-
1
-
-
0021917574
-
Forty-four probands with additional "marker" chromosome
-
Buckton KE, Spowart G, Newton MS, Evans HJ: Forty-four probands with additional "marker" chromosome. Hum Genet, 1985; 69: 353-70
-
(1985)
Hum Genet
, vol.69
, pp. 353-370
-
-
Buckton, K.E.1
Spowart, G.2
Newton, M.S.3
Evans, H.J.4
-
2
-
-
0028027588
-
Swedish survey on extra structurally abnormal chromosomes in 39,105 consecutive prenatal diagnoses: Prevalence and characterization by fluorescence in situ hybridization
-
Blennow E, Bui T-H, Kristoffersson U et al: Swedish survey on extra structurally abnormal chromosomes in 39,105 consecutive prenatal diagnoses: prevalence and characterization by fluorescence in situ hybridization. Prenatal Diag, 1994; 14: 1019-28
-
(1994)
Prenatal Diag
, vol.14
, pp. 1019-1028
-
-
Blennow, E.1
Bui, T.-H.2
Kristoffersson, U.3
-
3
-
-
0026602327
-
Two extra inv dup(del 15) chromosomes and male infertility: Second case
-
Manenti E: Two extra inv dup(del 15) chromosomes and male infertility: second case. Am J Med Genet, 1992; 42: 402-3
-
(1992)
Am J Med Genet
, vol.42
, pp. 402-403
-
-
Manenti, E.1
-
4
-
-
0030455185
-
Milotic chromosomal anomalies among 1210 infertile men
-
Pandiyan N, Jequier MA: Milotic chromosomal anomalies among 1210 infertile men. Human Reprod, 1996; 11: 2604-8
-
(1996)
Human Reprod
, vol.11
, pp. 2604-2608
-
-
Pandiyan, N.1
Jequier, M.A.2
-
5
-
-
0031469084
-
Molecular cytogenetic diagnosis in sperm
-
Mennicke K, Diercks P, Schlieker H_et al: Molecular cytogenetic diagnosis in sperm. Int J Andr, 1997; 20(Suppl.3): 11-19
-
(1997)
Int J Andr
, vol.20
, Issue.SUPPL. 3
, pp. 11-19
-
-
Mennicke, K.1
Diercks, P.2
Schlieker, H.3
-
7
-
-
13144251121
-
Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: The Dutch experience
-
Tuerlings JH, de France HF, Hamers A et al: Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience. Eur J Hum Genet, 1998;6: 194-200
-
(1998)
Eur J Hum Genet
, vol.6
, pp. 194-200
-
-
Tuerlings, J.H.1
De France, H.F.2
Hamers, A.3
-
8
-
-
0035147333
-
Idiopatic infertility of married couples in the light of cytogenetic analysis and sperm penetration assay
-
Wiland E, Wojda A, Kamieniczna M et al: Idiopatic infertility of married couples in the light of cytogenetic analysis and sperm penetration assay. Folia Histochem Cytobiol, 2001; 39:35-41
-
(2001)
Folia Histochem Cytobiol
, vol.39
, pp. 35-41
-
-
Wiland, E.1
Wojda, A.2
Kamieniczna, M.3
-
9
-
-
0028947788
-
Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization
-
Blennow E, Nielsen KB, Telenius H et al: Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization. Am J Med Genet, 1995; 55: 85-94
-
(1995)
Am J Med Genet
, vol.55
, pp. 85-94
-
-
Blennow, E.1
Nielsen, K.B.2
Telenius, H.3
-
10
-
-
0025007098
-
The isochromosome 18p syndrome: Confirmation of cytogenetic diagnosis in nine cases by in situ hybridization
-
Callen DF, Freemantle CJ, Ringenbergs ML et al: The isochromosome 18p syndrome: Confirmation of cytogenetic diagnosis in nine cases by in situ hybridization. Am J Hum Genet, 1990; 47: 493-98
-
(1990)
Am J Hum Genet
, vol.47
, pp. 493-498
-
-
Callen, D.F.1
Freemantle, C.J.2
Ringenbergs, M.L.3
-
11
-
-
0026700258
-
Typical and partial cat eye syndrome: Identification of marker chromosome by FISH
-
Liehr T, Pfeiffer RA, Trautmann U: Typical and partial cat eye syndrome: Identification of marker chromosome by FISH, Clin Genet, 1992; 42: 91-96
-
(1992)
Clin Genet
, vol.42
, pp. 91-96
-
-
Liehr, T.1
Pfeiffer, R.A.2
Trautmann, U.3
-
12
-
-
0027318279
-
Molecular cytogenetic study of patients with Pallister-Killian syndrome
-
Larramendy M, Heiskanen M, Wessmann M et al: Molecular cytogenetic study of patients with Pallister-Killian syndrome. Hum Genet, 1993; 91: 121-27
-
(1993)
Hum Genet
, vol.91
, pp. 121-127
-
-
Larramendy, M.1
Heiskanen, M.2
Wessmann, M.3
-
13
-
-
0027370553
-
Prenatal diagnosis and clinical findings in a case of hexasomy 12p
-
Van den Veyver IB, Macha ME, McCaskill C et al: Prenatal diagnosis and clinical findings in a case of hexasomy 12p. Am J Med Genet, 1993; 47: 1171-74
-
(1993)
Am J Med Genet
, vol.47
, pp. 1171-1174
-
-
Van Den Veyver, I.B.1
Macha, M.E.2
McCaskill, C.3
-
14
-
-
0035869201
-
Detailed characterization of 12 supernumerary ring chromosomes using micro-FlSH and search for uniparental disomy
-
Anderlid BM, Sahlen S, Schoumans J et al: Detailed characterization of 12 supernumerary ring chromosomes using micro-FlSH and search for uniparental disomy. Am J Med Genet, 2001; 99: 223-33
-
(2001)
Am J Med Genet
, vol.99
, pp. 223-233
-
-
Anderlid, B.M.1
Sahlen, S.2
Schoumans, J.3
-
15
-
-
0036796014
-
Supernumerary marker chromosomes (SMC) and uniparen-tal disomy (UPD): Coincidence or consequence?
-
Kotzot D: Supernumerary marker chromosomes (SMC) and uniparen-tal disomy (UPD): coincidence or consequence? J Med Genet, 2002; 39: 775-7
-
(2002)
J Med Genet
, vol.39
, pp. 775-777
-
-
Kotzot, D.1
-
16
-
-
10744232485
-
Small supernumerary marker chromosomes (SMCs): Genotype-phenotype correlation and classification
-
Starke H, Nietzel A, Weise A et al: Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification. Hum Genet, 2003; 114: 51-67
-
(2003)
Hum Genet
, vol.114
, pp. 51-67
-
-
Starke, H.1
Nietzel, A.2
Weise, A.3
-
17
-
-
0345448878
-
Supernumerary small marker chromosome (SMC) and uniparental disomy 22 in a child with confined placental mosaicism of trisomy 22: Trisomy rescue due to marker chro-mosome formation
-
Bartels I, Schlueter G, Liehr T et al: Supernumerary small marker chromosome (SMC) and uniparental disomy 22 in a child with confined placental mosaicism of trisomy 22: trisomy rescue due to marker chro-mosome formation. Cytogenet Genome Res, 2003, 101: 103-5
-
(2003)
Cytogenet Genome Res
, vol.101
, pp. 103-105
-
-
Bartels, I.1
Schlueter, G.2
Liehr, T.3
-
18
-
-
0036665170
-
Supernumerary marker chromosomes derived from chromosome 15: Analysis of 32 new cases
-
Eggermann K, Mau UA, Bujdoso G et al: Supernumerary marker chromosomes derived from chromosome 15: analysis of 32 new cases. Clin Genet, 2002; 62: 89-93
-
(2002)
Clin Genet
, vol.62
, pp. 89-93
-
-
Eggermann, K.1
Mau, U.A.2
Bujdoso, G.3
-
19
-
-
15944375607
-
A supermumerary chromosome 20, identified by FISH, in a male with azoospermia - Cause or coincidence
-
Mc Nerlan SE, Morrison PJ, Mc Clure N, Nevin NC: A supermumerary chromosome 20, identified by FISH, in a male with azoospermia - cause or coincidence. Am J Med Genet, 2002; 9999: 1-3
-
(2002)
Am J Med Genet
, vol.9999
, pp. 1-3
-
-
Mc Nerlan, S.E.1
Morrison, P.J.2
Mc Clure, N.3
Nevin, N.C.4
-
20
-
-
0022543855
-
Infertility associated with two accessory bisatellited chromosomes
-
Martin-Lucas MA, Perez-Casollo A, Abrisqueta JA: Infertility associated with two accessory bisatellited chromosomes. Hum Genet, 1986; 73: 133-36
-
(1986)
Hum Genet
, vol.73
, pp. 133-136
-
-
Martin-Lucas, M.A.1
Perez-Casollo, A.2
Abrisqueta, J.A.3
-
21
-
-
0028241087
-
Supernumerary chromosomes and spermatogenesis in a human male carrier
-
Jaafar H, Gabriel-Robez O, Vignon F et al: Supernumerary chromosomes and spermatogenesis in a human male carrier. Hum Genet, 1994; 94: 74-76
-
(1994)
Hum Genet
, vol.94
, pp. 74-76
-
-
Jaafar, H.1
Gabriel-Robez, O.2
Vignon, F.3
-
22
-
-
0027164995
-
Infertility in carriers of two bisatellited marker chromosomes
-
Gentile M, Susca F, Resta et al: Infertility in carriers of two bisatellited marker chromosomes. Clin Genet, 1993; 44: 71-75
-
(1993)
Clin Genet
, vol.44
, pp. 71-75
-
-
Gentile, M.1
Susca, F.2
Resta3
-
24
-
-
0037545617
-
The frequency of antisperm antibodies in infertile couples - A Polish pilot study
-
Kamieniczna M, Domagala A, Kurpisz M: The frequency of antisperm antibodies in infertile couples - a Polish pilot study. Med Sci Monit, 2003, 9(4): CR194-201
-
(2003)
Med Sci Monit
, vol.9
, Issue.4
-
-
Kamieniczna, M.1
Domagala, A.2
Kurpisz, M.3
-
26
-
-
0027486737
-
Detection of aneuploid human sperm by fluorescence in situ hybridization: Evidence for donor difference in frequency of sperm disomic for chromosome 1 and Y
-
Robbins WA, Segraves R, Pinkel D, Wyrobek AJ: Detection of aneuploid human sperm by fluorescence in situ hybridization: evidence for donor difference in frequency of sperm disomic for chromosome 1 and Y. Am J Hum Genet, 1993; 52: 799-807
-
(1993)
Am J Hum Genet
, vol.52
, pp. 799-807
-
-
Robbins, W.A.1
Segraves, R.2
Pinkel, D.3
Wyrobek, A.J.4
-
27
-
-
0031879425
-
Assessment of autosome and gonosome disomy in human sperm nuclei by chromosome painting
-
Rives N, Mazurier S, Bellet D et al: Assessment of autosome and gonosome disomy in human sperm nuclei by chromosome painting. Hum Genet, 1998; 102: 616-23
-
(1998)
Hum Genet
, vol.102
, pp. 616-623
-
-
Rives, N.1
Mazurier, S.2
Bellet, D.3
-
28
-
-
0020955264
-
A detailed method for obtaining preparations of human sperm chromosomes
-
Martin RH: A detailed method for obtaining preparations of human sperm chromosomes. Cytogenet Cell Genet, 1983; 35: 252-56
-
(1983)
Cytogenet Cell Genet
, vol.35
, pp. 252-256
-
-
Martin, R.H.1
-
29
-
-
0036271462
-
Infertility status of male individuals with abnormal spermiogram evaluated by cytogenetic analysis and in vitro sperm penetration assay
-
Wiland E, Wojda A, Kamieniczna M et al: Infertility status of male individuals with abnormal spermiogram evaluated by cytogenetic analysis and in vitro sperm penetration assay. Med Sci Monit, 2002; 8: 394-400
-
(2002)
Med Sci Monit
, vol.8
, pp. 394-400
-
-
Wiland, E.1
Wojda, A.2
Kamieniczna, M.3
-
30
-
-
0030770720
-
Familial transmission of a small supernumerary marker chromosome 8 identified by FISH: An update
-
Rothenmund H, Chudley AE, Dawson AJ: Familial transmission of a small supernumerary marker chromosome 8 identified by FISH: an update. Am J Med Genet, 1997; 72: 339-42
-
(1997)
Am J Med Genet
, vol.72
, pp. 339-342
-
-
Rothenmund, H.1
Chudley, A.E.2
Dawson, A.J.3
-
31
-
-
0025911027
-
Chromosomal origin of small ring marker chromosomes in man: Characterization by molecular genetics
-
Callen DF, Eyre HJ, Ringenbergs ML et al: Chromosomal origin of small ring marker chromosomes in man: characterization by molecular genetics. Am J Med Genet, 1991; 48: 769-82
-
(1991)
Am J Med Genet
, vol.48
, pp. 769-782
-
-
Callen, D.F.1
Eyre, H.J.2
Ringenbergs, M.L.3
-
32
-
-
0027485183
-
Characterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH)
-
Blennow E, Anneren G, Bui T-H et al: Characterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH). Am J Hum Genet, 1993; 53: 433-42
-
(1993)
Am J Hum Genet
, vol.53
, pp. 433-442
-
-
Blennow, E.1
Anneren, G.2
Bui, T.-H.3
-
33
-
-
0028934283
-
An accessory marker derived from chromosome 20 and its co-existence with a mosaic trisomy 20 cell line
-
Batista DA, Escallon C, Blakemore KJ, Stetten G: An accessory marker derived from chromosome 20 and its co-existence with a mosaic trisomy 20 cell line. Prenatal Diag, 1995; 15:123-27
-
(1995)
Prenatal Diag
, vol.15
, pp. 123-127
-
-
Batista, D.A.1
Escallon, C.2
Blakemore, K.J.3
Stetten, G.4
-
34
-
-
0029962240
-
Supernumerary ring chromosome 20 characterized by fluorescence in situ hybridization
-
Van Langen IM, Otter MA, Aronson DC et al: Supernumerary ring chromosome 20 characterized by fluorescence in situ hybridization, Clin Genet, 1996; 49:49-53
-
(1996)
Clin Genet
, vol.49
, pp. 49-53
-
-
Van Langen, I.M.1
Otter, M.A.2
Aronson, D.C.3
-
35
-
-
0030951849
-
Identification of supernumerary der(20) chromosomes by FISH in three patients
-
Viersbach R, Engels H, Schwanitz G: Identification of supernumerary der(20) chromosomes by FISH in three patients. Am J Med Genet, 1997; 70:278-83
-
(1997)
Am J Med Genet
, vol.70
, pp. 278-283
-
-
Viersbach, R.1
Engels, H.2
Schwanitz, G.3
-
36
-
-
0032477780
-
FISH and molecular study of autosomal supernumerary marker chromosomes excluding those derived from chromosomes 15 and 22: I. Results of 26 new cases
-
Crolla JA, Long F, Rivera H, Dennis NR: FISH and molecular study of autosomal supernumerary marker chromosomes excluding those derived from chromosomes 15 and 22: I. Results of 26 new cases. Am J Med Genet, 1998; 75: 355-66
-
(1998)
Am J Med Genet
, vol.75
, pp. 355-366
-
-
Crolla, J.A.1
Long, F.2
Rivera, H.3
Dennis, N.R.4
-
37
-
-
0032787806
-
Maternal UPD 20 in a hyperactive child with severe growth retardation
-
Chudoba I, Franke Y, Senger G, et al: Maternal UPD 20 in a hyperactive child with severe growth retardation, Eur J Hum Genet, 1999; 7: 533-40
-
(1999)
Eur J Hum Genet
, vol.7
, pp. 533-540
-
-
Chudoba, I.1
Franke, Y.2
Senger, G.3
-
38
-
-
0034020593
-
Clinical findings in a patient mosaic for a supernumerary ring chromosome 20
-
Austin-Ward ED, Castillo S, Dragnic Y et al: Clinical findings in a patient mosaic for a supernumerary ring chromosome 20. Am J Med Genet, 2000; 91: 171-74
-
(2000)
Am J Med Genet
, vol.91
, pp. 171-174
-
-
Austin-Ward, E.D.1
Castillo, S.2
Dragnic, Y.3
-
39
-
-
0034011451
-
T Identification of supernumerary marker chromosomes derived from chromosomes 5, 6, 19, and 20 using FISH
-
Stankiewicz P, Bocian E, Jakubow-Durska K et al: T Identification of supernumerary marker chromosomes derived from chromosomes 5, 6, 19, and 20 using FISH. J Med Genet, 2000; 37: 114-20
-
(2000)
J Med Genet
, vol.37
, pp. 114-120
-
-
Stankiewicz, P.1
Bocian, E.2
Jakubow-Durska, K.3
-
40
-
-
0034925097
-
A non-sex chromosome marker in a patient with an atypical Ullrich-Turner phenotype and niosaicism of 46,X,mar/46,XX
-
Gray BA, Bent-Williams A, Wolff DJ, Zori RT: A non-sex chromosome marker in a patient with an atypical Ullrich-Turner phenotype and niosaicism of 46,X,mar/46,XX. Clin Genet, 2001; 60: 73-76
-
(2001)
Clin Genet
, vol.60
, pp. 73-76
-
-
Gray, B.A.1
Bent-Williams, A.2
Wolff, D.J.3
Zori, R.T.4
-
41
-
-
0022504711
-
The meiotic segregation of human sperm chromosomes in two men with accessory marker chromosomes
-
Martin RH, Hildebrand KA, Yamamoto J et al: The meiotic segregation of human sperm chromosomes in two men with accessory marker chromosomes. Am J Med Genet, 1986; 25: 381-88
-
(1986)
Am J Med Genet
, vol.25
, pp. 381-388
-
-
Martin, R.H.1
Hildebrand, K.A.2
Yamamoto, J.3
-
42
-
-
0034535486
-
Segregation of a supernumerary del (15) marker chromosome in sperm
-
Cotter PD, Ko E, Larabell SK et al: Segregation of a supernumerary del (15) marker chromosome in sperm. Clin Genet, 2000; 58: 488-92
-
(2000)
Clin Genet
, vol.58
, pp. 488-492
-
-
Cotter, P.D.1
Ko, E.2
Larabell, S.K.3
-
43
-
-
0023754181
-
Renew and hypothesis: Somatic mosaicism: Observations related to clinical genetics
-
Hall JG: Renew and hypothesis: somatic mosaicism: observations related to clinical genetics. Am J Hum Genet, 1988; 43: 355-63
-
(1988)
Am J Hum Genet
, vol.43
, pp. 355-363
-
-
Hall, J.G.1
-
44
-
-
0024419361
-
Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism
-
Thomas IT, Frias JL, Cantu ES et al: Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism. Am J Hum Genet, 1989; 45: 193-205
-
(1989)
Am J Hum Genet
, vol.45
, pp. 193-205
-
-
Thomas, I.T.1
Frias, J.L.2
Cantu, E.S.3
-
45
-
-
0027976191
-
Dynamic mosaicism involving an unstable supernumerary der(22) chromosome in cat eye syndrome
-
Urioste M, Visedo G, Sanchis A et al: Dynamic mosaicism involving an unstable supernumerary der(22) chromosome in cat eye syndrome, Am J Med Genet 1994; 49: 77-82
-
(1994)
Am J Med Genet
, vol.49
, pp. 77-82
-
-
Urioste, M.1
Visedo, G.2
Sanchis, A.3
-
46
-
-
0017140969
-
The use of zona-free animal ova as a test-system for the assessment of the fertilizing capacity of human spermatozoa
-
Yanagimachi R, Yanagimachi H, Rogers BJ: The use of zona-free animal ova as a test-system for the assessment of the fertilizing capacity of human spermatozoa. Biol Reprod, 1976; 15: 471-76
-
(1976)
Biol Reprod
, vol.15
, pp. 471-476
-
-
Yanagimachi, R.1
Yanagimachi, H.2
Rogers, B.J.3
-
47
-
-
0030911181
-
Marker chromosomes in fetal loss
-
Kumar C, Kleyman SM, Samonte RV, Venna RS: Marker chromosomes in fetal loss. Hum Reprod, 1997; 12: 1321-24
-
(1997)
Hum Reprod
, vol.12
, pp. 1321-1324
-
-
Kumar, C.1
Kleyman, S.M.2
Samonte, R.V.3
Venna, R.S.4
-
48
-
-
0037339958
-
Prenatal diagnosis of a karyotypically normal pregnancy in a mother with a supernumerary neocentric 13q21→13q22 chromosome and balancing reciprocal deletion
-
Knegh AC, Li S, Engelen JJ et al: Prenatal diagnosis of a karyotypically normal pregnancy in a mother with a supernumerary neocentric 13q21→13q22 chromosome and balancing reciprocal deletion. Prenat Diagn, 2002; 23: 215-20
-
(2002)
Prenat Diagn
, vol.23
, pp. 215-220
-
-
Knegh, A.C.1
Li, S.2
Engelen, J.J.3
-
49
-
-
0031694581
-
Spermatozoa with chromosomal abnormalities may result in a higher rate of recurrent abortion
-
Giorlandino C, Calugi G, Iaconianni L et al: Spermatozoa with chromosomal abnormalities may result in a higher rate of recurrent abortion. Fertil Steril, 1998; 70: 576-77
-
(1998)
Fertil Steril
, vol.70
, pp. 576-577
-
-
Giorlandino, C.1
Calugi, G.2
Iaconianni, L.3
-
50
-
-
0032911570
-
Implications of sperm chromosome abnormalities in recurrent miscarriage
-
Rubio C, Simon C, BlancoJ et al: Implications of sperm chromosome abnormalities in recurrent miscarriage. J Assist Reprod Genet, 1999; 16(5): 253-58
-
(1999)
J Assist Reprod Genet
, vol.16
, Issue.5
, pp. 253-258
-
-
Rubio, C.1
Simon, C.2
Blanco, J.3
-
51
-
-
0035213251
-
The origin of abnormalities in recurrent aneuploidy/polyploidy
-
Robinson WP, McFadden DE, Stephenson MD: The origin of abnormalities in recurrent aneuploidy/polyploidy. Am J Hum Genet, 2001; 69: 1245-54
-
(2001)
Am J Hum Genet
, vol.69
, pp. 1245-1254
-
-
Robinson, W.P.1
McFadden, D.E.2
Stephenson, M.D.3
|