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Volumn 103, Issue 3, 2001, Pages 193-197

Minute supernumerary marker chromosomes identified in two patients with a related, larger pseudodicentric chromosome

(7) Tung, Gloria a Covert, Susan M a Malabed, Katherine L b,c Wohlferd, Monica M c Beckerman, Karen P b Goldberg, James D c Cotter, Philip D a

a CHILDREN S HOSPITAL OAKLAND (United States)

b SAN FRANCISCO GENERAL HOSPITAL (United States)

c UNIVERSITY OF CALIFORNIA (United States)

Author keywords

Chromosome 15; Chromosome 22; Dicentric; Pseudodicentric chromosome; Supernumerary marker chromosome

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 15; CHROMOSOME 22; CHROMOSOME ANALYSIS; CHROMOSOME IDENTIFICATION; CHROMOSOME MOSAICISM; DICENTRIC CHROMOSOME; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; MALE; MARKER CHROMOSOME; PRIORITY JOURNAL; SUPERNUMERARY CHROMOSOME;

AMNIOCENTESIS; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 15; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; FETUS; GENETIC MARKERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; MIDDLE AGED; MOSAICISM; PREGNANCY;

EID: 0035888237 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/ajmg.1565 Document Type: Article

Times cited : (8)

References (31)

1
- 0029875791
- Two supernumerary marker chromosomes, derived from chromosome 6 and 9, in a boy with mild developmental delay
- (1996) Clin Genet , vol.49 , pp. 42-45
- Aalfs, C.M.¹ Jacobs, M.E.² Nieste-Otter, M.A.³ Hennekam, R.C.⁴ Hoovers, J.M.⁵

2
- 0028027588
- Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: Prevalence and characterization by fluorescence in situ hybridization
- (1994) Prenat Diagn , vol.14 , pp. 1019-1028
- Blennow, E.¹ Bui, T.H.² Kristoffersson, U.³ Vujic, M.⁴ Annerén, G.⁵ Holmberg, E.⁶ Nordenskjöld, M.⁷

3
- 0021917574
- Forty four probands with an additional "marker" chromosome
- (1985) Hum Genet , vol.69 , pp. 353-370
- Buckton, K.E.¹ Spowart, G.² Newton, M.S.³ Evans, H.J.⁴

4
- 0021920702
- Multiple congenital anomalies, mental retardation and hypogonadotropic hypogonadism in a boy with small marker chromosomes
- (1985) Am J Med Genet , vol.20 , pp. 607-612
- Copeland, K.C.¹ Hansen, K.² Moore, C.M.³

5
- 0032820496
- Prenatal diagnosis of supernumerary marker 15 chromosomes and exclusion of uniparental disomy for chromosome 15
- (1999) Prenat Diagn , vol.19 , pp. 721-726
- Cotter, P.D.¹ Ledesma, C.T.² Dietz, L.G.³ Pusso, S.⁴ Wohlferd, M.M.⁵ Goldberg, J.D.⁶

6
- 0032477707
- FISH and molecular studies of autosomal supernumerary marker chromosomes excluding those derived from chromosome 15: II. Review of the literature
- (1998) Am J Med Genet , vol.75 , pp. 367-381
- Crolla, J.A.¹

7
- 0028821373
- Supernumerary marker 15 chromosomes: A clinical, molecular and FISH approach to diagnosis and prognosis
- (1995) Hum Genet , vol.95 , pp. 161-170
- Crolla, J.A.¹ Harvey, J.K.² Sitch, F.L.³ Dennis, N.R.⁴

8
- 0030784523
- A molecular and FISH approach to determining karyotype and phenotype correlations in six patients with supernumerary marker(22) chromosomes
- (1997) Am J Med Genet , vol.72 , pp. 440-447
- Crolla, J.A.¹ Howard, P.² Mitchell, C.³ Long, F.L.⁴ Dennis, N.R.⁵

9
- 0027164995
- Infertility in carriers of two bisatellited marker chromosomes
- (1993) Clin Genet , vol.44 , pp. 71-75
- Gentile, M.¹ Susca, F.² Resta, N.³ Stella, A.⁴ Cascone, A.⁵ Guanti, G.⁶

10
- 0031060712
- Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes
- (1997) Hum Genet , vol.99 , pp. 11-17
- Huang, B.¹ Crolla, J.A.² Christian, S.L.³ Wolf-Ledbetter, M.E.⁴ Macha, M.E.⁵ Papenhausen, P.N.⁶ Ledbetter, D.H.⁷

11
- 0024462169
- Stabilization of dicentric chromosomes in Saccharomyces cerevisiae by telomere addition to broken ends or by centromere deletion
- (1989) EMBO J , vol.8 , pp. 247-254
- Jäger, D.¹ Philippsen, P.²

12
- 0028968840
- A search for uniparental disomy in carriers of supernumerary marker chromosomes
- (1995) Eur J Hum Genet , vol.3 , pp. 21-26
- James, R.S.¹ Temple, I.K.² Dennis, N.R.³ Crolla, J.A.⁴

13
- 0028124770
- Interstitial deletions of repetitive DNA blocks in dicentric human Y chromosomes
- (1994) Chromosoma , vol.103 , pp. 324-330
- Köhler, M.R.¹ Vogt, P.H.²

14
- 0023652384
- A genetic analysis of dicentric minichromosomes in Saccharomyces cerevisiae
- (1987) Cell , vol.48 , pp. 801-812
- Koshland, D.¹ Rutledge, L.² Fitzgerald-Hayes, M.³ Hartwell, L.H.⁴

15
- 0030772819
- Rapid identification of multiple supernumerary ring chromosomes with a new FISH technique
- (1997) J Med Genet , vol.34 , pp. 912-916
- Mackie-Ogilvie, C.¹ Waddle, K.² Mandeville, J.³ Seller, M.J.⁴ Docherty, Z.⁵

16
- 0026602327
- Two extra inv dup(15) chromosomes and male infertility: Second case
- (1992) Am J Med Genet , vol.42 , pp. 402-403
- Manenti, E.¹

17
- 0025092790
- Deletion of specific sequences or modification of centromeric chromatin are responsible for Y chromosome centromere inactivation
- (1990) Hum Genet , vol.85 , pp. 491-494
- Maraschio, P.¹ Zuffardi, O.² Caiulo, A.³ Dainotti, E.⁴ Piantanida, M.⁵ Rivera, H.⁶ Tupler, R.⁷

18
- 0022543855
- Infertility associated with two accessory bisatellited chromosomes
- (1986) Hum Genet , vol.73 , pp. 133-136
- Martín-Lucas, M.A.¹ Pérez-Castillo, A.² Abrisqueta, J.A.³

19
- 0023154332
- A patient with extreme variation in number and size of small marker chromosomes
- (1987) Hum Genet , vol.75 , pp. 191-194
- Mascarello, J.T.¹ Jones, M.C.² Chambers, S.R.³

20
- 0031663725
- Cat eye syndrome chromosome breakpoint clustering: Identification of two intervals also associated with 22q11 deletion syndrome breakpoints
- (1998) Cytogenet Cell Genet , vol.81 , pp. 222-228
- McTaggart, K.E.¹ Budarf, M.L.² Driscoll, D.A.³ Emanuel, B.S.⁴ Ferreira, P.⁵ McDermid, H.E.⁶

21
- 0028021562
- Molecular characterization of the marker chromosome associated with cat eye syndrome
- (1994) Am J Hum Genet , vol.55 , pp. 134-142
- Mears, A.J.¹ Duncan, A.M.V.² Budarf, M.L.³ Emanuel, B.S.⁴ Sellinger, B.⁵ Siegel-Bartelt, J.⁶ Greenberg, C.R.⁷ McDermid, H.E.⁸

22
- 0027184219
- Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridization
- (1993) Hum Genet , vol.91 , pp. 589-598
- Plattner, R.¹ Heerema, N.A.² Howard-Peebles, P.N.³ Miles, J.H.⁴ Soukup, S.⁵ Palmer, C.G.⁶

23
- 0032773588
- Simultaneous occurrence of two supernumerary autosomal ring chromosomes r(1) and r(16) in twins
- (1999) J Med Genet , vol.36 , pp. 625-628
- Shanske, A.L.¹ Dowling, P.² Schmidt, R.³ White, B.J.⁴ Russell, B.⁵ Bogdanow, A.⁶ Marion, R.W.⁷

24
- 0022587338
- Dicentric chromosomes and the inactivation of the centromere
- (1986) Hum Genet , vol.72 , pp. 191-195
- Therman, E.¹ Trunca, C.² Kuhn, E.M.³ Sarto, G.E.⁴

25
- 0023837242
- Multiple "marker" chromosomes: A novel cytogenetic finding in a patient with mental retardation and congenital anomalies
- (1988) Am J Med Genet , vol.29 , pp. 355-359
- Tozzi, C.¹ Calvieri, F.² Alesi, L.³ Neri, G.⁴

26
- 0027527478
- Localization of DNA sequences required for human centromere function through an analysis of rearranged Y chromosomes
- (1993) Nat Genet , vol.5 , pp. 368-375
- Tyler-Smith, C.¹ Oakey, R.J.² Larin, Z.³ Fisher, R.B.⁴ Crocker, M.⁵ Affara, N.A.⁶ Ferguson-Smith, M.A.⁷ Muenke, M.⁸ Zuffardi, O.⁹ Jobling, M.A.¹⁰

27
- 0027976191
- Dynamic mosaicism involving an unstable supernumerary der(22) chromosome in cat eye syndrome
- (1994) Am J Med Genet , vol.49 , pp. 77-82
- Urioste, M.¹ Visedo, G.² Sanchís, A.³ Sentís, C.⁴ Villa, A.⁵ Ludeña, P.⁶ Hortigüela, J.L.⁷ Martínez-Frías, M.L.⁸ Fernández-Piqueras, J.⁹

28
- 0004069991
- New York: McGraw-Hill, Inc
- (1994) Human chromosomes. Principles and techniques, 2nd ed. , pp. 6-14
- Verma, R.S.¹ Babu, A.²

29
- 0022539074
- Deletion of the centromere as a mechanism for achieving stability of a dicentric chromosome
- (1986) Cytogenet Cell Genet , vol.42 , pp. 119-122
- Vianna-Morgante, A.M.¹ Rosenberg, C.²

30
- 0028128302
- Inv dup(15) supernumerary marker chromosomes
- (1994) J Med Genet , vol.31 , pp. 585-595
- Webb, T.¹

31
- 0031881661
- A clinical, cytogenetic and molecular study of ten probands with supernumerary inv dup (15) marker chromosomes
- (1998) Clin Genet , vol.53 , pp. 34-43
- Webb, T.¹ Hardy, C.A.² King, M.³ Watkiss, E.⁴ Mitchell, C.⁵ Cole, T.⁶

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.