262 related articles for article (PubMed ID: 9268108)
1. Proximal interstitial 6q deletion: a recognizable syndrome.
Kumar R; Riordan D; Dawson AJ; Chudley AE
Am J Med Genet; 1997 Aug; 71(3):353-6. PubMed ID: 9268108
[TBL] [Abstract][Full Text] [Related]
2. Interstitial deletion (6)q13q15.
Gershoni-Baruch R; Mandel H; Bar El H; Bar-Nizan N; Borochowitz Z; Dar H
Am J Med Genet; 1996 Apr; 62(4):345-7. PubMed ID: 8723062
[TBL] [Abstract][Full Text] [Related]
3. Deletion of proximal 6q: a clinical report and review of the literature.
Yamamoto Y; Okamoto N; Shiraishi H; Yanagisawa M; Kamoshita S
Am J Med Genet; 1986 Nov; 25(3):467-71. PubMed ID: 3789009
[TBL] [Abstract][Full Text] [Related]
4. Syndrome of proximal interstitial deletion 4p15: report of three cases and review of the literature.
Chitayat D; Ruvalcaba RH; Babul R; Teshima IE; Posnick JC; Vekemans MJ; Scarpelli H; Thuline H
Am J Med Genet; 1995 Jan; 55(2):147-54. PubMed ID: 7717413
[TBL] [Abstract][Full Text] [Related]
5. Distal monosomy of the long arm of chromosome 6 (6q25----6qter) inherited by maternal translocation t(6q;17q).
Oliveira-Duarte MH; Martelli-Soares LR; Sarquis-Cintra T; Machado ML; Lison MP
Ann Genet; 1990; 33(1):56-9. PubMed ID: 2195984
[TBL] [Abstract][Full Text] [Related]
6. Interstitial 6q duplication in an adult male without growth delay or severe mental retardation.
Cappon SL; Duncan AM; Khalifa MM
Med Sci Monit; 2000; 6(3):581-5. PubMed ID: 11208374
[TBL] [Abstract][Full Text] [Related]
7. Subtle overlapping deletions in the terminal region of chromosome 6q24.2-q26: three cases studied using FISH.
Sukumar S; Wang S; Hoang K; Vanchiere CM; England K; Fick R; Pagon B; Reddy KS
Am J Med Genet; 1999 Nov; 87(1):17-22. PubMed ID: 10528241
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Interstitial deletion and ring chromosome derived from 19q. Proximal 19q trisomy phenotype.
Quack B; Van Roy N; Verschraegen-Spae MR; Klein F
Ann Genet; 1992; 35(4):241-4. PubMed ID: 1296524
[TBL] [Abstract][Full Text] [Related]
10. Ophthalmologic abnormalities in a de novo terminal 6q deletion.
Abu-Amero KK; Hellani A; Salih MA; Al Hussain A; al Obailan M; Zidan G; Alorainy IA; Bosley TM
Ophthalmic Genet; 2010 Mar; 31(1):1-11. PubMed ID: 20141352
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Hunter-McAlpine craniosynostosis phenotype associated with skeletal anomalies and interstitial deletion of chromosome 17q.
Thomas JA; Manchester DK; Prescott KE; Milner R; McGavran L; Cohen MM
Am J Med Genet; 1996 Apr; 62(4):372-5. PubMed ID: 8723067
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Interstitial 6q deletion with a Prader-Willi-like phenotype: a new case and review of the literature.
Gilhuis HJ; van Ravenswaaij CM; Hamel BJ; Gabreëls FJ
Eur J Paediatr Neurol; 2000; 4(1):39-43. PubMed ID: 10701104
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Interstitial deletion of the long arm of chromosome 6 associated with absent pulmonary valve.
Horigome H; Takano T; Hirano T; Kajima T; Ohtani S
Am J Med Genet; 1991 Mar; 38(4):608-11. PubMed ID: 2063905
[TBL] [Abstract][Full Text] [Related]
17. Proximal interstitial 1p36 deletion syndrome: the most proximal 3.5-Mb microdeletion identified on a dysmorphic and mentally retarded patient with inv(3)(p14.1q26.2).
Shimojima K; Páez MT; Kurosawa K; Yamamoto T
Brain Dev; 2009 Sep; 31(8):629-33. PubMed ID: 18835671
[TBL] [Abstract][Full Text] [Related]
18. Interstitial 6q deletion: clinical and array CGH characterisation of a new patient.
Le Caignec C; Swillen A; Van Asche E; Fryns JP; Vermeesch JR
Eur J Med Genet; 2005; 48(3):339-45. PubMed ID: 16179229
[TBL] [Abstract][Full Text] [Related]
19. Proximal 6q interstitial deletion without severe mental retardation.
Myers SM; Challman TD
Genet Couns; 2005; 16(3):269-76. PubMed ID: 16259324
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
