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Items: 11

1.

Expansion of the clinical phenotype of the distal 10q26.3 deletion syndrome to include ataxia and hyperemia of the hands and feet.

Lacaria M, Srour M, Michaud JL, Doja A, Miller E, Schwartzentruber J, Goldsmith C, Majewski J; FORGE Canada Consortium, Boycott KM.

Am J Med Genet A. 2017 Jun;173(6):1611-1619. doi: 10.1002/ajmg.a.38231. Epub 2017 Apr 21.

PMID:
28432728
2.

The severe clinical phenotype for a heterozygous Fabry female patient correlates to the methylation of non-mutated allele associated with chromosome 10q26 deletion syndrome.

Hossain MA, Yanagisawa H, Miyajima T, Wu C, Takamura A, Akiyama K, Itagaki R, Eto K, Iwamoto T, Yokoi T, Kurosawa K, Numabe H, Eto Y.

Mol Genet Metab. 2017 Mar;120(3):173-179. doi: 10.1016/j.ymgme.2017.01.002. Epub 2017 Jan 7.

PMID:
28087245
3.

Chromosome 10q26 deletion syndrome: Two new cases and a review of the literature.

Lin S, Zhou Y, Fang Q, Wu J, Zhang Z, Ji Y, Luo Y.

Mol Med Rep. 2016 Dec;14(6):5134-5140. doi: 10.3892/mmr.2016.5864. Epub 2016 Oct 19. Review.

4.

Hearing loss, coloboma and left ventricular enlargement in a boy with an interstitial 10q26 deletion.

Ramos M, Wilkens A, Krantz ID, Wu Y.

Am J Med Genet C Semin Med Genet. 2016 Jun;172(2):109-16. doi: 10.1002/ajmg.c.31496. Epub 2016 Apr 29.

PMID:
27125467
5.

Craniosynostosis in 10q26 deletion patients: A consequence of brain underdevelopment or altered suture biology?

Faria ÁC, Rabbi-Bortolini E, Rebouças MRGO, de S Thiago Pereira ALA, Frasson MGT, Atique R, Lourenço NCV, Rosenberg C, Kobayashi GS, Passos-Bueno MR, Errera FIV.

Am J Med Genet A. 2016 Feb;170A(2):403-409. doi: 10.1002/ajmg.a.37448. Epub 2015 Nov 14.

PMID:
26566760
6.
7.

Identification of a 0.4 Kb deletion region in 10q26 associated with endometrial carcinoma.

Alves M, Carreira I, Liberato P, Ramos S, Mafra M, Inverno AS, Maia AT, Martins AP, Brito M, Monteiro C.

Oncol Rep. 2010 Feb;23(2):519-22.

PMID:
20043116
8.

Small terminal 10q26 deletion in a male patient with Noonan-like stigmata: diagnosis by cytogenetic and FISH analysis.

Lukusa T, Smeets E, Vermeesch JR, Fryns JP.

Genet Couns. 2002;13(4):417-25.

PMID:
12558112
9.

Terminal deletion of chromosome 10q26: delineation of two clinical phenotypes.

Petit P, Devriendt K, Azou M, Gewillig M, Fryns JP.

Genet Couns. 1998;9(4):271-5.

PMID:
9894164
10.

Terminal deletion of chromosome 10q26 due to a paternal translocation [(7;10)(q36;q26)].

Borovik CL, Brunoni D.

Am J Med Genet. 1991 Dec 15;41(4):534-6. No abstract available.

PMID:
1776651
11.

Severe midline fusion defects in a newborn with 10q26----qter deletion.

Fryns JP, Kleczkowska A, Fivez H, Van den Berghe H.

Ann Genet. 1989;32(2):124-5.

PMID:
2757362

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