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A Rare Combination of Functional Disomy Xp, Deletion Xq13.2-q28 Spanning the XIST Gene, and Duplication 3q25.33-q29 in a Female with der(X)t(X;3)(q13.2;q25.33).
J Pediatr Genet
; 7(1): 23-28, 2018 Mar.
Article
in English
| MEDLINE | ID: mdl-29441218
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