-
4
-
-
0030769649
-
-
Abdous A, Pen-Ming L. Ming, Hosam T, Salem E, Reece A. The clinical importance of pericentric inversion of chromosome 9 in prenatal diagnosis. J Mat Fetal Investigation 1997;7:126-8.
-
Abdous A, Pen-Ming L. Ming, Hosam T, Salem E, Reece A. The clinical importance of pericentric inversion of chromosome 9 in prenatal diagnosis. J Mat Fetal Investigation 1997;7:126-8.
-
-
-
-
5
-
-
0031438120
-
Homozygosity for pericentric inversions of chromosome 9. Prenatal diagnosis of two cases
-
Cotter PD, Babu A, McCurdy LD, Caggana M, Willner JP, Desnick RJ. Homozygosity for pericentric inversions of chromosome 9. Prenatal diagnosis of two cases. Ann Genet 1997;40:222-6.
-
(1997)
Ann Genet
, vol.40
, pp. 222-226
-
-
Cotter, P.D.1
Babu, A.2
McCurdy, L.D.3
Caggana, M.4
Willner, J.P.5
Desnick, R.J.6
-
6
-
-
0347072532
-
Chromosomal aberrations in children with suspected genetic disorders
-
Mokhtar MM. Chromosomal aberrations in children with suspected genetic disorders. EMHJ 1997;3:114-22.
-
(1997)
EMHJ
, vol.3
, pp. 114-122
-
-
Mokhtar, M.M.1
-
7
-
-
0033174755
-
Chromosome abnormalities in a referred population for suspected chromosomal aberrations: A report of 4117 cases
-
Kim SS, Jung SC, Kim HJ, Moon HR, Lee JS. Chromosome abnormalities in a referred population for suspected chromosomal aberrations: A report of 4117 cases. J Korean Med Sci 1999;14:373-6.
-
(1999)
J Korean Med Sci
, vol.14
, pp. 373-376
-
-
Kim, S.S.1
Jung, S.C.2
Kim, H.J.3
Moon, H.R.4
Lee, J.S.5
-
8
-
-
0035575504
-
Karyotype analysis of 161 unrelated schizophrenics: No increased rates of X chromosome mosaicism or inv (9), using ethnical matched and age-stratified controls
-
Toyota T, Shimizu H, Yamada K, Yoshitsugu K, Meerabux J, Hattori E, et al. Karyotype analysis of 161 unrelated schizophrenics: No increased rates of X chromosome mosaicism or inv (9), using ethnical matched and age-stratified controls. Schizophr Res 2001;52:171-9.
-
(2001)
Schizophr Res
, vol.52
, pp. 171-179
-
-
Toyota, T.1
Shimizu, H.2
Yamada, K.3
Yoshitsugu, K.4
Meerabux, J.5
Hattori, E.6
-
9
-
-
0029268807
-
Pericentric of inversion 9-incidence and clinical significance
-
Teo SH, Tan M, Knight L, Yeo SH, Ng I. Pericentric of inversion 9-incidence and clinical significance. Ann Acad Med Singapore 1995;24:302-4.
-
(1995)
Ann Acad Med Singapore
, vol.24
, pp. 302-304
-
-
Teo, S.H.1
Tan, M.2
Knight, L.3
Yeo, S.H.4
Ng, I.5
-
13
-
-
0031129703
-
Cytogenetic analysis in couples with spontaneous abortions
-
Sasiadek M, Haus O, Lukasik-Majchrowska M, Slezak Paprocka-Borowicz M, Busza H, Plewa R, et al. Cytogenetic analysis in couples with spontaneous abortions. Ginekol Pol 1997;68:248-52.
-
(1997)
Ginekol Pol
, vol.68
, pp. 248-252
-
-
Sasiadek, M.1
Haus, O.2
Lukasik-Majchrowska, M.3
Slezak Paprocka-Borowicz, M.4
Busza, H.5
Plewa, R.6
-
14
-
-
0022469919
-
Six cases of partial duplication-deficiency 21 syndrome: 21(dupq22delp23) due to maternal pericentric inversion: inv(21)(p12;q22). A family study
-
Fraisse J, Philip T, Bertheas MF, Lauras B. Six cases of partial duplication-deficiency 21 syndrome: 21(dupq22delp23) due to maternal pericentric inversion: inv(21)(p12;q22). A family study. Ann Genet 1986;29:177-80.
-
(1986)
Ann Genet
, vol.29
, pp. 177-180
-
-
Fraisse, J.1
Philip, T.2
Bertheas, M.F.3
Lauras, B.4
-
15
-
-
0024412088
-
Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: Data from United States and Canadian laboratories
-
Daniel A, Hook EB and Wulf G. Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: Data from United States and Canadian laboratories. Am J Med Genet 1989;33:14-23.
-
(1989)
Am J Med Genet
, vol.33
, pp. 14-23
-
-
Daniel, A.1
Hook, E.B.2
Wulf, G.3
-
16
-
-
0022645056
-
Synapsis and synaptic adjustment in an infertile human male heterozygous for a pericentric inversion in chromosome 1
-
Gabriel-Robez O, Ratomponirina C, Rumpler Y, Le Marec B, Luciani JM, Guichaoua MR. Synapsis and synaptic adjustment in an infertile human male heterozygous for a pericentric inversion in chromosome 1. Hum Genet 1986;72:148-52.
-
(1986)
Hum Genet
, vol.72
, pp. 148-152
-
-
Gabriel-Robez, O.1
Ratomponirina, C.2
Rumpler, Y.3
Le Marec, B.4
Luciani, J.M.5
Guichaoua, M.R.6
-
17
-
-
0023448280
-
Reproductive failure and pericentric inversion in man
-
Gabriel-Robez O, Ratomponirina C, Croquette M, Maetz JL, Couturier J and Rumpler Y Reproductive failure and pericentric inversion in man. Andrologia 1987;19:662-9.
-
(1987)
Andrologia
, vol.19
, pp. 662-669
-
-
Gabriel-Robez, O.1
Ratomponirina, C.2
Croquette, M.3
Maetz, J.L.4
Couturier, J.5
Rumpler, Y.6
-
18
-
-
0022899131
-
Meiotic behaviour of familial pericentric inversions of chromosomes 1 and 9
-
Guichaoua MR, Gabriel-Robez O, Ratomponirina C, Delafontaine D, Le Marec B, Taillemite JL, et al. Meiotic behaviour of familial pericentric inversions of chromosomes 1 and 9. Ann Genet 1986;29:207-14.
-
(1986)
Ann Genet
, vol.29
, pp. 207-214
-
-
Guichaoua, M.R.1
Gabriel-Robez, O.2
Ratomponirina, C.3
Delafontaine, D.4
Le Marec, B.5
Taillemite, J.L.6
-
19
-
-
0023026187
-
EM investigations of surface spread synaptonemal complexes in a human male carrier of a pericentric inversion inv (13) (p12q14): The role of heterosynapsis for spermatocyte survival
-
Saadallah N, Hulten M. EM investigations of surface spread synaptonemal complexes in a human male carrier of a pericentric inversion inv (13) (p12q14): The role of heterosynapsis for spermatocyte survival. Ann Hum Genet 1986;50:369-83.
-
(1986)
Ann Hum Genet
, vol.50
, pp. 369-383
-
-
Saadallah, N.1
Hulten, M.2
-
20
-
-
0023186887
-
Electron microscopic investigations of synaptonemal complexes in an infertile human male carrier of a pericentric inversion inv(1)(p32q42). Regular loop formation but defective synapsis including a possible interchromosomal effect
-
Batanian J, Hulten MA. Electron microscopic investigations of synaptonemal complexes in an infertile human male carrier of a pericentric inversion inv(1)(p32q42). Regular loop formation but defective synapsis including a possible interchromosomal effect. Hum Genet 1987;76:81-9.
-
(1987)
Hum Genet
, vol.76
, pp. 81-89
-
-
Batanian, J.1
Hulten, M.A.2
-
21
-
-
33747874263
-
Chromosome segregation in an infertile man carrying a unique pericentric inversion, inv(21)(p12q22.3), analysed using fluorescence in situ hybridization on sperm nuclei: Significance for clinical genetics. A case report
-
Malan V, Pipiras E, Sifer C, Kanafani S, Cedrin-Durnerin I, Martin-Pont B, et al. Chromosome segregation in an infertile man carrying a unique pericentric inversion, inv(21)(p12q22.3), analysed using fluorescence in situ hybridization on sperm nuclei: Significance for clinical genetics. A case report. Hum Reprod 2006;21:2052-6.
-
(2006)
Hum Reprod
, vol.21
, pp. 2052-2056
-
-
Malan, V.1
Pipiras, E.2
Sifer, C.3
Kanafani, S.4
Cedrin-Durnerin, I.5
Martin-Pont, B.6
-
22
-
-
0023228455
-
Pericentric inversion in human chromosome 1 and the risk for male sterility
-
Chandley AC, McBeath S, Speed RM, Yorston L, Hargreave TB. Pericentric inversion in human chromosome 1 and the risk for male sterility. J Med Genet 1987;24:325-34.
-
(1987)
J Med Genet
, vol.24
, pp. 325-334
-
-
Chandley, A.C.1
McBeath, S.2
Speed, R.M.3
Yorston, L.4
Hargreave, T.B.5
-
23
-
-
0031753736
-
Pericentric inversion of chromosome 9 in infertile men
-
Sasagawa I, Ishigooka M, Kubota Y, Tomaru M, Hashimoto T, Nakada T. Pericentric inversion of chromosome 9 in infertile men. Int Urol Nephrol 1998;30:203-7.
-
(1998)
Int Urol Nephrol
, vol.30
, pp. 203-207
-
-
Sasagawa, I.1
Ishigooka, M.2
Kubota, Y.3
Tomaru, M.4
Hashimoto, T.5
Nakada, T.6
-
24
-
-
33749822945
-
Observation of an Asperger Syndrome's case with a diagnosis in adulthood and a pericentric inversion chromosome 9
-
Pia Verri A, Cimbro C. Observation of an Asperger Syndrome's case with a diagnosis in adulthood and a pericentric inversion chromosome 9. Minerva Psichiatrica 2002;43:38.
-
(2002)
Minerva Psichiatrica
, vol.43
, pp. 38
-
-
Pia Verri, A.1
Cimbro, C.2
-
25
-
-
0034468140
-
Oculo-auriculo-vertebral (Goldenhar) spectrum associated with pericentric inversion 9: Coincidental findings or ethiologic factor?
-
Stanojevic M, Stipoljev F, Koprcina B, Kurjak A. Oculo-auriculo-vertebral (Goldenhar) spectrum associated with pericentric inversion 9: Coincidental findings or ethiologic factor? J Craniofac Genet Dev Biol 2000;20:150-4.
-
(2000)
J Craniofac Genet Dev Biol
, vol.20
, pp. 150-154
-
-
Stanojevic, M.1
Stipoljev, F.2
Koprcina, B.3
Kurjak, A.4
-
26
-
-
0030791798
-
Ultrastructural sperm defects in two men, carriers of autosomal inversion
-
Baccetti B, Collodel G, Crisa D, Moretti E, Piomboni P. Ultrastructural sperm defects in two men, carriers of autosomal inversion. Andrologia 1997;29:277-82.
-
(1997)
Andrologia
, vol.29
, pp. 277-282
-
-
Baccetti, B.1
Collodel, G.2
Crisa, D.3
Moretti, E.4
Piomboni, P.5
-
27
-
-
0032726797
-
A case of small cerebral cyst and pericentric inversion of chromosome 9 that developed schizophrenia-like psychosis
-
Miyaoka T, Seno H, Itoga M, Ishino H. A case of small cerebral cyst and pericentric inversion of chromosome 9 that developed schizophrenia-like psychosis. Psychiatry Clin Neurosci 1999;53:599-602.
-
(1999)
Psychiatry Clin Neurosci
, vol.53
, pp. 599-602
-
-
Miyaoka, T.1
Seno, H.2
Itoga, M.3
Ishino, H.4
-
28
-
-
0041629067
-
-
Parmar RC, Sira P. Prenatal diagnosis of partial trisomy 21 associated with maternal balanced translocation 46, XX, der 21 t (21q;22q) with pericentric inversion of chromosome 9. J Postgrad Med 2003;49:154-6.
-
Parmar RC, Sira P. Prenatal diagnosis of partial trisomy 21 associated with maternal balanced translocation 46, XX, der 21 t (21q;22q) with pericentric inversion of chromosome 9. J Postgrad Med 2003;49:154-6.
-
-
-
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