-
1
-
-
0033214543
-
Screening for abnormalities of chromosomes X, Y, and 18 and for diploidy in spermatozoa from infertile men participating in an in vitro fertilization-intracytoplasmic sperm injection program
-
Aran B, Blanco J, Vidal F, Vendrell JM, Egozcue S, Barri PN, Egozcue J and Veiga A (1999) Screening for abnormalities of chromosomes X, Y, and 18 and for diploidy in spermatozoa from infertile men participating in an in vitro fertilization-intracytoplasmic sperm injection program Fertility and Sterility 72 696-701
-
(1999)
Fertility and Sterility
, vol.72
, pp. 696-701
-
-
Aran, B.1
Blanco, J.2
Vidal, F.3
Vendrell, J.M.4
Egozcue, S.5
Barri, P.N.6
Egozcue, J.7
Veiga, A.8
-
2
-
-
0033849378
-
Meiotic studies of a human male carrier of the common translocation, t(11;22), suggests postzygotic selection rather than preferential 3:1 Ml segregation as the cause of liveborn offspring with an unbalanced translocation
-
Armstrong SJ, Goldman AS, Speed RM and Hultén MA (2000) Meiotic studies of a human male carrier of the common translocation, t(11;22), suggests postzygotic selection rather than preferential 3:1 Ml segregation as the cause of liveborn offspring with an unbalanced translocation American Journal of Human Genetics 67 601-609
-
(2000)
American Journal of Human Genetics
, vol.67
, pp. 601-609
-
-
Armstrong, S.J.1
Goldman, A.S.2
Speed, R.M.3
Hultén, M.A.4
-
3
-
-
0020560397
-
Chromosome segregation into the spermatozoa of two men heterozygous for different reciprocal translocations
-
Balkan W and Martin RH (1983) Chromosome segregation into the spermatozoa of two men heterozygous for different reciprocal translocations Human Genetics 63 345-348
-
(1983)
Human Genetics
, vol.63
, pp. 345-348
-
-
Balkan, W.1
Martin, R.H.2
-
4
-
-
0032892314
-
Intracytoplasmic sperm injection pregnancy with trisomy 20p and monosomy 22q in a newborn resulting from a balanced paternal translocation
-
Belin V, Farhat M and Monset-Couchard M (1999) Intracytoplasmic sperm injection pregnancy with trisomy 20p and monosomy 22q in a newborn resulting from a balanced paternal translocation Biology of the Neonate 75 398-401
-
(1999)
Biology of the Neonate
, vol.75
, pp. 398-401
-
-
Belin, V.1
Farhat, M.2
Monset-Couchard, M.3
-
5
-
-
0023944147
-
Sperm chromosome complements in a 47,XYY male
-
Benet J and Martin R (1988) Sperm chromosome complements in a 47,XYY male Human Genetics 78 313-315
-
(1988)
Human Genetics
, vol.78
, pp. 313-315
-
-
Benet, J.1
Martin, R.2
-
6
-
-
0031133236
-
Comparison of gonosomal aneuploidy in spermatozoa of normal fertile men and those with severe male factor detected by in situ hybridization
-
Bernardini L, Martini E, Geraedts JP, Hopman AH, Lanteri S, Conte N and Capitanio GL (1997) Comparison of gonosomal aneuploidy in spermatozoa of normal fertile men and those with severe male factor detected by in situ hybridization Molecular Human Reproduction 3 431-438
-
(1997)
Molecular Human Reproduction
, vol.3
, pp. 431-438
-
-
Bernardini, L.1
Martini, E.2
Geraedts, J.P.3
Hopman, A.H.4
Lanteri, S.5
Conte, N.6
Capitanio, G.L.7
-
7
-
-
0032422605
-
Study of aneuploidy in normal and abnormal germ cells from semen of fertile and infertile men
-
Bernardini L, Borini A, Preti S, Conte N, Flamigni C, Capitanio GL and Venturini PL (1998) Study of aneuploidy in normal and abnormal germ cells from semen of fertile and infertile men Human Reproduction 13 3406-3413
-
(1998)
Human Reproduction
, vol.13
, pp. 3406-3413
-
-
Bernardini, L.1
Borini, A.2
Preti, S.3
Conte, N.4
Flamigni, C.5
Capitanio, G.L.6
Venturini, P.L.7
-
8
-
-
0033984412
-
Fluorescence in situ hybridization of sex chromosomes in spermatozoa and spare preimplantation embryos of a Klinefelter 46,XY/47,XXY male
-
Bielanska M, Tan SL and Ao A (2000) Fluorescence in situ hybridization of sex chromosomes in spermatozoa and spare preimplantation embryos of a Klinefelter 46,XY/47,XXY male Human Reproduction 15 440-444
-
(2000)
Human Reproduction
, vol.15
, pp. 440-444
-
-
Bielanska, M.1
Tan, S.L.2
Ao, A.3
-
9
-
-
0032454305
-
FISH on sperm heads allows the analysis of chromosome segregation and interchromosomal effects in carriers of structural rearrangements: Results in a translocation carrier, t(5;8)(q33;q13)
-
Blanco J, Egozcue J, Clusellas N and Vidal F (1998) FISH on sperm heads allows the analysis of chromosome segregation and interchromosomal effects in carriers of structural rearrangements: results in a translocation carrier, t(5;8)(q33;q13) Cytogenetics and Cell Genetics 83 275-280
-
(1998)
Cytogenetics and Cell Genetics
, vol.83
, pp. 275-280
-
-
Blanco, J.1
Egozcue, J.2
Clusellas, N.3
Vidal, F.4
-
10
-
-
0034081889
-
Interchromosomal effects for chromosome 21 in carriers of structural chromosome reorganizations determined by flourescence in situ hybridization on sperm nuclei
-
Blanco J, Egozque J and Vidal F (2000) Interchromosomal effects for chromosome 21 in carriers of structural chromosome reorganizations determined by flourescence in situ hybridization on sperm nuclei Human Genetics 106 500-505
-
(2000)
Human Genetics
, vol.106
, pp. 500-505
-
-
Blanco, J.1
Egozque, J.2
Vidal, F.3
-
11
-
-
0031811730
-
Incidence of chromosomal aberrations in children born after assisted reproduction through intracytoplasmic sperm injections
-
Bonduelle M, Aytoz A, Van Assche E, Devroey P, Liebaers I and Van Steirteghem A (1998) Incidence of chromosomal aberrations in children born after assisted reproduction through intracytoplasmic sperm injections Human Reproduction 13 781-782
-
(1998)
Human Reproduction
, vol.13
, pp. 781-782
-
-
Bonduelle, M.1
Aytoz, A.2
Van Assche, E.3
Devroey, P.4
Liebaers, I.5
Van Steirteghem, A.6
-
12
-
-
0014506947
-
On XYY chromosome triplet. Its importance in psychiatry. Apropos of a case
-
Boucharlat J and Jalbert P (1969) On XYY chromosome triplet. Its importance in psychiatry. Apropos of a case Annales Medico-Psychologiques 1 793-797
-
(1969)
Annales Medico-psychologiques
, vol.1
, pp. 793-797
-
-
Boucharlat, J.1
Jalbert, P.2
-
13
-
-
0021229266
-
A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses
-
Boué H and Gallano P (1984) A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses Prenatal Diagnosis 4 45-67
-
(1984)
Prenatal Diagnosis
, vol.4
, pp. 45-67
-
-
Boué, H.1
Gallano, P.2
-
14
-
-
0030731505
-
Delivery of normal twins following the intracytoplasmic injection of spermatozoa from a patient with 47,XXY Klinefelter's syndrome
-
Bourne H, Stern K, Clarke G, Pertile M, Speirs A and Baker HW (1997) Delivery of normal twins following the intracytoplasmic injection of spermatozoa from a patient with 47,XXY Klinefelter's syndrome Human Reproduction 12 2447-2450
-
(1997)
Human Reproduction
, vol.12
, pp. 2447-2450
-
-
Bourne, H.1
Stern, K.2
Clarke, G.3
Pertile, M.4
Speirs, A.5
Baker, H.W.6
-
15
-
-
0032937465
-
Characterization of aneuploidy rates, protamine levels, ultrastructure, and functional ability of round-headed sperm from two siblings and implications for intracytoplasmic sperm injection
-
Carrell D, Emery BR and Liu L (1999) Characterization of aneuploidy rates, protamine levels, ultrastructure, and functional ability of round-headed sperm from two siblings and implications for intracytoplasmic sperm injection Fertility and Sterility 71 511-516
-
(1999)
Fertility and Sterility
, vol.71
, pp. 511-516
-
-
Carrell, D.1
Emery, B.R.2
Liu, L.3
-
16
-
-
0030024760
-
Increased incidence of hyperhaploid 24,XY spermatozoa detected by three-colour FISH in a 46,XY/47,XXY male
-
Chevret E, Rousseaux S, Monteil M, Usson Y, Cozzi J, Pelletier R and Sele B (1996) Increased incidence of hyperhaploid 24,XY spermatozoa detected by three-colour FISH in a 46,XY/47,XXY male Human Genetics 97 171-175
-
(1996)
Human Genetics
, vol.97
, pp. 171-175
-
-
Chevret, E.1
Rousseaux, S.2
Monteil, M.3
Usson, Y.4
Cozzi, J.5
Pelletier, R.6
Sele, B.7
-
17
-
-
0031058096
-
Meiotic behaviour of sex chromosomes investigated by three-colour FISH on 35 142 sperm nuclei from two 47, XYY males
-
Chevret E, Rousseaux S, Monteil M, Usson Y, Cozzi J, Pelletier R and Sele B (1997) Meiotic behaviour of sex chromosomes investigated by three-colour FISH on 35 142 sperm nuclei from two 47, XYY males Human Genetics 99 407-412
-
(1997)
Human Genetics
, vol.99
, pp. 407-412
-
-
Chevret, E.1
Rousseaux, S.2
Monteil, M.3
Usson, Y.4
Cozzi, J.5
Pelletier, R.6
Sele, B.7
-
18
-
-
0032987761
-
Cytogenetic analysis of sperm chromosomes and sperm nuclei in a male heterozygous for a reciprocal translocation t(5;7)(q21;q32) by in situ hybridization
-
Cifuentes P, Navarro J, Blanco J, Vidal F, Miguez L, Egozcue J and Benet J (1999) Cytogenetic analysis of sperm chromosomes and sperm nuclei in a male heterozygous for a reciprocal translocation t(5;7)(q21;q32) by in situ hybridization European Journal of Human Genetics 7 231-238
-
(1999)
European Journal of Human Genetics
, vol.7
, pp. 231-238
-
-
Cifuentes, P.1
Navarro, J.2
Blanco, J.3
Vidal, F.4
Miguez, L.5
Egozcue, J.6
Benet, J.7
-
19
-
-
0033168808
-
Incidence of sperm aneuploidy in relation to semen characteristics and assisted reproductive outcome
-
Colombero LT, Hariprashad JJ, Tsai MC, Rosenwaks Z and Palermo GD (1999) Incidence of sperm aneuploidy in relation to semen characteristics and assisted reproductive outcome Fertility and Sterility 72 90-96
-
(1999)
Fertility and Sterility
, vol.72
, pp. 90-96
-
-
Colombero, L.T.1
Hariprashad, J.J.2
Tsai, M.C.3
Rosenwaks, Z.4
Palermo, G.D.5
-
20
-
-
0033802569
-
Incidence of aneuploid spermatozoa from subfertile men: Selected with motility versus hemizona-bound
-
Dyk QV, Lanzendorf S, Kolm P, Hodgen GD and Mahony MC (2000) Incidence of aneuploid spermatozoa from subfertile men: selected with motility versus hemizona-bound Human Reproduction 15 1529-1536
-
(2000)
Human Reproduction
, vol.15
, pp. 1529-1536
-
-
Dyk, Q.V.1
Lanzendorf, S.2
Kolm, P.3
Hodgen, G.D.4
Mahony, M.C.5
-
21
-
-
0021058956
-
Meiotic studies in a series of 1100 infertile and sterile males
-
Egozcue I, Templado C, Vidal F, Navarro J, Morer-Fargas F and Marina S (1983) Meiotic studies in a series of 1100 infertile and sterile males Human Genetics 65 185-188
-
(1983)
Human Genetics
, vol.65
, pp. 185-188
-
-
Egozcue, I.1
Templado, C.2
Vidal, F.3
Navarro, J.4
Morer-Fargas, F.5
Marina, S.6
-
22
-
-
0033941370
-
Analysis of chromosome abnormalities in sperm and embryos from two 45,XY,t(13;14)(q10;q10) carriers
-
Escudero T, Lee M, Carrel D, Blanco J and Munne S (2000) Analysis of chromosome abnormalities in sperm and embryos from two 45,XY,t(13;14)(q10;q10) carriers Prenatal Diagnosis 20 599-602
-
(2000)
Prenatal Diagnosis
, vol.20
, pp. 599-602
-
-
Escudero, T.1
Lee, M.2
Carrel, D.3
Blanco, J.4
Munne, S.5
-
23
-
-
0030982686
-
The meiotic segregation pattern of a reciprocal translocation t(10;12)(q26.1;p13.3) by fluorescence in situ hybridization sperm analysis
-
Estop AM, Cieply KM and Aston CE (1997) The meiotic segregation pattern of a reciprocal translocation t(10;12)(q26.1;p13.3) by fluorescence in situ hybridization sperm analysis European Journal of Human Genetics 5 78-82
-
(1997)
European Journal of Human Genetics
, vol.5
, pp. 78-82
-
-
Estop, A.M.1
Cieply, K.M.2
Aston, C.E.3
-
24
-
-
0031906986
-
Meiotic products of a Klinefelter 47,XXY male as determined by sperm fluorescence in situ hybridization analysis
-
Estop AM, Munne S, Cieply KM, Vandermark KK, Lamb AN and Fisch H (1998a) Meiotic products of a Klinefelter 47,XXY male as determined by sperm fluorescence in situ hybridization analysis Human Reproduction 13 124-127
-
(1998)
Human Reproduction
, vol.13
, pp. 124-127
-
-
Estop, A.M.1
Munne, S.2
Cieply, K.M.3
Vandermark, K.K.4
Lamb, A.N.5
Fisch, H.6
-
25
-
-
0032453869
-
Meiotic products of two reciprocal translocations studied by multicolor fluorescence in situ hybridization
-
Estop AM, Cieply KM, Wakim A and Feingold E (1998b) Meiotic products of two reciprocal translocations studied by multicolor fluorescence in situ hybridization Cytogenetics and Cell Genetics 83 193-198
-
(1998)
Cytogenetics and Cell Genetics
, vol.83
, pp. 193-198
-
-
Estop, A.M.1
Cieply, K.M.2
Wakim, A.3
Feingold, E.4
-
26
-
-
0032994872
-
Multicolor fluorescence in situ hybridization analysis of the spermatozoa of a male heterozygous for a reciprocal translocation t(11;22)(q23;q11)
-
Estop AM, Cieply KM, Munne S and Feingold E (1999) Multicolor fluorescence in situ hybridization analysis of the spermatozoa of a male heterozygous for a reciprocal translocation t(11;22)(q23;q11) Human Genetics 104 412-417
-
(1999)
Human Genetics
, vol.104
, pp. 412-417
-
-
Estop, A.M.1
Cieply, K.M.2
Munne, S.3
Feingold, E.4
-
27
-
-
0034130679
-
Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies
-
Estop A, Cieply K, Munne S, Surt U, Wakim A and Feingold E (2000) Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies Human Genetics 106 517-524
-
(2000)
Human Genetics
, vol.106
, pp. 517-524
-
-
Estop, A.1
Cieply, K.2
Munne, S.3
Surt, U.4
Wakim, A.5
Feingold, E.6
-
28
-
-
0031922364
-
Increased rate of nondisjunction in sex cells derived from low-quality semen
-
Finkelstein S, Mukamel E, Yavetz H, Paz G and Avivi L (1998) Increased rate of nondisjunction in sex cells derived from low-quality semen Human Genetics 102 129-137
-
(1998)
Human Genetics
, vol.102
, pp. 129-137
-
-
Finkelstein, S.1
Mukamel, E.2
Yavetz, H.3
Paz, G.4
Avivi, L.5
-
29
-
-
0031737995
-
High incidence of sperm sex chromosomes aneuploidies in two patients with Klinefelter's syndrome
-
Foresta C, Galeazzi C, Bettella A, Stella M and Scandellari C (1998) High incidence of sperm sex chromosomes aneuploidies in two patients with Klinefelter's syndrome Journal of Clinical Endocrinology and Metabolism 83 203-205
-
(1998)
Journal of Clinical Endocrinology and Metabolism
, vol.83
, pp. 203-205
-
-
Foresta, C.1
Galeazzi, C.2
Bettella, A.3
Stella, M.4
Scandellari, C.5
-
30
-
-
0033305420
-
Analysis of meiosis in intratesticular germ cells from subjects affected by classic Klinefelter's syndrome
-
Foresta C, Galeazzi C, Bettella A, Marin P, Rossato M, Garolla A and Ferlin A (1999) Analysis of meiosis in intratesticular germ cells from subjects affected by classic Klinefelter's syndrome Journal of Clinical Endocrinology and Metabolism 84 3807-3810
-
(1999)
Journal of Clinical Endocrinology and Metabolism
, vol.84
, pp. 3807-3810
-
-
Foresta, C.1
Galeazzi, C.2
Bettella, A.3
Marin, P.4
Rossato, M.5
Garolla, A.6
Ferlin, A.7
-
31
-
-
0032945605
-
Sperm analysis in a subfertile male with a Y;16 translocation, using four-color FISH
-
Giltay JC, Kastrop PM, Tiemessen CH, van Inzen WG, Scheres JM and Pearson PL (1999) Sperm analysis in a subfertile male with a Y;16 translocation, using four-color FISH Cytogenetics and Cell Genetics 84 67-72
-
(1999)
Cytogenetics and Cell Genetics
, vol.84
, pp. 67-72
-
-
Giltay, J.C.1
Kastrop, P.M.2
Tiemessen, C.H.3
Van Inzen, W.G.4
Scheres, J.M.5
Pearson, P.L.6
-
32
-
-
0030840912
-
Analysis of structural and numerical chromosome abnormalities in sperm of normal men and carriers of constitutional chromosome aberrations: A review
-
* Guttenbach M, Engel W and Schmid M (1997a) Analysis of structural and numerical chromosome abnormalities in sperm of normal men and carriers of constitutional chromosome aberrations: a review Human Genetics 100 1-21
-
(1997)
Human Genetics
, vol.100
, pp. 1-21
-
-
Guttenbach, M.1
Engel, W.2
Schmid, M.3
-
33
-
-
0030896411
-
Segregation of sex chromosomes into sperm nuclei in a man with 47,XXY Klinefelter's karyotype: A FISH analysis
-
Guttenbach M, Michelmann HW, Hinney B, Engel W and Schmid M (1997b) Segregation of sex chromosomes into sperm nuclei in a man with 47,XXY Klinefelter's karyotype: a FISH analysis Human Genetics 99 474-477
-
(1997)
Human Genetics
, vol.99
, pp. 474-477
-
-
Guttenbach, M.1
Michelmann, H.W.2
Hinney, B.3
Engel, W.4
Schmid, M.5
-
34
-
-
0026334334
-
XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region
-
Hassold T, Sherman S, Pettay D, Page D and Jacobs P (1991) XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region American Journal of Human Genetics 49 253-260
-
(1991)
American Journal of Human Genetics
, vol.49
, pp. 253-260
-
-
Hassold, T.1
Sherman, S.2
Pettay, D.3
Page, D.4
Jacobs, P.5
-
35
-
-
0032734017
-
Analysis of segregation and aneuploidy in two reciprocal translocation carriers, t(3;9)(q26.2;q.32) and t(3;9)(p25;q32), by triple-color fluorescence in situ hybridization
-
Honda H, Miharu N, Ohashi Y, Honda N, Hara T and Ohama K (1999) Analysis of segregation and aneuploidy in two reciprocal translocation carriers, t(3;9)(q26.2;q.32) and t(3;9)(p25;q32), by triple-color fluorescence in situ hybridization Human Genetics 105 428-436
-
(1999)
Human Genetics
, vol.105
, pp. 428-436
-
-
Honda, H.1
Miharu, N.2
Ohashi, Y.3
Honda, N.4
Hara, T.5
Ohama, K.6
-
36
-
-
0034017618
-
Meiotic segregation analysis of a 14;21 Robertsonian translocation carrier by fluorescence in situ hybridization
-
Honda H, Miharu N, Samura O, He H and Ohama K (2000) Meiotic segregation analysis of a 14;21 Robertsonian translocation carrier by fluorescence in situ hybridization Human Genetics 106 188-193
-
(2000)
Human Genetics
, vol.106
, pp. 188-193
-
-
Honda, H.1
Miharu, N.2
Samura, O.3
He, H.4
Ohama, K.5
-
37
-
-
0014932069
-
Meiosis in XYY men
-
Hultén M (1970) Meiosis in XYY men Lancet 1 717-718
-
(1970)
Lancet
, vol.1
, pp. 717-718
-
-
Hultén, M.1
-
38
-
-
0015014003
-
Fluorescent evidence for spermatocytes with two Y chromosomes in an XYY male
-
Hultén M and Pearson PL (1971) Fluorescent evidence for spermatocytes with two Y chromosomes in an XYY male Annals of Human Genetics 34 273-276
-
(1971)
Annals of Human Genetics
, vol.34
, pp. 273-276
-
-
Hultén, M.1
Pearson, P.L.2
-
39
-
-
1842338715
-
Two cases of Robertsonian translocations in oligozoospermic males and their consequences for pregnancies induced by intracytoplasmic sperm injection
-
In't Veld PA, Weber RF, Los FJ, den Hollander N, Dhont M, Pieters MH and Van Hemel JO (1997) Two cases of Robertsonian translocations in oligozoospermic males and their consequences for pregnancies induced by intracytoplasmic sperm injection Human Reproduction 12 1642-1644
-
(1997)
Human Reproduction
, vol.12
, pp. 1642-1644
-
-
In't Veld, P.A.1
Weber, R.F.2
Los, F.J.3
Den Hollander, N.4
Dhont, M.5
Pieters, M.H.6
Van Hemel, J.O.7
-
40
-
-
0018953638
-
Reciprocal translocations: A way to predict the mode of imbalanced segregation by pachytene-diagram drawing
-
Jalbert P, Sele B and Jalbert H (1980) Reciprocal translocations: a way to predict the mode of imbalanced segregation by pachytene-diagram drawing Human Genetics 55 209-222
-
(1980)
Human Genetics
, vol.55
, pp. 209-222
-
-
Jalbert, P.1
Sele, B.2
Jalbert, H.3
-
41
-
-
0031698004
-
Genetic risks of intracytoplasmic sperm injection in the treatment of male infertility, recommendations for genetic counseling and screening
-
Johnson MD (1998) Genetic risks of intracytoplasmic sperm injection in the treatment of male infertility, recommendations for genetic counseling and screening Fertility and Sterility 70 397-411
-
(1998)
Fertility and Sterility
, vol.70
, pp. 397-411
-
-
Johnson, M.D.1
-
42
-
-
0023869499
-
Predictive value of abnormal sperm morphology in in vitro fertilization
-
Kruger TF, Acosta AA, Simmons KF, Swanson RJ, Matta JF and Oehninger S (1988) Predictive value of abnormal sperm morphology in in vitro fertilization Fertility and Sterility 49 112-117
-
(1988)
Fertility and Sterility
, vol.49
, pp. 112-117
-
-
Kruger, T.F.1
Acosta, A.A.2
Simmons, K.F.3
Swanson, R.J.4
Matta, J.F.5
Oehninger, S.6
-
43
-
-
0031892963
-
Genetic counselling in a patient with XXY/XXXY/XY mosaic Klinefelter's syndrome: Estimate of sex chromosome aberrations in sperm before intracytoplasmic sperm injection
-
Kruse R, Guttenbach M, Schartmann B, Schubert R, van der Ven H, Schmid M and Propping P (1998) Genetic counselling in a patient with XXY/XXXY/XY mosaic Klinefelter's syndrome: estimate of sex chromosome aberrations in sperm before intracytoplasmic sperm injection Fertility and Sterility 69 432-485
-
(1998)
Fertility and Sterility
, vol.69
, pp. 432-485
-
-
Kruse, R.1
Guttenbach, M.2
Schartmann, B.3
Schubert, R.4
Van Der Ven, H.5
Schmid, M.6
Propping, P.7
-
44
-
-
0030910324
-
Incidence of aneuploid spermatozoa among infertile men studied by multicolor fluorescence in situ hybridization
-
Lahdetie J, Saari N, Ajosenpaa-Saari M and Mykkanen J (1997) Incidence of aneuploid spermatozoa among infertile men studied by multicolor fluorescence in situ hybridization American Journal of Medical Genetics 71 115-121
-
(1997)
American Journal of Medical Genetics
, vol.71
, pp. 115-121
-
-
Lahdetie, J.1
Saari, N.2
Ajosenpaa-Saari, M.3
Mykkanen, J.4
-
45
-
-
0029838780
-
Analysis of chromosome constitution of human spermatozoa with normal and aberrant head morphologies after injection into mouse oocytes
-
Lee JD, Kamiguchi Y and Yanagimachi R (1996) Analysis of chromosome constitution of human spermatozoa with normal and aberrant head morphologies after injection into mouse oocytes Human Reproduction 11 1942-1946
-
(1996)
Human Reproduction
, vol.11
, pp. 1942-1946
-
-
Lee, J.D.1
Kamiguchi, Y.2
Yanagimachi, R.3
-
46
-
-
0032406655
-
Detection of numerical chromosome abnormalities in human spermatozoa by three-color fluorescence in situ hybridization
-
Li P and Hoshiai H (1998) Detection of numerical chromosome abnormalities in human spermatozoa by three-color fluorescence in situ hybridization Journal of Obstetrics and Gynaecological Research 24 385-392
-
(1998)
Journal of Obstetrics and Gynaecological Research
, vol.24
, pp. 385-392
-
-
Li, P.1
Hoshiai, H.2
-
47
-
-
0028823335
-
Sex chromosome abnormalities after intracytoplasmic sperm injection
-
Liebaers I, Bonduelle M, Van Assche E, Devroey P and Van Steirteghem A (1995) Sex chromosome abnormalities after intracytoplasmic sperm injection Lancet 346 1095
-
(1995)
Lancet
, vol.346
, pp. 1095
-
-
Liebaers, I.1
Bonduelle, M.2
Van Assche, E.3
Devroey, P.4
Van Steirteghem, A.5
-
48
-
-
0032992824
-
Estimates of sperm sex chromosome disomy and diploidy rates in a 47,XXY/46,XY mosaic Klinefelter patient
-
Lim AS, Fong Y and Yu SL (1999) Estimates of sperm sex chromosome disomy and diploidy rates in a 47,XXY/46,XY mosaic Klinefelter patient Human Genetics 104 405-409
-
(1999)
Human Genetics
, vol.104
, pp. 405-409
-
-
Lim, A.S.1
Fong, Y.2
Yu, S.L.3
-
49
-
-
0031761587
-
Abnormalities for chromosomes 13 and 21 detected in spermatozoa from infertile men
-
McInnes B, Rademaker A, Greene CA, Ko E, Barclay L and Martin R (1998) Abnormalities for chromosomes 13 and 21 detected in spermatozoa from infertile men Human Reproduction 13 2787-2790
-
(1998)
Human Reproduction
, vol.13
, pp. 2787-2790
-
-
McInnes, B.1
Rademaker, A.2
Greene, C.A.3
Ko, E.4
Barclay, L.5
Martin, R.6
-
50
-
-
0021344378
-
Analysis of human sperm chromosome complements from a male heterozygous for a reciprocal translocation t(11;22)(q23;q11)
-
Martin RH (1984) Analysis of human sperm chromosome complements from a male heterozygous for a reciprocal translocation t(11;22)(q23;q11) Clinical Genetics 25 357-361
-
(1984)
Clinical Genetics
, vol.25
, pp. 357-361
-
-
Martin, R.H.1
-
51
-
-
0024230620
-
Cytogenetic analysis of sperm from a male heterozygous for a 13;14 Robertsonian translocation
-
Martin RH (1988) Cytogenetic analysis of sperm from a male heterozygous for a 13;14 Robertsonian translocation Human Genetics 80 357-361
-
(1988)
Human Genetics
, vol.80
, pp. 357-361
-
-
Martin, R.H.1
-
52
-
-
0343492241
-
Sperm cell - Genetic aspects
-
Eds JG Grudzinskas et al. Cambridge University Press, Cambridge
-
Martin RH (1995) Sperm cell - genetic aspects. In Cambridge Reviews in Human Reproduction pp 104-121 Eds JG Grudzinskas et al. Cambridge University Press, Cambridge
-
(1995)
Cambridge Reviews in Human Reproduction
, pp. 104-121
-
-
Martin, R.H.1
-
53
-
-
0029886954
-
The risk of chromosomal abnormalities following ICSI
-
Martin RH (1996) The risk of chromosomal abnormalities following ICSI Human Reproduction 11 924-925
-
(1996)
Human Reproduction
, vol.11
, pp. 924-925
-
-
Martin, R.H.1
-
54
-
-
0023904370
-
The relationship between sperm chromosomal abnormalities and sperm morphology in humans
-
Martin RH and Rademaker A (1988) The relationship between sperm chromosomal abnormalities and sperm morphology in humans Mutation Research 207 159-164
-
(1988)
Mutation Research
, vol.207
, pp. 159-164
-
-
Martin, R.H.1
Rademaker, A.2
-
55
-
-
0028855742
-
Sperm chromosome complements in a man heterozygous for a reciprocal translocation 46,XY,t(9;13)(q21.1;q21.2) and a review of the literature
-
Martin RH and Spriggs EL (1995) Sperm chromosome complements in a man heterozygous for a reciprocal translocation 46,XY,t(9;13)(q21.1;q21.2) and a review of the literature Clinical Genetics 47 42-46
-
(1995)
Clinical Genetics
, vol.47
, pp. 42-46
-
-
Martin, R.H.1
Spriggs, E.L.2
-
56
-
-
0033125279
-
Analysis of aneuploidy for chromosomes 13, 21, X, and Y by multicolour fluoresence in situ hybridization (FISH) in a 47,XYY male
-
Martin RH, McInnes B and Rademaker AW (1999) Analysis of aneuploidy for chromosomes 13, 21, X, and Y by multicolour fluoresence in situ hybridization (FISH) in a 47,XYY male Zygote 7 131-134
-
(1999)
Zygote
, vol.7
, pp. 131-134
-
-
Martin, R.H.1
McInnes, B.2
Rademaker, A.W.3
-
57
-
-
0034100519
-
Chromosome analysis of spermatozoa extracted from testes of men with non-obstructive azoospermia
-
Martin R, Greene C, Rademaker A, Barclay L, Ko E and Chernos J (2000) Chromosome analysis of spermatozoa extracted from testes of men with non-obstructive azoospermia Human Reproduction 15 1121-1124
-
(2000)
Human Reproduction
, vol.15
, pp. 1121-1124
-
-
Martin, R.1
Greene, C.2
Rademaker, A.3
Barclay, L.4
Ko, E.5
Chernos, J.6
-
58
-
-
0030807764
-
Sex chromosome aneuploidy in sperm-derived pronuclei, motile sperm and unselected sperm, scored by three-color FISH
-
Martinez-Pasarell O, Vidal F, Colls P, Nogues C, Egozcue J and Templado C (1997) Sex chromosome aneuploidy in sperm-derived pronuclei, motile sperm and unselected sperm, scored by three-color FISH Cytogenetics and Cell Genetics 78 27-30
-
(1997)
Cytogenetics and Cell Genetics
, vol.78
, pp. 27-30
-
-
Martinez-Pasarell, O.1
Vidal, F.2
Colls, P.3
Nogues, C.4
Egozcue, J.5
Templado, C.6
-
59
-
-
0031947450
-
Detection of structural abnormalities in spermatozoa of a translocation carrier t(3;11)(q27.3;q24.3) by triple FISH
-
Martini E, von Bergh A, Coonen E, de Die-Smulders C, Hopman A, Ramaekers F and Geraedts J (1998) Detection of structural abnormalities in spermatozoa of a translocation carrier t(3;11)(q27.3;q24.3) by triple FISH Human Genetics 102 157-165
-
(1998)
Human Genetics
, vol.102
, pp. 157-165
-
-
Martini, E.1
Von Bergh, A.2
Coonen, E.3
De Die-Smulders, C.4
Hopman, A.5
Ramaekers, F.6
Geraedts, J.7
-
60
-
-
0030178251
-
Analysis of the sex chromosomal equipment in spermatozoa of a 47,XYY male using two-colour fluorescence in situ hybridization
-
Mercier S, Morel F, Roux C, Clavequin MC and Bresson JL (1996) Analysis of the sex chromosomal equipment in spermatozoa of a 47,XYY male using two-colour fluorescence in situ hybridization Molecular Human Reproduction 2 485-488
-
(1996)
Molecular Human Reproduction
, vol.2
, pp. 485-488
-
-
Mercier, S.1
Morel, F.2
Roux, C.3
Clavequin, M.C.4
Bresson, J.L.5
-
61
-
-
0031899913
-
Molecular analysis of the chromosomal equipment in spermatozoa of a 46, XY, t(7;B)(q11.21;cen) carrier by using fluorescence in situ hybridization
-
Mercier S, Morel F, Fellman F, Roux C and Bresson J (1998) Molecular analysis of the chromosomal equipment in spermatozoa of a 46, XY, t(7;B)(q11.21;cen) carrier by using fluorescence in situ hybridization Human Genetics 102 446-451
-
(1998)
Human Genetics
, vol.102
, pp. 446-451
-
-
Mercier, S.1
Morel, F.2
Fellman, F.3
Roux, C.4
Bresson, J.5
-
62
-
-
0030842308
-
Intracytoplasmic sperm injection pregnancy with fetal trisomy 9p resulting from a balanced paternal translocation
-
Meschede D, Louwen F, Eiben B and Horst J (1997) Intracytoplasmic sperm injection pregnancy with fetal trisomy 9p resulting from a balanced paternal translocation Human Reproduction 12 1913-1914
-
(1997)
Human Reproduction
, vol.12
, pp. 1913-1914
-
-
Meschede, D.1
Louwen, F.2
Eiben, B.3
Horst, J.4
-
63
-
-
0028269490
-
Numerical chromosome abnormalities in spermatozoa of fertile and infertile men detected by fluorescence in situ hybridization
-
Miharu N, Best RG and Young SR (1994) Numerical chromosome abnormalities in spermatozoa of fertile and infertile men detected by fluorescence in situ hybridization Human Generics 93 502-506
-
(1994)
Human Generics
, vol.93
, pp. 502-506
-
-
Miharu, N.1
Best, R.G.2
Young, S.R.3
-
64
-
-
0029087947
-
Chromosomal analysis of sperm from men with idiopathic infertility using sperm karyotyping and fluorescence in situ hybridization
-
Moosani N, Pattinson H, Carter M, Cox D, Rademaker A and Martin R (1995) Chromosomal analysis of sperm from men with idiopathic infertility using sperm karyotyping and fluorescence in situ hybridization Fertility and Sterility 64 811-817
-
(1995)
Fertility and Sterility
, vol.64
, pp. 811-817
-
-
Moosani, N.1
Pattinson, H.2
Carter, M.3
Cox, D.4
Rademaker, A.5
Martin, R.6
-
65
-
-
0032891286
-
A 47,XXY fetus resulting from ICSI in a man with an elevated frequency of 24,XY spermatozoa
-
Moosani N, Chernos J, Lowry RB, Martin RH and Rademaker A (1999) A 47,XXY fetus resulting from ICSI in a man with an elevated frequency of 24,XY spermatozoa Human Reproduction 14 1137-1138
-
(1999)
Human Reproduction
, vol.14
, pp. 1137-1138
-
-
Moosani, N.1
Chernos, J.2
Lowry, R.B.3
Martin, R.H.4
Rademaker, A.5
-
66
-
-
0034049964
-
Segregation of sex chromosomes in spermatozoa of 46,XY/47,XXY men by multicolour fluorescence in situ hybridization
-
Morel F, Roux C and Bresson JL (2000) Segregation of sex chromosomes in spermatozoa of 46,XY/47,XXY men by multicolour fluorescence in situ hybridization Molecular Human Reproduction 6 566-570
-
(2000)
Molecular Human Reproduction
, vol.6
, pp. 566-570
-
-
Morel, F.1
Roux, C.2
Bresson, J.L.3
-
68
-
-
0034055237
-
Chromosome analysis of human spermatozoa from an oligoasthenozoospermic carrier for a 13;14 Robertsonian translocation by their injection into mouse oocytes
-
Ogawa S, Araki S, Araki Y, Ohno M and Sato I (2000) Chromosome analysis of human spermatozoa from an oligoasthenozoospermic carrier for a 13;14 Robertsonian translocation by their injection into mouse oocytes Human Reproduction 15 1136-1139
-
(2000)
Human Reproduction
, vol.15
, pp. 1136-1139
-
-
Ogawa, S.1
Araki, S.2
Araki, Y.3
Ohno, M.4
Sato, I.5
-
69
-
-
0032905397
-
Detection of aneuploidy for chromosomes 4, 6, 7, 8, 9, 10, 11, 12, 13, 17, 18, 21, X and Y by fluorescence in situ hybridization in spermatozoa from nine patients with oligoasthenoteratozoospermia undergoing intracytoplasmic sperm injection
-
* Pang M, Hoegerman S, Cuticchia A, Moon S, Doncel G, Acosta A and Kearns W (1999) Detection of aneuploidy for chromosomes 4, 6, 7, 8, 9, 10, 11, 12, 13, 17, 18, 21, X and Y by fluorescence in situ hybridization in spermatozoa from nine patients with oligoasthenoteratozoospermia undergoing intracytoplasmic sperm injection Human Reproduction 14 1266-1273
-
(1999)
Human Reproduction
, vol.14
, pp. 1266-1273
-
-
Pang, M.1
Hoegerman, S.2
Cuticchia, A.3
Moon, S.4
Doncel, G.5
Acosta, A.6
Kearns, W.7
-
70
-
-
0023351609
-
Chromosome analysis of spermatozoa from a male heterozygous for a 13;14 robertsonian translocation
-
Pellestor F, Sele B and Jalbert H (1987) Chromosome analysis of spermatozoa from a male heterozygous for a 13;14 Robertsonian translocation Human Genetics 76 116-120
-
(1987)
Human Genetics
, vol.76
, pp. 116-120
-
-
Pellestor, F.1
Sele, B.2
Jalbert, H.3
-
71
-
-
0031471552
-
Cytogenetic analysis of meiotic segregation in sperm from two males heterozygous for reciprocal translocations using PRINS and humster techniques
-
Pellestor F, Girardet A, Coignet L, Andreo B, Lefort G and Charlieu JP (1997) Cytogenetic analysis of meiotic segregation in sperm from two males heterozygous for reciprocal translocations using PRINS and humster techniques Cytogenetics and Cell Genetics 78 202-208
-
(1997)
Cytogenetics and Cell Genetics
, vol.78
, pp. 202-208
-
-
Pellestor, F.1
Girardet, A.2
Coignet, L.3
Andreo, B.4
Lefort, G.5
Charlieu, J.P.6
-
72
-
-
0033199457
-
Aneuploidy frequencies in semen fractions from ten oligoasthenoteratozoospermic patients donating sperm for intracytoplasmic sperm injection
-
Pfeffer J, Pang M, Hoegerman S, Osgood C, Stacey M, Mayer J, Oehninger S and Kearns W (1999) Aneuploidy frequencies in semen fractions from ten oligoasthenoteratozoospermic patients donating sperm for intracytoplasmic sperm injection Fertility and Sterility 72 472-478
-
(1999)
Fertility and Sterility
, vol.72
, pp. 472-478
-
-
Pfeffer, J.1
Pang, M.2
Hoegerman, S.3
Osgood, C.4
Stacey, M.5
Mayer, J.6
Oehninger, S.7
Kearns, W.8
-
73
-
-
0031872238
-
A birth in non-mosaic Klinefelter's syndrome after testicular fine needle aspiration, intracytoplasmic sperm injection and preimplantation genetic diagnosis
-
Reubinoff BE, Abeliovich D, Werner M, Schenker JG, Safran A and Lewin A (1998) A birth in non-mosaic Klinefelter's syndrome after testicular fine needle aspiration, intracytoplasmic sperm injection and preimplantation genetic diagnosis Human Reproduction 13 1887-1892
-
(1998)
Human Reproduction
, vol.13
, pp. 1887-1892
-
-
Reubinoff, B.E.1
Abeliovich, D.2
Werner, M.3
Schenker, J.G.4
Safran, A.5
Lewin, A.6
-
74
-
-
0032861094
-
Relationship between clinical phenotype, semen parameters and aneuploidy frequency in sperm nuclei of 50 infertile males
-
Rives N, Saint Clair A, Mazurier S, Sibert L, Simeon N, Joly G and Mace B (1999) Relationship between clinical phenotype, semen parameters and aneuploidy frequency in sperm nuclei of 50 infertile males Human Genetics 105 266-272
-
(1999)
Human Genetics
, vol.105
, pp. 266-272
-
-
Rives, N.1
Saint Clair, A.2
Mazurier, S.3
Sibert, L.4
Simeon, N.5
Joly, G.6
Mace, B.7
-
75
-
-
0033951072
-
Assessment of sex chromosome aneuploidy in sperm nuclei from 47,XXY and 46,XY/47,XXY males: Comparison with fertile and infertile males with normal karyotype
-
Rives N, Joly G, Machy A, Simeon N, Leclerc P and Mace B (2000) Assessment of sex chromosome aneuploidy in sperm nuclei from 47,XXY and 46,XY/47,XXY males: comparison with fertile and infertile males with normal karyotype Molecular Human Reproduction 6 107-112
-
(2000)
Molecular Human Reproduction
, vol.6
, pp. 107-112
-
-
Rives, N.1
Joly, G.2
Machy, A.3
Simeon, N.4
Leclerc, P.5
Mace, B.6
-
76
-
-
0032976733
-
Birth of a healthy neonate following the intracytoplasmic injection of testicular spermatozoa from a patient with Klinefelter's syndrome
-
Ron-el R, Friedler S, Strassburger D, Komarovsky D, Schachter M and Raziel A (1999) Birth of a healthy neonate following the intracytoplasmic injection of testicular spermatozoa from a patient with Klinefelter's syndrome Human Reproduction 14 368-370
-
(1999)
Human Reproduction
, vol.14
, pp. 368-370
-
-
Ron-el, R.1
Friedler, S.2
Strassburger, D.3
Komarovsky, D.4
Schachter, M.5
Raziel, A.6
-
77
-
-
0033800258
-
Birth of healthy male twins after intracytoplasmic sperm injection of frozen-thawed testicular spermatozoa from a patient with nonmosaic klinefelter syndrome
-
Ron-El R, Raziel A, Strassburger D, Schachter M, Bern O and Friedler S (2000a) Birth of healthy male twins after intracytoplasmic sperm injection of frozen-thawed testicular spermatozoa from a patient with nonmosaic Klinefelter syndrome Fertility and Sterility 74 832-833
-
(2000)
Fertility and Sterility
, vol.74
, pp. 832-833
-
-
Ron-El, R.1
Raziel, A.2
Strassburger, D.3
Schachter, M.4
Bern, O.5
Friedler, S.6
-
78
-
-
0033891355
-
A 47,XXY fetus conceived after icsi of spermatozoa from a patient with non-mosaic Klinefelter's syndrome: Case report
-
Ron-El R, Strassburger D, Gelman-Kohan S, Friedler S, Raziel A and Appelman Z (2000b) A 47,XXY fetus conceived after ICSI of spermatozoa from a patient with non-mosaic Klinefelter's syndrome: case report Human Reproduction 15 1804-1806
-
(2000)
Human Reproduction
, vol.15
, pp. 1804-1806
-
-
Ron-El, R.1
Strassburger, D.2
Gelman-Kohan, S.3
Friedler, S.4
Raziel, A.5
Appelman, Z.6
-
79
-
-
0028841197
-
Sperm nuclei analysis of a Robertsonian t(14q;21q) carrier, by FISH, using three plasmids and two YAC probes
-
Rousseaux S, Chevret E, Monteil M, Cozzi J, Pelletier R, Delafontaine D and Sele B (1995a) Sperm nuclei analysis of a Robertsonian t(14q;21q) carrier, by FISH, using three plasmids and two YAC probes Human Genetics 96 655-660
-
(1995)
Human Genetics
, vol.96
, pp. 655-660
-
-
Rousseaux, S.1
Chevret, E.2
Monteil, M.3
Cozzi, J.4
Pelletier, R.5
Delafontaine, D.6
Sele, B.7
-
80
-
-
0028869099
-
Meiatic segregation in males heterogote for reciprocal translocations: Analysis of sperm nuclei by two and three colour fluorescence in situ hybridization
-
Rousseaux S, Chevret E, Monteil M, Cozzi J, Pelletier R, Devillard F, Lespinasse J and Sele B (1995b) Meiatic segregation in males heterogote for reciprocal translocations: analysis of sperm nuclei by two and three colour fluorescence in situ hybridization Cytogenetics and Cell Genetics? 71 240-246
-
(1995)
Cytogenetics and Cell Genetics?
, vol.71
, pp. 240-246
-
-
Rousseaux, S.1
Chevret, E.2
Monteil, M.3
Cozzi, J.4
Pelletier, R.5
Devillard, F.6
Lespinasse, J.7
Sele, B.8
-
81
-
-
7344224406
-
Elucidating the mechanisms of paternal non-disjunction of chromosome 21 in humans
-
Savage AR, Petersen MB, Pettay D, Taft L, Allran K, Freeman SB, Karadima G, Avramopoulos D, Torfs C, Mikkelsen M, Hassold TJ and Sherman SL (1998) Elucidating the mechanisms of paternal non-disjunction of chromosome 21 in humans Human Molecular Genetics 7 1221-1227
-
(1998)
Human Molecular Genetics
, vol.7
, pp. 1221-1227
-
-
Savage, A.R.1
Petersen, M.B.2
Pettay, D.3
Taft, L.4
Allran, K.5
Freeman, S.B.6
Karadima, G.7
Avramopoulos, D.8
Torfs, C.9
Mikkelsen, M.10
Hassold, T.J.11
Sherman, S.L.12
-
82
-
-
0034528943
-
Aneuploidy in human sperm: A review of the frequency and distribution of aneuploidy, effects of donor age and lifestyle factors
-
* Shi Q and Martin RH (2000a) Aneuploidy in human sperm: a review of the frequency and distribution of aneuploidy, effects of donor age and lifestyle factors Cytogenetics and Cell Genetics 90 219-226
-
(2000)
Cytogenetics and Cell Genetics
, vol.90
, pp. 219-226
-
-
Shi, Q.1
Martin, R.H.2
-
83
-
-
0034601120
-
Multicolor fluorescence in situ hybridization analysis of meiotic chromosome segregation in a 47,XYY male and a review of the literature
-
* Shi Q and Martin RH (2000b) Multicolor fluorescence in situ hybridization analysis of meiotic chromosome segregation in a 47,XYY male and a review of the literature American Journal of Medical Genetics 93 40-46
-
(2000)
American Journal of Medical Genetics
, vol.93
, pp. 40-46
-
-
Shi, Q.1
Martin, R.H.2
-
84
-
-
0035865957
-
Single sperm typing demonstrates that reduced recombination is associated with the production of aneuploid 24,XY human sperm
-
Shi Q, Spriggs E, Field LL, Ko E, Barclay L and Martin RH (2001) Single sperm typing demonstrates that reduced recombination is associated with the production of aneuploid 24,XY human sperm American Journal of Medical Genetics 99 34-38
-
(2001)
American Journal of Medical Genetics
, vol.99
, pp. 34-38
-
-
Shi, Q.1
Spriggs, E.2
Field, L.L.3
Ko, E.4
Barclay, L.5
Martin, R.H.6
-
85
-
-
0028290235
-
Analysis of segregation in a human male reciprocal translocation carrier, t(1;11) (p36.3;q13.1), by two-colour fluorescence in situ hybridization
-
Spriggs EL and Martin RH (1994) Analysis of segregation in a human male reciprocal translocation carrier, t(1;11) (p36.3;q13.1), by two-colour fluorescence in situ hybridization Molecular Reproduction and Developments 38 247-250
-
(1994)
Molecular Reproduction and Developments
, vol.38
, pp. 247-250
-
-
Spriggs, E.L.1
Martin, R.H.2
-
86
-
-
0014685973
-
Transmission of 47, XYY karyotype?
-
Sundequist U and Hellstrom E (1969) Transmission of 47, XYY karyotype? Lancet 2 1367
-
(1969)
Lancet
, vol.2
, pp. 1367
-
-
Sundequist, U.1
Hellstrom, E.2
-
87
-
-
0021238541
-
Meiotic studies and synaptonemal complex analysis in two infertile males with a 13/14 balanced translocation
-
Templado C, Vidal F, Navarro J, Marina S and Egozcue J (1984) Meiotic studies and synaptonemal complex analysis in two infertile males with a 13/14 balanced translocation Human Genetics 67 162-165
-
(1984)
Human Genetics
, vol.67
, pp. 162-165
-
-
Templado, C.1
Vidal, F.2
Navarro, J.3
Marina, S.4
Egozcue, J.5
-
88
-
-
0005516387
-
Clinical cytogenetics: General principles and autosomal abnormalities
-
Eds MW Thompson et al. WB Saunders, Toronto
-
Thompson MW, McInnes RR and Willard HF (1986) Clinical cytogenetics: general principles and autosomal abnormalities. In Genetics in Medicine 5th Edn pp 201-229 Eds MW Thompson et al. WB Saunders, Toronto
-
(1986)
Genetics in Medicine 5th Edn
, pp. 201-229
-
-
Thompson, M.W.1
McInnes, R.R.2
Willard, H.F.3
-
89
-
-
0034110458
-
Analysis of chromosomal abnormalities in human spermatozoa using multi-colour fluorescence in situ hybridization
-
Ushijima C, Kumasako Y, Kihaile PE, Hirotsuru K and Utsunomiya T (2000) Analysis of chromosomal abnormalities in human spermatozoa using multi-colour fluorescence in situ hybridization Human Reproduction 15 1107-1111
-
(2000)
Human Reproduction
, vol.15
, pp. 1107-1111
-
-
Ushijima, C.1
Kumasako, Y.2
Kihaile, P.E.3
Hirotsuru, K.4
Utsunomiya, T.5
-
90
-
-
0032980063
-
Preimplantation genetic diagnosis and sperm analysis by fluorescence in situ hybridization for the most common reciprocal translocation t(11;22)
-
Van Assche E, Staessen C, Vegetti W, Bonduelle M, Vandervorst M, Van Steirteghem A and Liebaers I (1999) Preimplantation genetic diagnosis and sperm analysis by fluorescence in situ hybridization for the most common reciprocal translocation t(11;22) Molecular Human Reproduction 5 682-690
-
(1999)
Molecular Human Reproduction
, vol.5
, pp. 682-690
-
-
Van Assche, E.1
Staessen, C.2
Vegetti, W.3
Bonduelle, M.4
Vandervorst, M.5
Van Steirteghem, A.6
Liebaers, I.7
-
91
-
-
0030773488
-
Meiotic segregation, recombination, and gamete aneuploidy assessed in a t(1;10)(p22.1;q22.3) reciprocal translocation carrier by three- and four-probe multicolor FISH in sperm
-
Van Hummelen P, Manchester D, Lowe X and Wyrobek A (1997) Meiotic segregation, recombination, and gamete aneuploidy assessed in a t(1;10)(p22.1;q22.3) reciprocal translocation carrier by three- and four-probe multicolor FISH in sperm American Journal of Human Genetics 61 651-659
-
(1997)
American Journal of Human Genetics
, vol.61
, pp. 651-659
-
-
Van Hummelen, P.1
Manchester, D.2
Lowe, X.3
Wyrobek, A.4
-
92
-
-
0030918389
-
Determination of the parent of origin in nine cases of prenatally detected chromosome aberrations found after intracytoplasmic sperm injection
-
* Van Opstal D, Los FJ, Ramlakhan S, Van Hemel JO, Van Den Ouweland AM, Brandenburg H, Pieters MH, Verhoeff A, Vermeer MC, Dhont M and In't Veld PA (1997) Determination of the parent of origin in nine cases of prenatally detected chromosome aberrations found after intracytoplasmic sperm injection Human Reproduction 12 682-686
-
(1997)
Human Reproduction
, vol.12
, pp. 682-686
-
-
Van Opstal, D.1
Los, F.J.2
Ramlakhan, S.3
Van Hemel, J.O.4
Van Den Ouweland, A.M.5
Brandenburg, H.6
Pieters, M.H.7
Verhoeff, A.8
Vermeer, M.C.9
Dhont, M.10
In't Veld, P.A.11
-
93
-
-
0033958837
-
Correlation between semen parameters and sperm aneuploidy rates investigated by fluorescence in situ hybridization in infertile men
-
Vegetti W, Van Assche E, Frias A, Verheyen G, Bianchi MM, Bonduelle M, Liebaers I and Van Steirteghem A (2000) Correlation between semen parameters and sperm aneuploidy rates investigated by fluorescence in situ hybridization in infertile men Human Reproduction 15 351-365
-
(2000)
Human Reproduction
, vol.15
, pp. 351-365
-
-
Vegetti, W.1
Van Assche, E.2
Frias, A.3
Verheyen, G.4
Bianchi, M.M.5
Bonduelle, M.6
Liebaers, I.7
Van Steirteghem, A.8
-
94
-
-
0020062543
-
Meiotic and synaptonemal complex studies in a 14/21 translocation carrier
-
Vidal F, Templado C, Navarro J, Marina S and Egozcue J (1982) Meiotic and synaptonemal complex studies in a 14/21 translocation carrier International Journal of Andrology 5 21-26
-
(1982)
International Journal of Andrology
, vol.5
, pp. 21-26
-
-
Vidal, F.1
Templado, C.2
Navarro, J.3
Marina, S.4
Egozcue, J.5
-
96
-
-
0034066189
-
Congenital malformations after intracytoplasmic injection of spermatids
-
Zech H, Vanderzwalmen P, Prapas Y, Lejeune B, Duba E and Schoysman R (2000) Congenital malformations after intracytoplasmic injection of spermatids Human Reproduction 15 969-971
-
(2000)
Human Reproduction
, vol.15
, pp. 969-971
-
-
Zech, H.1
Vanderzwalmen, P.2
Prapas, Y.3
Lejeune, B.4
Duba, E.5
Schoysman, R.6
-
97
-
-
0034078804
-
Detection of chromosomal abnormalities by fluorescent in-situ hybridization in immotile viable spermatozoa determined by hypo-osmotic sperm swelling test
-
Zeyneloglu HB, Baltaci V, Ege S, Haberal A and Batioglu S (2000) Detection of chromosomal abnormalities by fluorescent in-situ hybridization in immotile viable spermatozoa determined by hypo-osmotic sperm swelling test Human Reproduction 15 853-856
-
(2000)
Human Reproduction
, vol.15
, pp. 853-856
-
-
Zeyneloglu, H.B.1
Baltaci, V.2
Ege, S.3
Haberal, A.4
Batioglu, S.5
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