SCOPUS 정보 검색 플랫폼

Annales de Genetique

Volumn 44, Issue 3, 2001, Pages 129-134

Deletion of 2q37 and duplication of 10q24: Two cases in the same family and review of the literature

(6) Wiktor, A a Feldman, G L a,c Bawle, E V a,b Czarnecki, P a,d Conard, J V b Van Dyke, D L a

a HENRY FORD HEALTH SYSTEM (United States)

b CHILDREN'S HOSPITAL OF MICHIGAN (United States)

c WAYNE STATE UNIVERSITY SCHOOL OF MEDICINE (United States)

d GREENWOOD GENETIC CENTER (United States)

Author keywords

2q deletion; Duplication 10q; Fluorescent in situ hybridization (FISH)

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 10Q; CHROMOSOME 2Q; CHROMOSOME DELETION; CHROMOSOME DELETION 2Q; CHROMOSOME DUPLICATION; CHROMOSOME LOSS; CHROMOSOME TRANSLOCATION; CLINICAL FEATURE; CYTOGENETICS; DEVELOPMENTAL DISORDER; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; INFANT; MALE;

EID: 0034767662 PISSN: 00033995 EISSN: None Source Type: Journal
DOI: 10.1016/S0003-3995(01)01083-8 Document Type: Article

Times cited : (4)

References (12)

1
- 0002877957
- An infant with karyotype 46,XX,del(2)(q27) and severe congenital malformations
- (1992) Am. J. Hum. Genet. , vol.51 , Issue.SUPPL. , pp. 301
- Coldwell, J.G.¹ Gucsavas, M.² Say, B.³ Carpenter, N.J.⁴

2
- 0029038024
- Clincal phenotype associated with terminal 2q37 deletion
- (1995) Clin. Genet. , vol.48 , pp. 134-139
- Conrad, B.¹ Dewald, G.² Christensen, E.³ Lopez, M.⁴ Higgins, J.⁵ Pierpont, M.E.⁶

3
- 0031971690
- Distal 10q trisomy syndrome with unusual cardiac and pulmonary abnormalties
- (1998) J. Med. Genet. , vol.35 , pp. 72-74
- Davies, J.¹ Jaffe, A.² Bush, A.³

4
- 0013831027
- 6-12 13-15 translocation and partial 6-12 trisomy (probably 10)
- (1965) Ann. Genet. , vol.8 , pp. 16-20
- De Grouchy, J.¹ Canet, J.²

5
- 0024405541
- Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37)
- (1989) Am. J. Med. Genet. , vol.32 , pp. 350-352
- Gorski, J.L.¹ Cox, B.A.² Kyine, M.³ Uhlmann, W.⁴ Glover, T.W.⁵

6
- 0026733359
- Smallest terminal deletion of the long arm of chromosome 2 in a mildly affected boy
- (1992) Am. J. Med. Genet. , vol.44 , pp. 500-502
- Lin, S.¹ Petty, E.M.² Gibson, L.H.³ Inserra, J.⁴ Seashore, M.R.⁵ Yang-Feng, T.L.⁶

7
- 0029080844
- Albright hereditary osteodystrophy and del(2)(q37.3) in four unrelated individuals
- (1995) Am. J. Med. Genet. , vol.58 , pp. 1-7
- Phelan, M.A.¹ Rogers, R.C.² Clarkspon, K.B.³ Bowyer, F.P.⁴ Levine, M.A.⁵ Estabrooks, L.L.⁶ Severson, M.C.⁷ Dobyns, W.B.⁸

8
- 0000434051
- Deletion of 2q37: A new syndrome?
- (1992) Am. J. Hum. Genet. , vol.51 , Issue.SUPPL. , pp. 310
- Stein, C.K.¹ Del Signore, C.² Bellinger, M.³ Bryke, C.R.⁴

9
- 0020579534
- Partial trisomy 10q in three unrelated patients
- (1983) Ann. Genet. , vol.26 , pp. 79-85
- Taysi, K.¹ Yang, V.² Monaghan, N.³ Beraha, N.⁴

10
- 0027976080
- Terminal deletion of the long arm of chromosome 2 in a premature infant with karyotype:46,XY,del(2)(q37)
- (1994) Am. J. Med. Genet. , vol.49 , pp. 399-401
- Wang, T.¹ Johnston, K.² Hseih, C.³ Dennery, P.A.⁴

11
- 0027517086
- Autopsy findings in a severely affected infant with a 2q terminal deletion
- (1993) Am. J. Med. Genet. , vol.47 , pp. 1099-1103
- Waters, B.L.¹ Allen, E.F.² Gibson, P.C.³ Johnston, T.⁴

12
- 0028813978
- Brachdactyly and mental retardation: An Albright hereditary osteodystrophy-like syndrome localized to 2q37
- (1995) Am. J. Hum. Genet. , vol.56 , pp. 400-407
- Wilson, L.C.¹ Leverton, K.² Oude Luttikhuis, M.E.M.³ Oley, C.A.⁴ Flint, J.⁵ Wolstenholme, J.⁶ Duckett, D.P.⁷ Barrow, M.A.⁸ Leonard, J.V.⁹ Read, A.P.¹⁰ Trembath, R.C.¹¹

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.