SCOPUS 정보 검색 플랫폼

American Journal of Medical Genetics

Volumn 109, Issue 1, 2002, Pages 17-21

High risk of malignancy in mosaic variegated aneuploidy syndrome

(5) Jacquemont, Sébastien a Bocéno, Michelle b Rival, Jean Marie b Méchinaud, Françoise a David, Albert a

a Hopital Mere Enfant CHU de Nantes (France)

b NANTES UNIVERSITY HOSPITAL (France)

Author keywords

Mosaicism; Myelodysplasia; Neoplasia; Variegated aneuploidy

Indexed keywords

ACUTE LYMPHOBLASTIC LEUKEMIA; ANEUPLOIDY; ARTICLE; CANCER SUSCEPTIBILITY; CASE REPORT; CHILDHOOD CANCER; CHROMOSOME BREAKAGE; CHROMOSOME MOSAICISM; CLINICAL FEATURE; HUMAN; MALE; MONOSOMY 7; MYELODYSPLASIA; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; ANEUPLOIDY; FATAL OUTCOME; FEMALE; GROWTH DISORDERS; HUMANS; MALE; MICROCEPHALY; MOSAICISM; NEURAL TUBE DEFECTS; SYNDROME;

EID: 0037089953 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/ajmg.10281 Document Type: Article

Times cited : (66)

References (20)

1
- 0033597383
- Normal expression of the Fanconi anemia proteins FAA and FAC and sensitivity to mitomycin C in two patients with Seckel syndrome
- (1999) Am J Med Genet , vol.83 , pp. 388-391
- Abou-Zahr, F.¹ Bejjani, B.² Kruyt, F.A.³ Kurg, R.⁴ Bacino, C.⁵ Shapira, S.K.⁶ Youssoufian, H.⁷

2
- 0027930367
- Optic atrophy, microcephaly, mental retardation and mosaic variegated aneuploidy: A human mitotic mutation
- (1994) Ann Genet , vol.37 , pp. 75-77
- Bitoun, P.¹ Martin-Pont, B.² Tamboise, E.³ Gaudelus, J.⁴

3
- 0023278875
- Do some patients with Seckel syndrome have hematological problems and/or chromosome breakage?
- (1987) Am J Med Genet , vol.27 , pp. 645-649
- Butler, M.G.¹ Hall, B.D.² Maclean, R.N.³ Lozzio, C.B.⁴

4
- 0029839717
- Possible new variant of Nijmegen breakage syndrome
- (1996) Am J Med Genet , vol.65 , pp. 21-26
- Der Kaloustian, V.M.¹ Kleijer, W.² Booth, A.³ Auerbach, A.D.⁴ Mazer, B.⁵ Elliott, A.M.⁶ Abish, S.⁷ Usher, R.⁸ Watters, G.⁹ Vekemans, M.¹⁰ Eydoux, P.¹¹

5
- 0031984710
- Variegated aneuploidy in two siblings: Phenotype, genotype, CENP-E analysis, and literature review
- (1998) Am J Med Genet , vol.75 , pp. 45-51
- Flejter, W.L.¹ Issa, B.² Sullivan, B.A.³ Carey, J.C.⁴ Brothman, A.R.⁵

6
- 0031802203
- Mosaic variegated aneuploidy with multiple congenital abnormalities: Homozygosity for total premature chromatid separation trait
- (1998) Am J Med Genet , vol.78 , pp. 245-249
- Kajii, T.¹ Kawai, T.² Takumi, T.³ Misu, H.⁴ Mabuchi, O.⁵ Takahashi, Y.⁶ Tachino, M.⁷ Nihei, F.⁸ Ikeuchi, T.⁹

7
- 0032952902
- Child with mosaic variegated aneuploidy and embryonal rhabdomyosarcoma
- (1999) Am J Med Genet , vol.82 , pp. 20-24
- Limwongse, C.¹ Schwartz, S.² Bocian, M.³ Robin, N.H.⁴

8
- 0023261643
- Premature centromere division (PCD): A dominantly inherited cytogenetic anomaly
- (1987) Hum Genet , vol.77 , pp. 193-196
- Madan, K.¹ Lindhout, D.² Palan, A.³

9
- 0028949455
- Cytogenetic aspects of Werner's syndrome lymphocyte cultures
- (1995) Mech Ageing Dev , vol.78 , pp. 117-122
- Melaragno, M.I.¹ Pagni, D.² Smith, M.A.³

10
- 0025178665
- Mitotic disturbance associated with mosaic aneuploidies
- (1990) Hum Genet , vol.84 , pp. 361-364
- Miller, K.¹ Muller, W.² Winkler, L.³ Hadam, M.R.⁴ Ehrich, J.H.⁵ Flatz, S.D.⁶

11
- 0006113322
- Recurrent multiple aneuploïdies: A family with autosomal recessive failure of mitotic contrôle
- (1997) J Med Genet , vol.34 , Issue.SUPPL. 1
- Nash, R.N.¹ Willat, L.R.² Andrews, T.³ Green, A.J.⁴

12
- 0017154470
- Trisomy 8 restricted to cultured fibroblast
- (1976) J Med Genet , vol.13 , pp. 229
- Niss, R.¹ Passarge, E.²

13
- 0024335159
- Evidence for a human mitotic mutant with pleiotropic effect
- (1989) Ann Hum Genet , vol.53 , pp. 243-248
- Papi, L.¹ Montali, E.² Marconi, G.³ Guazzelli, R.⁴ Bigozzi, U.⁵ Maraschio, P.⁶ Zuffardi, O.⁷

14
- 0017642705
- Trisomy 8: An international study of 70 patients
- (1977) Birth Defects Orig Artic Ser , vol.13 , Issue.3 C , pp. 171-184
- Ricardi, V.M.¹

15
- 0021015953
- A dominantly inherited cytogenetic anomaly: A possible cell division mutant
- (1983) Hum Genet , vol.65 , pp. 117-121
- Rudd, N.L.¹ Teshima, I.E.² Martin, R.H.³ Sisken, J.E.⁴ Weksberg, R.⁵

16
- 0002992261
- A mititique mutant causing non-disjunction to man
- Berlin
- (1986) Proceedings of the 7th International Congress of Human Genetics , Issue.PART 1 , pp. 163
- Scheres, J.M.¹ Hustinx, T.W.J.² Madan, K.³ Beltman, J.D.⁴ Lindhout, D.⁵

17
- 0028932879
- Seckel syndrome in a family with three affected children and hematological manifestations associated with chromosome instability
- (1995) Genet Couns , vol.6 , pp. 37-41
- Syrrou, M.¹ Georgiou, I.² Paschopoulos, M.³ Lolis, D.⁴

18
- 0023680361
- Siblings with chromosome mosaicism, microcephaly, and growth retardation: The phenotypic expression of a human mitotic mutant?
- (1988) Hum Genet , vol.80 , pp. 197-200
- Tolmie, J.L.¹ Boyd, E.² Batstone, P.³ Ferguson-Smith, M.E.⁴ Al Roomi, L.⁵ Connor, J.M.⁶

19
- 0026323384
- Mosaic variegated aneuploidy with microcephaly: A new human mitotic mutant?
- (1991) Ann Genet , vol.34 , pp. 287-292
- Warburton, D.¹ Anyane-Yeboa, K.² Taterka, P.³ Yu, C.Y.⁴ Olsen, D.⁵

20
- 0028786115
- Constitutional trisomy 8 and myelodysplasia: Report of a case and review of the literature
- (1995) Leuk Res , vol.19 , pp. 733-736
- Zollino, M.¹ Genuardi, M.² Bajer, J.³ Tornesello, A.⁴ Mastrangelo, S.⁵ Zampino, G.⁶ Mastrangelo, R.⁷ Neri, G.⁸

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.