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Items: 5

1.

Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and review.

Lennon PA, Cooper ML, Peiffer DA, Gunderson KL, Patel A, Peters S, Cheung SW, Bacino CA.

Am J Med Genet A. 2007 Apr 15;143A(8):791-8. Review.

PMID:
17330859
2.

Interstitial "de novo" tandem duplication of 7(q31.1-q35): first reported case.

Zelante L, Croce AI, Grifa A, Notarangelo A, Calvano S.

Ann Genet. 2003 Jan-Mar;46(1):49-52.

PMID:
12818530
3.
5.

An unbalanced autosomal translocation (7;9) associated with feminization.

Crocker M, Coghill SB, Cortinho R.

Clin Genet. 1988 Jul;34(1):70-3.

PMID:
3409542

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