-
1
-
-
0025981145
-
Predivision in human oocytes at meiosis I: A mechanism for trisomy formation in man
-
Angell RR (1991) Predivision in human oocytes at meiosis I: a mechanism for trisomy formation in man. Hum Genet 86:383-387
-
(1991)
Hum Genet
, vol.86
, pp. 383-387
-
-
Angell, R.R.1
-
2
-
-
0028910079
-
Meiosis I in human oocytes
-
Angell RR (1995) Meiosis I in human oocytes. Cytogenet Cell Genet 69:266-272
-
(1995)
Cytogenet Cell Genet
, vol.69
, pp. 266-272
-
-
Angell, R.R.1
-
3
-
-
0030845881
-
First meiotic division nondisjunction in human oocytes
-
Angell R (1997) First meiotic division nondisjunction in human oocytes. Am J Hum Genet 61:23-32
-
(1997)
Am J Hum Genet
, vol.61
, pp. 23-32
-
-
Angell, R.1
-
4
-
-
0027141914
-
First meiotic division abnormalities in human oocytes: Mechanism of trisomy formation
-
Angell RR, Xian J, Keith J, Ledger W, Baird DT (1994) First meiotic division abnormalities in human oocytes: mechanism of trisomy formation. Cytogenet Cell Genet 65:194-202
-
(1994)
Cytogenet Cell Genet
, vol.65
, pp. 194-202
-
-
Angell, R.R.1
Xian, J.2
Keith, J.3
Ledger, W.4
Baird, D.T.5
-
5
-
-
0027447719
-
Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age
-
Antonarakis SE, Avramopoulos D, Blouin J-L, Talbot CC Jr, Schinzel AA (1993) Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age. Nat Genet 3:146-150
-
(1993)
Nat Genet
, vol.3
, pp. 146-150
-
-
Antonarakis, S.E.1
Avramopoulos, D.2
Blouin, J.-L.3
Talbot C.C., Jr.4
Schinzel, A.A.5
-
7
-
-
0018392825
-
Cloning of the human satellite III DNA: Different components are on different chromosomes
-
Cooke HJ, Hindley J (1979) Cloning of the human satellite III DNA: different components are on different chromosomes. Nucleic Acids Res 6:3177-3179
-
(1979)
Nucleic Acids Res
, vol.6
, pp. 3177-3179
-
-
Cooke, H.J.1
Hindley, J.2
-
8
-
-
0032971825
-
A trisomic germ cell line and precocious chromatid separation leads to recurrent trisomy 21 conception
-
Cozzi J, Conn CM, Harper JC, Winston RML, Delhanty JDA (1999) A trisomic germ cell line and precocious chromatid separation leads to recurrent trisomy 21 conception. Hum Genet 104:23-28
-
(1999)
Hum Genet
, vol.104
, pp. 23-28
-
-
Cozzi, J.1
Conn, C.M.2
Harper, J.C.3
Winston, R.M.L.4
Delhanty, J.D.A.5
-
9
-
-
0029997093
-
Association between nondisjunction and maternal age in meiosis-1 in human oocytes
-
Dailey T, Dall B, Cohen J, Munne S (1996) Association between nondisjunction and maternal age in meiosis-1 in human oocytes. Am J Genet 59:176-184
-
(1996)
Am J Genet
, vol.59
, pp. 176-184
-
-
Dailey, T.1
Dall, B.2
Cohen, J.3
Munne, S.4
-
10
-
-
0031009264
-
Multicolour FISH detects frequent chromosomal mosaicism and chaotic division in normal preimplantation embryos from fertile patients
-
Delhanty JDA, Harper J, Ao A, Handyside AH, Winston RML (1997) Multicolour FISH detects frequent chromosomal mosaicism and chaotic division in normal preimplantation embryos from fertile patients. Hum Genet 99:755-760
-
(1997)
Hum Genet
, vol.99
, pp. 755-760
-
-
Delhanty, J.D.A.1
Harper, J.2
Ao, A.3
Handyside, A.H.4
Winston, R.M.L.5
-
11
-
-
0022587147
-
Two subsets of human alphoid repetitive DNA show distinct preferential localisation in the pericentric regions of chromosomes 13, 18 and 21
-
Devilee P, Cremer T, Slagboom P, Bakker E, Scholl HP, Hager HD, Stevenson AF, Cornelisse CJ, Pearson PL (1986) Two subsets of human alphoid repetitive DNA show distinct preferential localisation 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.7
Cornelisse, C.J.8
Pearson, P.L.9
-
12
-
-
0030024592
-
Detection of aneuploidy in human oocytes and corresponding first polar bodies by fluorescent in situ hybridization
-
Dyban A, Freidine M, Severova E, Cieslak J, Ivakhnenko V, Verlinsky Y (1996) Detection of aneuploidy in human oocytes and corresponding first polar bodies by fluorescent in situ hybridization. J Assist Reprod Genet 13:7.3-78
-
(1996)
J Assist Reprod Genet
, vol.13
, pp. 73-78
-
-
Dyban, A.1
Freidine, M.2
Severova, E.3
Cieslak, J.4
Ivakhnenko, V.5
Verlinsky, Y.6
-
13
-
-
0028907505
-
Trisomy 18: Studies of the parent and cell division of origin and the effect of aberrant recombination on nondisjunction
-
Fisher JM, Harvey JF, Morton NE, Jacobs PA (1995) Trisomy 18: studies of the parent and cell division of origin and the effect of aberrant recombination on nondisjunction. Am J Hum Genet 56:669-675
-
(1995)
Am J Hum Genet
, vol.56
, pp. 669-675
-
-
Fisher, J.M.1
Harvey, J.F.2
Morton, N.E.3
Jacobs, P.A.4
-
14
-
-
0024801180
-
Chromosome-specific alpha satellite DNA from the centromere of human chromosome 16
-
Greig GM, England SB, Bedford HM, Willard HF (1989) Chromosome-specific alpha satellite DNA from the centromere of human chromosome 16. Am J Hum Genet 45:862-872
-
(1989)
Am J Hum Genet
, vol.45
, pp. 862-872
-
-
Greig, G.M.1
England, S.B.2
Bedford, H.M.3
Willard, H.F.4
-
15
-
-
0019198839
-
A cytogenetic study of 1000 spontaneous abortions
-
Hassold T, Chen N, Funkhouser J, Jooss T, Manuel B, Matsuura J, Matsuyama A, Wilson C, Yamane JA, Jacobs PA (1980) A cytogenetic study of 1000 spontaneous abortions. Ann Hum Genet 44:151-178
-
(1980)
Ann Hum Genet
, vol.44
, pp. 151-178
-
-
Hassold, T.1
Chen, N.2
Funkhouser, J.3
Jooss, T.4
Manuel, B.5
Matsuura, J.6
Matsuyama, A.7
Wilson, C.8
Yamane, J.A.9
Jacobs, P.A.10
-
16
-
-
0029118422
-
Recombination and maternal-age dependent nondisjunction: Molecular studies of trisomy 16
-
Hassold T, Merrill M, Adkins K, Freeman S, Sherman S (1995) Recombination and maternal-age dependent nondisjunction: 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
-
17
-
-
0031869212
-
Cytogenetic and molecular studies of four couples with multiple trisomy 21 pregnancies
-
James RS, Ellis K, Pettay D, Jacobs PA (1998) Cytogenetic and molecular studies of four couples with multiple trisomy 21 pregnancies. Eur J Hum Genet 6:207-212
-
(1998)
Eur J Hum Genet
, vol.6
, pp. 207-212
-
-
James, R.S.1
Ellis, K.2
Pettay, D.3
Jacobs, P.A.4
-
18
-
-
0028196734
-
The chromosome constitution of human preimplantation embryos fertilized in vitro
-
Jamieson M E, Coutts JRT, Connor JM (1994) The chromosome constitution of human preimplantation embryos fertilized in vitro. Hum Reprod 9:709-715
-
(1994)
Hum Reprod
, vol.9
, pp. 709-715
-
-
Jamieson, M.E.1
Coutts, J.R.T.2
Connor, J.M.3
-
19
-
-
0027417385
-
Chromosome analysis of unfertilised human oocytes prepared by a gradual fixation-air drying method
-
Kamiguchi Y, Rosenbusch B, Sterizk K, Mikamo K (1993) Chromosome analysis of unfertilised human oocytes prepared by a gradual fixation-air drying method. Hum Genet 90:533-541
-
(1993)
Hum Genet
, vol.90
, pp. 533-541
-
-
Kamiguchi, Y.1
Rosenbusch, B.2
Sterizk, K.3
Mikamo, K.4
-
21
-
-
0031425426
-
Lack of checkpoint control at the metaphase/anaphase transition: A mechanism of meiotic nondisjunction in mammalian females
-
LeMaire-Adkins R, Radke K, Hunt PA (1997) Lack of checkpoint control at the metaphase/anaphase transition: a mechanism of meiotic nondisjunction in mammalian females. J Cell Biol 139: 1611-1619
-
(1997)
J Cell Biol
, vol.139
, pp. 1611-1619
-
-
LeMaire-Adkins, R.1
Radke, K.2
Hunt, P.A.3
-
22
-
-
0031706113
-
Chromosome identification in human oocytes and polar bodies by spectral karyotyping
-
Marquez C, Cohen J, Munne S (1998) Chromosome identification in human oocytes and polar bodies by spectral karyotyping. Cytogenet Cell Genet 81:254-258
-
(1998)
Cytogenet Cell Genet
, vol.81
, pp. 254-258
-
-
Marquez, C.1
Cohen, J.2
Munne, S.3
-
23
-
-
0025653494
-
Trisomy 21 mosaicism in gonads with unexpectedly high recurrence risks
-
Sachs ES, Jahoda MGJ, Los FJ, Pijpers L, Wladimiroff JW (1990) Trisomy 21 mosaicism in gonads with unexpectedly high recurrence risks. Am J Med Genet Suppl 7:186-188
-
(1990)
Am J Med Genet Suppl
, vol.7
, pp. 186-188
-
-
Sachs, E.S.1
Jahoda, M.G.J.2
Los, F.J.3
Pijpers, L.4
Wladimiroff, J.W.5
-
24
-
-
0000330352
-
An air drying method for chromosome preparation from mouse eggs
-
Tarkowski AK (1966) An air drying method for chromosome preparation from mouse eggs. Cytogenetics 5:394-400
-
(1966)
Cytogenetics
, vol.5
, pp. 394-400
-
-
Tarkowski, A.K.1
-
25
-
-
0032903719
-
Prevention of age-related aneuploidies by polar body testing of oocytes
-
Verlinsky Y, Cieslak J, Ivakhnenko V, Evsikov S, Wolf G, White M, Lifchez A, Kaplan B, Moise J, Valle J, Ginsberg N, Strom C, Kuliev A (1999) Prevention of age-related aneuploidies by polar body testing of oocytes. J Assist Reprod Genet 16:165-169
-
(1999)
J Assist Reprod Genet
, vol.16
, pp. 165-169
-
-
Verlinsky, Y.1
Cieslak, J.2
Ivakhnenko, V.3
Evsikov, S.4
Wolf, G.5
White, M.6
Lifchez, A.7
Kaplan, B.8
Moise, J.9
Valle, J.10
Ginsberg, N.11
Strom, C.12
Kuliev, A.13
-
26
-
-
0008229810
-
Isolation and characterisation of a major tandem repeat family from the human X chromosome
-
Willard HF, Smith KD, Sutherland J (1983) Isolation and characterisation of a major tandem repeat family from the human X chromosome. Nucleic Acids Res 19:3237-3241
-
(1983)
Nucleic Acids Res
, vol.19
, pp. 3237-3241
-
-
Willard, H.F.1
Smith, K.D.2
Sutherland, J.3
-
27
-
-
0026573160
-
Cytogenetics of human oocytes, zygotes and embryos after in vitro fertilization
-
Zenzes MT, Casper RF (1992) Cytogenetics of human oocytes, zygotes and embryos after in vitro fertilization. Hum Genet 88: 367-375
-
(1992)
Hum Genet
, vol.88
, pp. 367-375
-
-
Zenzes, M.T.1
Casper, R.F.2
|