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Volumn 45, Issue 4, 2004, Pages 477-479

Subfertile couple with inv(2),inv(9) and 16qh+

Author keywords

inv(2); inv(9); Miscarriage; Pericentric inversion

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME ANALYSIS; CHROMOSOME INVERSION; FEMALE; FERTILITY; HETEROCHROMATIN; HUMAN; KARYOTYPE; PREGNANCY; PROGENY; RISK ASSESSMENT; SPONTANEOUS ABORTION; SUBFERTILITY;

EID: 10444248920     PISSN: 12341983     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (15)

References (18)
  • 1
    • 0035047313 scopus 로고    scopus 로고
    • Interchromosomal effect leading to an increase in aneuploidy in sperm nuclei in a man heterozygous for pericentric inversion (inv 9) and C-heterochromatin
    • Amiel A, Sardos-Albertini F, Fejgin MD, Sharony R, Diukman R, Bartoov B, 2001. Interchromosomal effect leading to an increase in aneuploidy in sperm nuclei in a man heterozygous for pericentric inversion (inv 9) and C-heterochromatin. J Hum Genet 46: 245-250.
    • (2001) J Hum Genet , vol.46 , pp. 245-250
    • Amiel, A.1    Sardos-Albertini, F.2    Fejgin, M.D.3    Sharony, R.4    Diukman, R.5    Bartoov, B.6
  • 2
    • 0019208936 scopus 로고
    • Study on segregation and risk for abnormal offspring in carriers of pericentric inversion of the (p11-q13) segment of chromosome 2
    • Baccichetti C, Lenzini E, Peserico A, Tenconi R, 1980. Study on segregation and risk for abnormal offspring in carriers of pericentric inversion of the (p11-q13) segment of chromosome 2. Clin Genet 18: 402-407.
    • (1980) Clin Genet , vol.18 , pp. 402-407
    • Baccichetti, C.1    Lenzini, E.2    Peserico, A.3    Tenconi, R.4
  • 3
    • 0030906676 scopus 로고    scopus 로고
    • Chromosome segregation in a man heterozygous for a pericentric inversion, inv (9)(p11q13), analyzed by using sperm karyotyping and two-color fluorescence in situ hybridization
    • Colls P, Blanco J, Martinez-Pasarell O, Vidal F, Egozcue J, Marquez C, Guitart M, Templado C, 1997. Chromosome segregation in a man heterozygous for a pericentric inversion, inv (9)(p11q13), analyzed by using sperm karyotyping and two-color fluorescence in situ hybridization. Hum Genet 99: 761-765.
    • (1997) Hum Genet , vol.99 , pp. 761-765
    • Colls, P.1    Blanco, J.2    Martinez-Pasarell, O.3    Vidal, F.4    Egozcue, J.5    Marquez, C.6    Guitart, M.7    Templado, C.8
  • 4
    • 0031839349 scopus 로고    scopus 로고
    • Detection of a chromosomal aberration in fetuses arising from recurrent spontaneous abortion by comparative genomic hybridization
    • Daniely M, Aviram-Goldring A, Barkai G, Goldman B, 1998. Detection of a chromosomal aberration in fetuses arising from recurrent spontaneous abortion by comparative genomic hybridization. Hum Reprod 13: 805-809.
    • (1998) Hum Reprod , vol.13 , pp. 805-809
    • Daniely, M.1    Aviram-Goldring, A.2    Barkai, G.3    Goldman, B.4
  • 9
    • 0021710068 scopus 로고
    • Pericentric inversions: Problems and significance for clinical genetics
    • Kaiser P, 1984. Pericentric inversions: problems and significance for clinical genetics. Hum Genet 68: 1-47.
    • (1984) Hum Genet , vol.68 , pp. 1-47
    • Kaiser, P.1
  • 10
    • 0032725502 scopus 로고    scopus 로고
    • Rare interstitial deletion (2)(p11.2p13) in a child with pericentric inversion (2)(p11.2q13) of paternal origin
    • Lacbawan FL, White BJ, Anguiano A, Rigdon DT, Ball KD, Bromage GB, et al. 1999. Rare interstitial deletion (2)(p11.2p13) in a child with pericentric inversion (2)(p11.2q13) of paternal origin. Am J Med Genet 87: 139-142.
    • (1999) Am J Med Genet , vol.87 , pp. 139-142
    • Lacbawan, F.L.1    White, B.J.2    Anguiano, A.3    Rigdon, D.T.4    Ball, K.D.5    Bromage, G.B.6
  • 12
    • 0005212337 scopus 로고
    • Pericentric inversion of chromosome 9 and Down's syndrome: A retrospective and prospective family survey
    • Neri G, Tedeschi B, Serra A, Sanfilipo S, 1981. Pericentric inversion of chromosome 9 and Down's syndrome: a retrospective and prospective family survey. Clin Genet 19: 526-527.
    • (1981) Clin Genet , vol.19 , pp. 526-527
    • Neri, G.1    Tedeschi, B.2    Serra, A.3    Sanfilipo, S.4
  • 13
    • 0018165052 scopus 로고
    • Pericentric inversion inv(2) (p11q13) and inv(2)(p13q11) in 2 unrelated families
    • Phillips RB, 1978. Pericentric inversion inv(2) (p11q13) and inv(2)(p13q11) in 2 unrelated families. J Med Genet 15: 388-390.
    • (1978) J Med Genet , vol.15 , pp. 388-390
    • Phillips, R.B.1
  • 14
    • 0020033616 scopus 로고
    • Two pericentric inversions inv(2)(p11q13) and inv(5)(p13q13) in a patient referred for psychiatric problems
    • Romain DR, Chapman CJ, Columbano-Green L, Smythe RH, Gebbie O, 1982. Two pericentric inversions inv(2)(p11q13) and inv(5)(p13q13) in a patient referred for psychiatric problems. J Med Genet 19: 153-155.
    • (1982) J Med Genet , vol.19 , pp. 153-155
    • Romain, D.R.1    Chapman, C.J.2    Columbano-Green, L.3    Smythe, R.H.4    Gebbie, O.5
  • 15
    • 0005151138 scopus 로고
    • Potential effects of pericentric inversion of the heterochromatic region of chromosome 9
    • Serra A, Bova R, 1980. Potential effects of pericentric inversion of the heterochromatic region of chromosome 9. Clin Genet 18: 87.
    • (1980) Clin Genet , vol.18 , pp. 87
    • Serra, A.1    Bova, R.2
  • 16
    • 0025579568 scopus 로고
    • Pericentric inversion of chromosome 9: Prevalence in 300 Down syndrome families and molecular studies of nondisjunction
    • Serra A, Brahe C, Millington-Ward A, Neri G, Tedeschi B, Tassone F, Bova R, 1990. Pericentric inversion of chromosome 9: prevalence in 300 Down syndrome families and molecular studies of nondisjunction. Am J Med. Genet Suppl 7: 162-168.
    • (1990) Am J Med Genet Suppl , vol.7 , pp. 162-168
    • Serra, A.1    Brahe, C.2    Millington-Ward, A.3    Neri, G.4    Tedeschi, B.5    Tassone, F.6    Bova, R.7
  • 17
    • 0019226002 scopus 로고
    • Synaptosomal complexes and associated structures in microspread human spermatocytes
    • Solari AJ, 1980. Synaptosomal complexes and associated structures in microspread human spermatocytes. Chromosoma 81: 315-337.
    • (1980) Chromosoma , vol.81 , pp. 315-337
    • Solari, A.J.1
  • 18
    • 0018670941 scopus 로고
    • C-band polymorphism of chromosomes 1, 9 and 16 in four subgroups of mentally retarded patients and a normal control population
    • Wang HS, Hamerton JL, 1979. C-band polymorphism of chromosomes 1, 9 and 16 in four subgroups of mentally retarded patients and a normal control population. Hum Genet 51: 269-275.
    • (1979) Hum Genet , vol.51 , pp. 269-275
    • Wang, H.S.1    Hamerton, J.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.