SCOPUS 정보 검색 플랫폼

Journal of Medical Genetics

Volumn 38, Issue 11, 2001, Pages 740-744

High resolution comparative genomic hybridisation in clinical cytogenetics

(3) Kirchhoff, M a Rose, H a Lundsteen, C a

a Rigshospitalet (Denmark)

Author keywords

Chromosome aberrations; Chromosome analysis; Comparative genomic hybridisation; Dysmorphism

Indexed keywords

ARTICLE; CHILD; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME TRANSLOCATION; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; CYTOGENETICS; DIGEORGE SYNDROME; FETUS; GENE DELETION; GENE DUPLICATION; HUMAN; HUMAN CELL; HUMAN TISSUE; KARYOTYPE; MAJOR CLINICAL STUDY; MENTAL DEFICIENCY; PRADER WILLI SYNDROME; PRIORITY JOURNAL; WILLIAMS BEUREN SYNDROME;

EID: 0034754559 PISSN: 00222593 EISSN: None Source Type: Journal
DOI: 10.1136/jmg.38.11.740 Document Type: Article

Times cited : (111)

References (28)

1
- 0031839349
- Detection of chromosomal aberration in fetuses arising from recurrent spontaneous abortion by comparative genomic hybridization
- (1998) Hum Reprod , vol.13 , pp. 805-809
- Daniely, M.¹ Aviram-Goldring, A.² Barkai, G.³ Goldman, B.⁴

2
- 0032195407
- Clinical applications of comparative genomic hybridization
- (1998) Genet Med , vol.1 , pp. 4-12
- Levy, B.¹ Dunn, T.M.² Kaffe, S.³ Kardon, N.⁴ Hirschhorn, K.⁵

3
- 0034047585
- Molecular cytogenetic studies in three patients with partial trisomy 2p, including CGH from paraffin-embedded tissue
- (2000) Am J Med Genet , vol.91 , pp. 74-82
- Airam-Goldring, A.¹ Fritz, B.² Bartsch, C.³ Steuber, E.⁴ Daniely, M.⁵ Lev, D.⁶ Chaki, R.⁷ Barkai, G.⁸ Frydman, M.⁹ Rehder, H.¹⁰

4
- 0033924465
- Comparative genomic hybridization for cytogenetic evaluation of stillbirth
- (2000) Obstet Gynecol , vol.96 , pp. 281-286
- Christianes, C.G.¹ Vissers, J.² Poddighe, P.J.³ De Pater, J.M.⁴

5
- 0033974777
- Analysis of uncultured amniocytes by comparative genomic hybridization: A prospective prenatal study
- (2000) Prenat Diagn , vol.20 , pp. 123-131
- Lapierre, J.M.¹ Cacheux, V.² Luton, D.³ Collot, N.⁴ Oury, J.F.⁵ Aurias, A.⁶ Tachdjian, G.⁷

6
- 0034608277
- Comparative genomic hybridization: A new approach to screening for intrauterine complete or mosaic aneuploidy
- (2000) Am J Med Genet , vol.92 , pp. 281-284
- Lestou, V.S.¹ Desilets, V.² Lomax, B.L.³ Barrett, I.J.⁴ Wilson, R.D.⁵ Langlois, S.⁶ Kalousek, D.K.⁷

7
- 0033926516
- Comparative genomic hybridization in combination with flow cytometry improves results of cytogenetic analysis of spontaneous abortions
- (2000) Am J Hum Genet , vol.66 , pp. 1516-1521
- Lomax, B.¹ Tang, S.² Separovic, E.³ Phillips, D.⁴ Hillard, E.⁵ Thomson, T.⁶ Kalousek, D.K.⁷

8
- 0001584542
- CGH as a routine procedure in a clinical cytogenetic laboratory: A one-year assessment
- (2000) Am J Hum Genet Suppl , vol.67 , pp. 152
- Turleau, C.¹ Lapierre, J.M.² Joly, G.³ Prieur, O.⁴ Raoul, O.⁵ De Blois, M.C.⁶ Morichon-Devallez, N.⁷ Gosset, P.⁸ Romana, S.⁹ Vekemans, M.¹⁰

9
- 0031011310
- Automatic correction of the interfering effect of unsuppressed interspersed repetitive sequences in comparative genomic hybridization analysis
- (1997) Cytometry , vol.28 , pp. 130-134
- Kirchhoff, M.¹ Gerdes, T.² Maahr, J.³ Rose, H.⁴ Lundsteen, C.⁵

10
- 0032032471
- Detection of chromosomal gains and losses in comparative genomic hybridization analysis based on standard reference intervals
- (1998) Cytometry , vol.31 , pp. 163-173
- Kirchhoff, M.¹ Gerdes, T.² Rose, H.³ Maahr, J.⁴ Ottesen, A.M.⁵ Lundsteen, C.⁶

11
- 0032792821
- Deletions below 10 megabasepairs are detected in comparative genomic hybridization by standard reference intervals
- (1999) Genes Chrom Cancer , vol.25 , pp. 410-413
- Kirchhoff, M.¹ Gerdes, T.² Maahr, J.³ Rose, H.⁴ Bentz, M.⁵ Döhner, H.⁶ Lundsteen, C.⁷

12
- 0033822498
- High resolution comparative genomic hybridisation analysis reveals imbalances in dysmorphic patients with normal or apparently balanced karyotypes
- (2000) Eur J Hum Genet , vol.8 , pp. 661-668
- Kirchhoff, M.¹ Rose, H.² Maahr, J.³ Gerdes, T.⁴ Bugge, M.⁵ Tommerup, N.⁶ Tümer, Z.⁷ Lespinasse, J.⁸ Jensen, P.K.A.⁹ Wirth, J.¹⁰ Lundsteen, C.¹¹

13
- 0019452916
- Two unusual G-band variants of the short arm of chromosome 9
- (1981) Clin Genet , vol.19 , pp. 331-334
- Sutherland, G.R.¹ Eyre, H.²

14
- 0032908833
- Amplification of a pseudogene cassette underlies euchromatic variation of 16p at the cytogenetic level
- (1999) Hum Genet , vol.104 , pp. 211-218
- Barber, J.C.K.¹ Reed, C.J.² Dahoun, S.P.³ Joyce, C.A.⁴

15
- 0031767480
- Neurofibromatosis pseudogene amplification underlies euchromatic cytogenetic duplications and triplications of proximal 15q
- (1998) Hum Genet , vol.103 , pp. 600-607
- Barber, J.C.K.¹ Cross, I.E.² Douglas, F.³ Nicholson, J.C.⁴ Moore, K.J.⁵ Browne, C.E.⁶

16
- 0031444629
- Inherited interstitial duplications of proximal 15q: Genotype-phenotype correlations
- (1997) Am J Hum Genet , vol.61 , pp. 1342-1352
- Browne, C.E.¹ Dennis, N.R.² Maher, E.³ Long, F.L.⁴ Nicholson, J.C.⁵ Sillibourne, J.⁶ Barber, J.C.K.⁷

17
- 0025954480
- Absence of predictable phenotypic expression in proximal 15q duplications
- (1991) Clin Genet , vol.40 , pp. 194-201
- Ludowese, C.J.¹ Thompson, K.J.² Sekhon, G.S.³ Pauli, R.M.⁴

18
- 0028798545
- The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation
- (1995) Nat Genet , vol.9 , pp. 132-140
- Flint, J.¹ Wilkie, A.O.² Buckle, V.J.³ Winter, R.M.⁴ Holland, A.J.⁵ McDermid, H.E.⁶

19
- 0002425517
- Subtelomeric rearrangements detected by FISH in patients with idiopathic mental retardation
- (1999) Am J Hum Genet Suppl , vol.65
- Anderlid, B.¹ Annerén, G.² Blennow, E.³ Nordenskjold, M.⁴

20
- 0033552424
- Subtle chromosomal rearrangements in children with unexplained mental retardation
- (1999) Lancet , vol.354 , pp. 1676-1681
- Knight, S.J.¹ Regan, R.² Nicod, A.³ Horsley, S.W.⁴ Kearney, L.⁵ Homfray, T.⁶ Winter, R.M.⁷ Bolton, P.⁸ Flint, J.⁹

21
- 85036978056
- Subtelomeric testing for cryptic chromosomal rearrangements in 68 patients with idiopathic mental retardation and dysmorphology
- (2000) Am J Hum Genet Suppl , vol.67 , pp. 162
- Huang, X.L.¹ Wyandt, H.E.² Milunsky, J.M.³

22
- 0002841513
- Screening for subtle structural anomalies by use of subtelomere specific FISH probe set
- (2000) Am J Hum Genet Suppl , vol.67 , pp. 148
- Jalal, S.M.¹ Harwood, A.² Anderson, M.³ Lorentz, C.⁴ Law, M.⁵ Lindor, N.⁶ Karnes, P.⁷ Kulharya, A.⁸ Sekhon, G.⁹ Michels, V.¹⁰

23
- 0034046292
- Perfect endings: A review of subtelomeric probes and their use in clinical diagnosis
- (2000) J Med Genet , vol.37 , pp. 401-409
- Knight, S.¹ Flint, J.²

24
- 0024458678
- "Possibly" de novo translocations: Prenatal risk counseling
- (1989) Am J Obstet Gynecol , vol.161 , pp. 698-702
- Wassman, E.R.¹ Cheyovich, D.L.² Nakahara, Y.³

25
- 0025941775
- De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: Clinical significance and distribution of breakpoints
- (1991) Am J Hum Genet , vol.49 , pp. 995-1013
- Warburton, D.¹

26
- 0031791316
- Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalities
- (1998) Ann Genet , vol.41 , pp. 133-140
- Lapierre, J.M.¹ Cacheux, V.² Collot, N.³ Da Silva, E.⁴ Hervy, N.⁵ Rivet, D.⁶ Romana, S.⁷ Wiss, J.⁸ Benzaken, B.⁹ Aurias, A.¹⁰ Tachdjian, G.¹¹

27
- 0032868065
- Structural unbalanced chromosome rearrangements resolved by comparative genomic hybridization
- (1999) Cytogenet Cell Genet , vol.86 , pp. 51-55
- Daniely, M.¹ Barkai, G.² Goldman, B.³ Aviram-Goldring, A.⁴

28
- 0035050576
- Cryptic familial t(11;18)(q25;q23) incidentally detected by interphase FISH
- (2001) Clin Genet , vol.59 , pp. 279-283
- Schultz, L.N.¹ Schmidt, P.² Tabor, A.³ Bryndorf, T.⁴ Lundsteen, C.⁵

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.