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Items: 5

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Functional disomy for Xq26.3-qter in a boy with an unbalanced t(X;21)(q26.3;p11.2) translocation.

Akiyama M, Kawame H, Ohashi H, Tohma T, Ohta H, Shishikura A, Miyata I, Usui N, Eto Y.

Am J Med Genet. 2001 Mar 1;99(2):111-4. Review.

PMID:
11241467
4.

A familial Xp+ chromosome, dup (Xq26.3-->qter).

Vasquez AI, Rivera H, Bobadilla L, Crolla JA.

J Med Genet. 1995 Nov;32(11):891-3.

5.

An atypical case of fragile X syndrome caused by a deletion that includes the FMR1 gene.

Quan F, Zonana J, Gunter K, Peterson KL, Magenis RE, Popovich BW.

Am J Hum Genet. 1995 May;56(5):1042-51.

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