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Similar articles for PubMed (Select 17551325)

1.

Further delineation of interstitial chromosome 6 deletion syndrome and review of the literature.

Zherebtsov MM, Klein RT, Aviv H, Toruner GA, Hanna NN, Brooks SS.

Clin Dysmorphol. 2007 Jul;16(3):135-40. Review.

PMID:
17551325
2.

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 Jul-Sep;48(3):339-45.

PMID:
16179229
3.

Genotype-phenotype correlation in interstitial 6q deletions: a report of 12 new cases.

Rosenfeld JA, Amrom D, Andermann E, Andermann F, Veilleux M, Curry C, Fisher J, Deputy S, Aylsworth AS, Powell CM, Manickam K, Heese B, Maisenbacher M, Stevens C, Ellison JW, Upton S, Moeschler J, Torres-Martinez W, Stevens A, Marion R, Pereira EM, Babcock M, Morrow B, Sahoo T, Lamb AN, Ballif BC, Paciorkowski AR, Shaffer LG.

Neurogenetics. 2012 Feb;13(1):31-47. doi: 10.1007/s10048-011-0306-5. Epub 2012 Jan 5.

PMID:
22218741
4.

Karyotype-phenotype insights from 11q14.1-q23.2 interstitial deletions: FZD4 haploinsufficiency and exudative vitreoretinopathy in a patient with a complex chromosome rearrangement.

Li P, Zhang HZ, Huff S, Nimmakayalu M, Qumsiyeh M, Yu J, Szekely A, Xu T, Pober BR.

Am J Med Genet A. 2006 Dec 15;140(24):2721-9.

PMID:
17103440
5.

Interstitial deletions of chromosome 6q: genotype-phenotype correlation utilizing array CGH.

Klein OD, Cotter PD, Moore MW, Zanko A, Gilats M, Epstein CJ, Conte F, Rauen KA.

Clin Genet. 2007 Mar;71(3):260-6.

PMID:
17309649
6.

Interstitial 6q microdeletion syndrome and epilepsy: a new patient and review of the literature.

Vignoli A, Scornavacca GF, Peron A, La Briola F, Canevini MP.

Am J Med Genet A. 2013 Aug;161A(8):2009-15. doi: 10.1002/ajmg.a.35993. Epub 2013 Jun 21. Review.

PMID:
23794236
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 5;87(1):17-22. Review.

PMID:
10528241
8.

Fine mapping of breakpoints in two unrelated patients with rare overlapping interstitial deletions of 9q with mild dysmorphic features.

Kulharya AS, Flannery DB, Norris K, Lovell C, Levy B, Velagaleti GV.

Am J Med Genet A. 2008 Sep 1;146A(17):2234-41. doi: 10.1002/ajmg.a.32397.

PMID:
18666229
9.

Delineation of the proximal 3q microdeletion syndrome.

Simovich MJ, Bland SD, Peiffer DA, Gunderson KL, Cheung SW, Yatsenko SA, Shinawi M.

Am J Med Genet A. 2008 Jul 1;146A(13):1729-35. doi: 10.1002/ajmg.a.32292. Review.

PMID:
18536049
10.

De novo interstitial deletion q16.2q21 on chromosome 6.

Villa A, Urioste M, Bofarull JM, Martínez-Frías ML.

Am J Med Genet. 1995 Jan 30;55(3):379-83. Review.

PMID:
7726240
11.

Chromosome 6q deletions: a report of two additional cases and a review of the literature.

McLeod DR, Fowlow SB, Robertson A, Samcoe D, Burgess I, Hoo JJ.

Am J Med Genet. 1990 Jan;35(1):79-84. Review.

PMID:
2405671
12.

Proximal interstitial 6q deletion: a recognizable syndrome.

Kumar R, Riordan D, Dawson AJ, Chudley AE.

Am J Med Genet. 1997 Aug 22;71(3):353-6. Review.

PMID:
9268108
13.

Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.

Battaglia A, Hoyme HE, Dallapiccola B, Zackai E, Hudgins L, McDonald-McGinn D, Bahi-Buisson N, Romano C, Williams CA, Brailey LL, Zuberi SM, Carey JC.

Pediatrics. 2008 Feb;121(2):404-10. doi: 10.1542/peds.2007-0929. Erratum in: Pediatrics. 2008 May;121(5):1081. Braley, Lisa L [corrected to Brailey, Lisa L].

PMID:
18245432
14.

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. Review.

PMID:
3067575
15.

Interstitial deletion of chromosome 6q: precise definition of the breakpoints by microdissection, DNA amplification, and reverse painting.

Rubtsov N, Senger G, Kuzcera H, Neumann A, Kelbova C, Junker K, Beensen V, Claussen U.

Hum Genet. 1996 Jun;97(6):705-9.

PMID:
8641683
16.

Interstitial deletion of 18q: comparative genomic hybridization array analysis of 46, XX,del(18)(q21.2.q21.33).

Kato Z, Morimoto W, Kimura T, Matsushima A, Kondo N.

Birth Defects Res A Clin Mol Teratol. 2010 Feb;88(2):132-5. doi: 10.1002/bdra.20633.

PMID:
19813260
17.

Haploinsufficiency of the gene Quaking (QKI) is associated with the 6q terminal deletion syndrome.

Backx L, Fryns JP, Marcelis C, Devriendt K, Vermeesch J, Van Esch H.

Am J Med Genet A. 2010 Feb;152A(2):319-26. doi: 10.1002/ajmg.a.33202.

PMID:
20082458
18.

Specification of small distal 6q deletions in two patients by gene dosage and in situ hybridization study of plasminogen and alpha-L-fucosidase 2.

Narahara K, Tsuji K, Yokoyama Y, Namba H, Murakami M, Matsubara T, Kasai R, Fukushima Y, Seki T, Wakui K, et al.

Am J Med Genet. 1991 Sep 1;40(3):348-53.

PMID:
1951444
19.

Complex MCA/MR syndrome associated with interstitial deletion of the long arm of chromosome 6, del(6)(q25.1-->q27).

Vermeesch JR, Fryns JP.

Am J Med Genet A. 2003 Jul 15;120A(2):299-300. No abstract available.

PMID:
12833421
20.

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.

PMID:
3789009
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