-
1
-
-
71949118947
-
Recurrence risks for trisomies 13, 18, and 21
-
De Souza E, Halliday J, Chan A, Bower C, Morris JK. 2009. Recurrence risks for trisomies 13, 18, and 21. Am J Med Genet Part A 149A: 2716- 2722.
-
(2009)
Am J Med Genet Part A
, vol.149 A
, pp. 2716-2722
-
-
De Souza, E.1
Halliday, J.2
Chan, A.3
Bower, C.4
Morris, J.K.5
-
3
-
-
0029858069
-
Sex ratio in normal and disomic sperm: Evidence that the extra chromosome 21 preferentially segregates with the Y chromosome
-
Griffin DK, Abruzzo MA, Millie EA, Feingold E, Hassold TJ. 1996. Sex ratio in normal and disomic sperm: Evidence that the extra chromosome 21 preferentially segregates with the Y chromosome. Am J Hum Genet 59: 1108- 1113.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 1108-1113
-
-
Griffin, D.K.1
Abruzzo, M.A.2
Millie, E.A.3
Feingold, E.4
Hassold, T.J.5
-
4
-
-
38449087657
-
The origin of human aneuploidy: Where we have been, where we are going
-
Hassold T, Hall H, Hunt P. 2007. The origin of human aneuploidy: Where we have been, where we are going. Hum Mol Genet 16: R203- R208.
-
(2007)
Hum Mol Genet
, vol.16
-
-
Hassold, T.1
Hall, H.2
Hunt, P.3
-
5
-
-
15744365616
-
Epidemiology of double aneuploidies involving chromosome 21 and the sex chromosomes
-
Kovaleva NV, Mutton DE. 2005. Epidemiology of double aneuploidies involving chromosome 21 and the sex chromosomes. Am J Med Genet Part A 134A: 24- 32.
-
(2005)
Am J Med Genet Part A
, vol.134 A
, pp. 24-32
-
-
Kovaleva, N.V.1
Mutton, D.E.2
-
6
-
-
84859967278
-
-
Cytological and epidemiological findings in Down syndrome: England and Wales 1989-2009. in press.
-
Morris JK, Alberman E, Mutton D, Jacobs P. Cytological and epidemiological findings in Down syndrome: England and Wales 1989-2009. in press.
-
-
-
Morris, J.K.1
Alberman, E.2
Mutton, D.3
Jacobs, P.4
-
7
-
-
29544451770
-
Recurrences of free trisomy 21: Analysis of data from the National Down Syndrome Cytogenetic Register
-
Morris JK, Mutton DE, Alberman E. 2005. Recurrences of free trisomy 21: Analysis of data from the National Down Syndrome Cytogenetic Register. Prenat Diagn 25: 1120- 1128.
-
(2005)
Prenat Diagn
, vol.25
, pp. 1120-1128
-
-
Morris, J.K.1
Mutton, D.E.2
Alberman, E.3
-
8
-
-
41849137305
-
The risk of fetal loss following a prenatal diagnosis of trisomy 13 or trisomy 18
-
PubMed PMID: 18361449.
-
Morris JK, Savva GM. 2008. The risk of fetal loss following a prenatal diagnosis of trisomy 13 or trisomy 18. Am J Med Genet Part A 146A: 827- 832. PubMed PMID: 18361449.
-
(2008)
Am J Med Genet Part A
, vol.146 A
, pp. 827-832
-
-
Morris, J.K.1
Savva, G.M.2
-
9
-
-
0029917626
-
Cytogenetic and epidemiological findings in Down syndrome, England and Wales 1989 to 1993. National Down Syndrome Cytogenetic Register and the Association of Clinical Cytogeneticists
-
Mutton D, Alberman E, Hook EB. 1996. Cytogenetic and epidemiological findings in Down syndrome, England and Wales 1989 to 1993. National Down Syndrome Cytogenetic Register and the Association of Clinical Cytogeneticists. J Med Genet 33: 387- 394.
-
(1996)
J Med Genet
, vol.33
, pp. 387-394
-
-
Mutton, D.1
Alberman, E.2
Hook, E.B.3
-
10
-
-
84859973760
-
-
NDSCR. Annual reports.
-
NDSCR. Annual reports.
-
-
-
-
11
-
-
84859944361
-
Ascertainment and accuracy of Down syndrome cases reported in congenital anomaly registers in England and Wales
-
Savvva GM, Morris JK. 2006. Ascertainment and accuracy of Down syndrome cases reported in congenital anomaly registers in England and Wales. Arch Dis Child Fetal Neonatal Ed 26: 499- 504.
-
(2006)
Arch Dis Child Fetal Neonatal Ed
, vol.26
, pp. 499-504
-
-
Savvva, G.M.1
Morris, J.K.2
-
12
-
-
75149173155
-
The maternal age-specific live birth prevalence of trisomies 13 and 18 compared to trisomy 21 (Down syndrome)
-
Savva GM, Walker K, Morris JK. 2010. The maternal age-specific live birth prevalence of trisomies 13 and 18 compared to trisomy 21 (Down syndrome). Prenat Diagn 30: 57- 64.
-
(2010)
Prenat Diagn
, vol.30
, pp. 57-64
-
-
Savva, G.M.1
Walker, K.2
Morris, J.K.3
-
13
-
-
0027980592
-
Non-disjunction of chromosome 21 in maternal meiosis I: Evidence for a maternal age-dependent mechanism involving reduced recombination
-
Sherman SL, Petersen MB, Freeman SB, Hersey J, Pettay D, Taft L, Frantzen M, Mikkelsen M, Hassold TJ. 1994. Non-disjunction of chromosome 21 in maternal meiosis I: Evidence for a maternal age-dependent mechanism involving reduced recombination. Hum Mol Genet 3: 1529- 1535.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1529-1535
-
-
Sherman, S.L.1
Petersen, M.B.2
Freeman, S.B.3
Hersey, J.4
Pettay, D.5
Taft, L.6
Frantzen, M.7
Mikkelsen, M.8
Hassold, T.J.9
-
14
-
-
0035253363
-
Maternal sex chromosome non-disjunction: Evidence for X chromosome-specific risk factors
-
Thomas NS, Ennis S, Sharp AJ, Durkie M, Hassold TJ, Collins AR, Jacobs PA. 2001. Maternal sex chromosome non-disjunction: Evidence for X chromosome-specific risk factors. Hum Mol Genet 10: 243- 250.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 243-250
-
-
Thomas, N.S.1
Ennis, S.2
Sharp, A.J.3
Durkie, M.4
Hassold, T.J.5
Collins, A.R.6
Jacobs, P.A.7
-
15
-
-
4143106805
-
Trisomy rec urrence: A reconsideration based on North American data
-
Warburton D, Dallaire L, Thangavelu M, Ross L, Levin B, Kline J. 2004. Trisomy rec urrence: A reconsideration based on North American data. Am J Hum Genet 75: 376- 385.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 376-385
-
-
Warburton, D.1
Dallaire, L.2
Thangavelu, M.3
Ross, L.4
Levin, B.5
Kline, J.6
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