Figure 1

Partial SHOX duplications associated with various cases of congenital uterovaginal aplasia (MRKH syndrome): A tangible evidence but a puzzling mechanism

Daniel Guerrier* and Karine Morcel

Published: 24 March, 2021 | Volume 4 - Issue 1 | Pages: 001-008

jgmgt-aid1006-t001

Figure 1:

Diagnosis and main clinical features of patients with MRKH syndrome heterozygous for partial SHOX gene duplications. Genetic similarities with the cases previously described by Gervasini and collaborators [30]. All patients showed normal size, weight and BMI for their age.

Read Full Article HTML DOI: 10.29328/journal.jgmgt.1001006 Cite this Article Read Full Article PDF

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