Fischer, S.A.1
Richter-Unruh, A.2
Albrecht, B.3
Gillessen-Kaesbach, G.4
Hauffa, B.P.5
-
12
-
-
26244452194
-
Frequency and distribution of chromosome abnormalities in human oocytes
-
Kuliev A, Cieslak J, Verlinsky Y. 2005. Frequency and distribution of chromosome abnormalities in human oocytes. Cytogenet Genome Res 111:193-198.
-
(2005)
Cytogenet Genome Res
, vol.111
, pp. 193-198
-
-
Kuliev, A.1
Cieslak, J.2
Verlinsky, Y.3
-
13
-
-
0025961506
-
Trisomy 15 associated with nonimmune hydrops
-
Kuller JA, Laifer SA. 1991. Trisomy 15 associated with nonimmune hydrops. Am J Perinatol 8:39-40.
-
(1991)
Am J Perinatol
, vol.8
, pp. 39-40
-
-
Kuller, J.A.1
Laifer, S.A.2
-
14
-
-
0026638252
-
Mosaic trisomy 15 found at amniocentesis
-
Lähdetie J, Lakkal T. 1992. Mosaic trisomy 15 found at amniocentesis. Prenat Diagn 12:551-552.
-
(1992)
Prenat Diagn
, vol.12
, pp. 551-552
-
-
Lähdetie, J.1
Lakkal, T.2
-
15
-
-
0030043609
-
Trisomy 15 mosaicism and uniparental disomy (UPD) in a liveborn infant
-
Milunsky JM, Wyandt HE, Huang XL, Kang XZ, Elias ER, Milunsky A. 1996. Trisomy 15 mosaicism and uniparental disomy (UPD) in a liveborn infant. Am J Med Genet 61:269-273.
-
(1996)
Am J Med Genet
, vol.61
, pp. 269-273
-
-
Milunsky, J.M.1
Wyandt, H.E.2
Huang, X.L.3
Kang, X.Z.4
Elias, E.R.5
Milunsky, A.6
-
16
-
-
0034640677
-
Third Prader-Willi syndrome phenotype due to maternal uniparental disomy 15 with trisomy 15
-
Olander E, Stamnerg J, Steinberg L, Wulfsberg EA. 2000. Third Prader-Willi syndrome phenotype due to maternal uniparental disomy 15 with trisomy 15. Am J Med Genet 93:215-218.
-
(2000)
Am J Med Genet
, vol.93
, pp. 215-218
-
-
Olander, E.1
Stamnerg, J.2
Steinberg, L.3
Wulfsberg, E.A.4
-
17
-
-
33745632137
-
Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): Implication for prenatal diagnosis
-
Prontera P, Buldrini B, Aiello V, Gruppioni R, Bonfatti A, Venti G, Ferlini A, Sensi A, Calzolari E, Donti E. 2006. Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): Implication for prenatal diagnosis. Prenat Diagn 26:571-576.
-
(2006)
Prenat Diagn
, vol.26
, pp. 571-576
-
-
Prontera, P.1
Buldrini, B.2
Aiello, V.3
Gruppioni, R.4
Bonfatti, A.5
Venti, G.6
Ferlini, A.7
Sensi, A.8
Calzolari, E.9
Donti, E.10
-
18
-
-
14744269525
-
Severe intrauterine growth restriction and trisomy 15 confined placental mosaicism: A case report and review of literature
-
Redaelli S, Sala E, Roncaglia N, Colombo C, Crosti F, Villa N, Tagliabue P, Cappellini A, Dalpra L. 2005. Severe intrauterine growth restriction and trisomy 15 confined placental mosaicism: A case report and review of literature. Prenat Diagn 25:140-147.
-
(2005)
Prenat Diagn
, vol.25
, pp. 140-147
-
-
Redaelli, S.1
Sala, E.2
Roncaglia, N.3
Colombo, C.4
Crosti, F.5
Villa, N.6
Tagliabue, P.7
Cappellini, A.8
Dalpra, L.9
-
20
-
-
0002722022
-
Trisomy 15 in a mosaic, doubly aneuploid two year old
-
suppl) .
-
Stallard R, Sommer A. 1989. Trisomy 15 in a mosaic, doubly aneuploid two year old. Am J Hum Genet 45: (suppl) A92.
-
(1989)
Am J Hum Genet
, vol.45
, pp. A92
-
-
Stallard, R.1
Sommer, A.2
-
21
-
-
0027937004
-
Nondisjunction of human acrocentric chromosomes. Studies of 432 trisomic fetuses and liveborns
-
Zaragoza MV, Jacobs PA, James RS, Rogan P, Sherman S, Hassold T. 1994. Nondisjunction of human acrocentric chromosomes. Studies of 432 trisomic fetuses and liveborns. Hum Genet 94:411-417.
-
(1994)
Hum Genet
, vol.94
, pp. 411-417
-
-
Zaragoza, M.V.1
Jacobs, P.A.2
James, R.S.3
Rogan, P.4
Sherman, S.5
Hassold, T.6
-
22
-
-
0031959602
-
Prenatal diagnosis of low level trisomy 15 mosaicism: Review of the literature
-
Zaslav AL, Fallet S, Brown S, Ebert R, Fleischer A, Valderama E, Fox JE. 1998. Prenatal diagnosis of low level trisomy 15 mosaicism: Review of the literature. Clin Genet 53:286-292.
-
(1998)
Clin Genet
, vol.53
, pp. 286-292
-
-
Zaslav, A.L.1
Fallet, S.2
Brown, S.3
Ebert, R.4
Fleischer, A.5
Valderama, E.6
Fox, J.E.7
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