178 related articles for article (PubMed ID: 2764033)
1. Terminal deletion 4q in a severely retarded boy.
de Michelena MI; Campos PJ
Am J Med Genet; 1989 Jun; 33(2):228-30. PubMed ID: 2764033
[TBL] [Abstract][Full Text] [Related]
2. Proximal 7q interstitial deletion in a severely mentally retarded and mildly abnormal infant.
Gillar PJ; Kaye CI; Ryan SG; Moore CM
Am J Med Genet; 1992 Sep; 44(2):138-41. PubMed ID: 1456281
[TBL] [Abstract][Full Text] [Related]
3. Interstitial deletion of the band 4p15.3 defined by sequential replication banding.
Davies J; Voullaire L; Bankier A
Ann Genet; 1990; 33(2):92-5. PubMed ID: 2241091
[TBL] [Abstract][Full Text] [Related]
4. Unusual chromosomal mosaicism in Wolf-Hirschhorn syndrome: del(4)(p16)/der(4)(qter-q31.3::pter-qter).
Syrrou M; Borghgraef M; Fryns JP
Am J Med Genet; 2001 Dec; 104(3):199-203. PubMed ID: 11754044
[TBL] [Abstract][Full Text] [Related]
5. Interstitial deletion of the distal long arm of chromosome 4, del (4)(q33-q35), in association with paternal balanced translocation.
Mdzin R; Ko C; Abdul Latif Z; Zakaria Z
Singapore Med J; 2008 Nov; 49(11):e336-9. PubMed ID: 19037546
[TBL] [Abstract][Full Text] [Related]
6. Brief cytogenetic case report: a 4.5-year-old girl with deletion 4q syndrome--de novo, 46,XX, del(4) (pter leads to q31:).
Young RS; Palmer CG; Bender HA; Weaver DD; Hodes ME
Am J Med Genet; 1982 May; 12(1):103-7. PubMed ID: 7091193
[No Abstract] [Full Text] [Related]
7. Deletion of the long arm of chromosome 4 [46,XX,del(4)(q31)] in a patient with congenital anomalies.
Back E; Hertel C; Vogel W; Bettecken F; Thiesen M
Ann Genet; 1977 Dec; 20(4):294-6. PubMed ID: 305761
[TBL] [Abstract][Full Text] [Related]
8. Two patients with chromosome 6q terminal deletions with breakpoints at q24.3 and q25.3.
Meng J; Fujita H; Nagahara N; Kashiwai A; Yoshioka Y; Funato M
Am J Med Genet; 1992 Jul; 43(4):747-50. PubMed ID: 1621768
[TBL] [Abstract][Full Text] [Related]
9. Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypes.
Lin AE; Garver KL; Diggans G; Clemens M; Wenger SL; Steele MW; Jones MC; Israel J
Am J Med Genet; 1988 Nov; 31(3):533-48. PubMed ID: 3067575
[TBL] [Abstract][Full Text] [Related]
10. Brief clinical report: interstitial deletion of the long arm of chromosome 4, del(4)(q28-->q31.3).
Copelli S; del Rey G; Heinrich J; Coco R
Am J Med Genet; 1995 Jan; 55(1):77-9. PubMed ID: 7702102
[TBL] [Abstract][Full Text] [Related]
11. A child with multiple congenital anomalies and karyotype 46,XY,del(14)(q31q32.3): further delineation of chromosome 14 interstitial deletion syndrome.
Gorski JL; Uhlmann WR; Glover TW
Am J Med Genet; 1990 Dec; 37(4):471-4. PubMed ID: 2260590
[TBL] [Abstract][Full Text] [Related]
12. Phenotypic variability of del(2) (q22-q23): report of a case with a review of the literature.
Lurie IW; Supovitz KR; Rosenblum-Vos LS; Wulfsberg EA
Genet Couns; 1994; 5(1):11-4. PubMed ID: 8031530
[TBL] [Abstract][Full Text] [Related]
13. Interstitial deletion 13q: further delineation of the syndrome by clinical and high-resolution chromosome analysis of five patients.
Tranebjaerg L; Nielsen KB; Tommerup N; Warburg M; Mikkelsen M
Am J Med Genet; 1988 Apr; 29(4):739-53. PubMed ID: 3400720
[TBL] [Abstract][Full Text] [Related]
14. A specific syndrome due to deletion of the distal long arm of chromosome 1.
Meinecke P; Vögtel D
Am J Med Genet; 1987 Oct; 28(2):371-6. PubMed ID: 3322005
[TBL] [Abstract][Full Text] [Related]
15. Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype.
Piovani G; Borsani G; Bertini V; Kalscheuer VM; Viertel P; Bellotti D; Valseriati D; Barlati S
Eur J Med Genet; 2006; 49(3):215-23. PubMed ID: 16762823
[TBL] [Abstract][Full Text] [Related]
16. Gardner syndrome in a boy with interstitial deletion of the long arm of chromosome 5.
Kobayashi T; Narahara K; Yokoyama Y; Ueyama S; Mohri O; Fujii T; Fujimoto M; Ohtsuki S; Tsuji K; Seino Y
Am J Med Genet; 1991 Dec; 41(4):460-3. PubMed ID: 1776638
[TBL] [Abstract][Full Text] [Related]
17. De novo interstitial deletion q16.2q21 on chromosome 6.
Villa A; Urioste M; Bofarull JM; Martínez-Frías ML
Am J Med Genet; 1995 Jan; 55(3):379-83. PubMed ID: 7726240
[TBL] [Abstract][Full Text] [Related]
18. Interstitial del(13q) associated with blindness and mental retardation.
Juberg RC; Mowrey PN
Am J Med Genet; 1984 Mar; 17(3):609-13. PubMed ID: 6711612
[TBL] [Abstract][Full Text] [Related]
19. Deletion 2q37: an identifiable clinical syndrome with mental retardation and autism.
Galasso C; Lo-Castro A; Lalli C; Nardone AM; Gullotta F; Curatolo P
J Child Neurol; 2008 Jul; 23(7):802-6. PubMed ID: 18658079
[TBL] [Abstract][Full Text] [Related]
20. Interstitial deletion 11q. Case report and review of the literature.
De Pater JM; Ippel PF; Bijlsma JB; Van Nieuwenhuizen O
Genet Couns; 1997; 8(4):335-9. PubMed ID: 9457504
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
