-
3
-
-
0002931375
-
Le mongolism. Premier exemple d'aberration autosomique humaine
-
Lejeune J. Le Mongolism. Premier exemple d'aberration autosomique humaine. Ann Genet 1959: 1: 41 49.
-
(1959)
Ann Genet
, vol.1
, pp. 41-49
-
-
Lejeune, J.1
-
4
-
-
10544226872
-
Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal MI and MII
-
Lamb N, Freeman S, Savage-Austin A et al. Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal MI and MII. Nat Genet 1996: 14: 400 405.
-
(1996)
Nat Genet
, vol.14
, pp. 400-405
-
-
Lamb, N.1
Freeman, S.2
Savage-Austin, A.3
-
5
-
-
0030058258
-
Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of the chromosomal error: A population-based study
-
Yoon PW, Freeman SB, Sherman SL et al. Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of the chromosomal error: a population-based study. Am J Hum Genet 1996: 58: 628 633.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 628-633
-
-
Yoon, P.W.1
Freeman, S.B.2
Sherman, S.L.3
-
6
-
-
0030767256
-
Meiotic chromosomes: It takes two to tango
-
Roeder GS. Meiotic chromosomes: it takes two to tango. Genes Dev 1997: 11: 2600 2621.
-
(1997)
Genes Dev
, vol.11
, pp. 2600-2621
-
-
Roeder, G.S.1
-
7
-
-
0023236677
-
Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome
-
Warren AC, Chakravarti A, Wong C et al. Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome. Science 1987: 237: 652 654.
-
(1987)
Science
, vol.237
, pp. 652-654
-
-
Warren, A.C.1
Chakravarti, A.2
Wong, C.3
-
8
-
-
0026334334
-
XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region
-
Hassold TJ. Sherman SL, Pettay D, Page DC, Jacobs PA. XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region. Am J Hum Genet 1991: 49: 253-260.
-
(1991)
Am J Hum Genet
, vol.49
, pp. 253-260
-
-
Hassold, T.J.1
Sherman, S.L.2
Pettay, D.3
Page, D.C.4
Jacobs, P.A.5
-
9
-
-
0028030585
-
The origin of 47,XXY and 47,XXX aneuploidy: Heterogeneous mechanisms and role of aberrant recombination
-
MacDonald M, Hassold T, Harvey J, Wang LH, Morton NE, Jacobs P, The origin of 47,XXY and 47,XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination. Hum Genet 1994: 3: 1365 1371.
-
(1994)
Hum Genet
, vol.3
, pp. 1365-1371
-
-
MacDonald, M.1
Hassold, T.2
Harvey, J.3
Wang, L.H.4
Morton, N.E.5
Jacobs, P.6
-
10
-
-
7144260410
-
Maternal meiosis I nondisjunction of chromosome 15: Dependence of the maternal age effect on level of recombination
-
Robinson W, Kuchinka B, Bernasconi F et al. Maternal meiosis I nondisjunction of chromosome 15: dependence of the maternal age effect on level of recombination. Hum Mol Genet 1998: 7: 1011 1020.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 1011-1020
-
-
Robinson, W.1
Kuchinka, B.2
Bernasconi, F.3
-
11
-
-
0029118422
-
Recombination and maternal-age dependent nondisjunction: Molecular studies of trisomy 16
-
Hassold T, Merrill M, Adkins K, Freeman S, Sherman S. Recombination and maternal-age dependent nondisjunction: molecular studies of trisomy 16. Am J Hum Genet 1995: 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
-
13
-
-
9844220844
-
Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21
-
Lamb N, Feingold E, Savage-Austin A et al. Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21. Hum Mol Genet 1997: 6: 1391 1399.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1391-1399
-
-
Lamb, N.1
Feingold, E.2
Savage-Austin, A.3
-
15
-
-
0026050710
-
The lethal(1)TW-6cs mutation in Drosophila melanogaster is a dominant allele of nod and is associated with a single base pair change in the putative ATP-binding domain
-
Rasooly RS, New CM, Zhang P, Hawley RS, Baker BS, The lethal(1)TW-6cs mutation in Drosophila melanogaster is a dominant allele of nod and is associated with a single base pair change in the putative ATP-binding domain. Genetics 1991: 129: 409 422.
-
(1991)
Genetics
, vol.129
, pp. 409-422
-
-
Rasooly, R.S.1
New, C.M.2
Zhang, P.3
Hawley, R.S.4
Baker, B.S.5
-
16
-
-
0031972533
-
Chromosome segregation during meiosis: Building an unambivalent bivalent
-
Moore DP, Orr-Weaver TL, Chromosome segregation during meiosis: building an unambivalent bivalent. Curr Top Dev Biol 1998: 37: 263 299.
-
(1998)
Curr Top Dev Biol
, vol.37
, pp. 263-299
-
-
Moore, D.P.1
Orr-Weaver, T.L.2
-
17
-
-
7344224406
-
Elucidating the mechanisms of paternal nondisjunction of chromosome 21 in humans
-
Savage A, Petersen M, Pettay D et al. Elucidating the mechanisms of paternal nondisjunction of chromosome 21 in humans. Hum Mol Genet 1998: 7: 1221-1227.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 1221-1227
-
-
Savage, A.1
Petersen, M.2
Pettay, D.3
-
18
-
-
0021906685
-
Maternal age specific rates of numerical chromosome abnormalities with special reference to trisomy
-
Hassold T, Chiu D. Maternal age specific rates of numerical chromosome abnormalities with special reference to trisomy. Hum Genet 1985: 70: 11-17.
-
(1985)
Hum Genet
, vol.70
, pp. 11-17
-
-
Hassold, T.1
Chiu, D.2
-
19
-
-
0003123842
-
Maternal age, paternal age, and human chromosome abnormality: Nature, magnitude, etiology, and mechanisms of effects
-
Dellarco V, Votek P, Hollaender A, eds. New York, NY: Plenum Press
-
Hook E. Maternal age, paternal age, and human chromosome abnormality: nature, magnitude, etiology, and mechanisms of effects. In: Dellarco V, Votek P, Hollaender A, eds. Aneuploidy: Etiology and Mechanisms. New York, NY: Plenum Press, 1985: 117-129.
-
(1985)
Aneuploidy: Etiology and Mechanisms
, pp. 117-129
-
-
Hook, E.1
-
20
-
-
0000049938
-
Chromosome abnormalities in human reproductive wastage
-
Hassold T. Chromosome abnormalities in human reproductive wastage. Trends Genet 1986: 2: 105-110.
-
(1986)
Trends Genet
, vol.2
, pp. 105-110
-
-
Hassold, T.1
-
21
-
-
0033086398
-
Risk factors for trisomy 21: Maternal cigarette smoking and oral contraceptive use in a population-based case-control study
-
Yang Q. Sherman S, Hassold T et al. Risk factors for trisomy 21: Maternal cigarette smoking and oral contraceptive use in a population-based case-control study. Genet Med 1999: 1: 80-88.
-
(1999)
Genet Med
, vol.1
, pp. 80-88
-
-
Yang, Q.1
Sherman, S.2
Hassold, T.3
|