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Biblio

Found 3 results

2010
Li F, Shen Y, Köhler U, Sharkey FH, Menon D, Coulleaux L, Malan V, Rio M, McMullan DJ, Cox H et al..  2010.  Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant? European journal of medical genetics. 53(2):93-9. Abstract
2008
Mardo V, Squibb EE, Braverman N, Hoover-Fong JE, Migeon C, Batista DAS, Thomas GH.  2008.  Molecular cytogenetic analysis of a de novo interstitial deletion of chromosome 10q (q25.3q26.13) in a male child with ambiguous genitalia: Evidence for a new critical region for genital development.. American journal of medical genetics. Part A. 146A(17):2293-7.
Lisi EC, Hamosh A, Doheny KF, Squibb E, Jackson B, Galczynski R, Thomas GH, Batista DAS.  2008.  3q29 interstitial microduplication: a new syndrome in a three-generation family.. American journal of medical genetics. Part A. 146A(5):601-9. Abstract

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