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Volumn 24, Issue 6, 2004, Pages 430-433

Prenatal diagnosis of interstitially satellited 6p

Author keywords

Interstitial NOR; NOR insertion; Nucleolar organizer region; Prenatal diagnosis; Reciprocal translocation; Satellited 6p

Indexed keywords

ADULT; AMNIOCENTESIS; AMNION CELL; CASE REPORT; CHROMOSOME 6P; CHROMOSOME NOR; CHROMOSOME SATELLITE ASSOCIATION; CHROMOSOME TRANSLOCATION 14; CHROMOSOME TRANSLOCATION 6; CONTROLLED STUDY; CYTOGENETICS; DE NOVO STUDY; DISEASE TRANSMISSION; FAMILY HISTORY; FEMALE; FETUS ECHOGRAPHY; GENE INSERTION; GENETIC ANALYSIS; GESTATIONAL AGE; HUMAN; KARYOTYPE 46,XX; LYMPHOCYTE COUNT; PARTIAL TRISOMY; PARTIAL TRISOMY 6P; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; REVIEW; UMBILICAL CORD BLOOD;

EID: 3042740811     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.911     Document Type: Review
Times cited : (10)

References (24)
  • 1
  • 2
    • 0029611142 scopus 로고
    • Ectopic nucleolar organizer regions. A common anomaly revealed by Ag-NOR staining of metaphases from nine cancers
    • Atkin NB, Baker MC. 1995. Ectopic nucleolar organizer regions. A common anomaly revealed by Ag-NOR staining of metaphases from nine cancers. Cancer Genet Cytogenet 85: 129-132.
    • (1995) Cancer Genet Cytogenet , vol.85 , pp. 129-132
    • Atkin, N.B.1    Baker, M.C.2
  • 3
    • 0042055027 scopus 로고
    • Interstitial deletion of 4q35 in a familial satellited 4q in a child with developmental delay
    • Babu VR, Roberson JR, Van Dyke DL, Weiss L. 1987. Interstitial deletion of 4q35 in a familial satellited 4q in a child with developmental delay. Am J Hum Genet 41(Supp.): A113.
    • (1987) Am J Hum Genet , vol.41 , Issue.SUPPL.
    • Babu, V.R.1    Roberson, J.R.2    Van Dyke, D.L.3    Weiss, L.4
  • 5
    • 0008450772 scopus 로고
    • Familial insertion of nucleolar organizer regions and centromere material into the long arm of 11
    • Cosper P, Hicks LC, Finley SC, Davis RO, Carroll AJ. 1985. Familial insertion of nucleolar organizer regions and centromere material into the long arm of 11. Am J Hum Genet 37: A89.
    • (1985) Am J Hum Genet , vol.37
    • Cosper, P.1    Hicks, L.C.2    Finley, S.C.3    Davis, R.O.4    Carroll, A.J.5
  • 6
    • 0003175008 scopus 로고
    • A satellited chromosome 2 detected at prenatal diagnosis
    • Elliott J, Barnes ICS. 1992. A satellited chromosome 2 detected at prenatal diagnosis. J Med Genet 29: 213.
    • (1992) J Med Genet , vol.29 , pp. 213
    • Elliott, J.1    Barnes, I.C.S.2
  • 7
    • 0032972155 scopus 로고    scopus 로고
    • Prenatal diagnosis of a satellited non-acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literature
    • Faivre L, Morichon-Delvallez N, Viot G, et al. 1999. Prenatal diagnosis of a satellited non-acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literature. Prenat Diagn 19: 282-286.
    • (1999) Prenat Diagn , vol.19 , pp. 282-286
    • Faivre, L.1    Morichon-Delvallez, N.2    Viot, G.3
  • 8
    • 0032927467 scopus 로고    scopus 로고
    • Ectopic NORs on human chromosomes 4qter and 8q11: Rare chromosomal variants detected in two families
    • Guttenbach M, Haaf T, Steinlein C, Caesar J, Schinzel A, Schmid M. 1999. Ectopic NORs on human chromosomes 4qter and 8q11: rare chromosomal variants detected in two families. J Med Genet 36: 336-342.
    • (1999) J Med Genet , vol.36 , pp. 336-342
    • Guttenbach, M.1    Haaf, T.2    Steinlein, C.3    Caesar, J.4    Schinzel, A.5    Schmid, M.6
  • 9
    • 0031824551 scopus 로고    scopus 로고
    • An interstitial nucleolus organizer region in the long arm of human chromosome 7: Cytogenetic characterization and familial segregation
    • Guttenbach M, Nassar N, Feichtinger W, et al. 1998. An interstitial nucleolus organizer region in the long arm of human chromosome 7: cytogenetic characterization and familial segregation. Cytogenet Cell Genet 80: 104-112.
    • (1998) Cytogenet Cell Genet , vol.80 , pp. 104-112
    • Guttenbach, M.1    Nassar, N.2    Feichtinger, W.3
  • 10
    • 0003238569 scopus 로고
    • Genotype-phenotype correlation in satellited 1p chromosome: Importance of fluorescence in situ hybridization (FISH) applications
    • Habibian R, Hajianpour MJ, Shaffer LG, Niedenard L, Hajianpour AK. 1994. Genotype-phenotype correlation in satellited 1p chromosome: importance of fluorescence in situ hybridization (FISH) applications. Am J Hum Genet 55(Suppl.): A106.
    • (1994) Am J Hum Genet , vol.55 , Issue.SUPPL.
    • Habibian, R.1    Hajianpour, M.J.2    Shaffer, L.G.3    Niedenard, L.4    Hajianpour, A.K.5
  • 12
    • 0003237139 scopus 로고
    • Six cases of satellited long arm of chromosome 2 detected during prenatal chromosome diagnosis
    • Lamb AN, Pettenati M, Hanna J, et al. 1995. Six cases of satellited long arm of chromosome 2 detected during prenatal chromosome diagnosis. Am J Hum Genet 57(Suppl.): A282.
    • (1995) Am J Hum Genet , vol.57 , Issue.SUPPL.
    • Lamb, A.N.1    Pettenati, M.2    Hanna, J.3
  • 17
    • 0343956508 scopus 로고    scopus 로고
    • Satellited chromosome 10 detected prenatally in fetus andmosaic in a parent
    • O'Malley DP, Diehn T, Bullard B, et al. 1997. Satellited chromosome 10 detected prenatally in fetus and mosaic in a parent. Am J Hum Genet 65(Suppl.): A159.
    • (1997) Am J Hum Genet , vol.65 , Issue.SUPPL.
    • O'Malley, D.P.1    Diehn, T.2    Bullard, B.3
  • 18
    • 0026771543 scopus 로고
    • The presence of interstitial telomeric sequences in constitutional chromosome abnormalities
    • Park VM, Gustashaw KM, Wathen TM. 1992. The presence of interstitial telomeric sequences in constitutional chromosome abnormalities. Am J Hum Genet 50: 914-923.
    • (1992) Am J Hum Genet , vol.50 , pp. 914-923
    • Park, V.M.1    Gustashaw, K.M.2    Wathen, T.M.3
  • 19
    • 0024571836 scopus 로고
    • Nucleolus organizer regions (NORs) inserted in 6q15
    • Prieto F, Badía L, Beneyto M, Palau F. 1989. Nucleolus organizer regions (NORs) inserted in 6q15. Hum Genet 81: 289-290.
    • (1989) Hum Genet , vol.81 , pp. 289-290
    • Prieto, F.1    Badía, L.2    Beneyto, M.3    Palau, F.4
  • 20
    • 0003224221 scopus 로고    scopus 로고
    • Fishing for origin of satellite on the long arm of chromosome 4
    • Shah HO, Verma RS, Conte RA, et al. 1997. Fishing for origin of satellite on the long arm of chromosome 4. Am J Hum Genet 61(Suppl.): A375.
    • (1997) Am J Hum Genet , vol.61 , Issue.SUPPL.
    • Shah, H.O.1    Verma, R.S.2    Conte, R.A.3
  • 21
    • 0034605365 scopus 로고    scopus 로고
    • Segregation of a pure form of spastic paraplegia and NOR insertion into Xq11.2
    • Tamagaki A, Shima M, Tomita R, et al. 2000. Segregation of a pure form of spastic paraplegia and NOR insertion into Xq11.2. Am J Med Genet 94: 5-8.
    • (2000) Am J Med Genet , vol.94 , pp. 5-8
    • Tamagaki, A.1    Shima, M.2    Tomita, R.3
  • 22
    • 0034912676 scopus 로고    scopus 로고
    • Prenatal diagnosis of two rare de novo structural aberrations of the Y chromosome: Cytogenetic and molecular analysis
    • Velissariou V, Antoniadi T, Patsalis P, et al. 2001. Prenatal diagnosis of two rare de novo structural aberrations of the Y chromosome: cytogenetic and molecular analysis. Prenat Diagn 21: 484-487.
    • (2001) Prenat Diagn , vol.21 , pp. 484-487
    • Velissariou, V.1    Antoniadi, T.2    Patsalis, P.3
  • 23
    • 0021145656 scopus 로고
    • A familial insertion involving an active nucleolar organiser within chromosome 12
    • Watt JL, Couzin DA, Lloyd DJ, Stephen GS, McKay E. 1984. A familial insertion involving an active nucleolar organiser within chromosome 12. J Med Genet 21: 379-384.
    • (1984) J Med Genet , vol.21 , pp. 379-384
    • Watt, J.L.1    Couzin, D.A.2    Lloyd, D.J.3    Stephen, G.S.4    McKay, E.5
  • 24
    • 0034790956 scopus 로고    scopus 로고
    • Satellites on the terminal short arm of chromosome 12 (12ps), inherited through several generations in three families: A new variant without phenotypic effect
    • Willatt L, Green AJ, Trump D. 2001. Satellites on the terminal short arm of chromosome 12 (12ps), inherited through several generations in three families: a new variant without phenotypic effect. J Med Genet 38: 723-726.
    • (2001) J Med Genet , vol.38 , pp. 723-726
    • Willatt, L.1    Green, A.J.2    Trump, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.