R368X mutation in MID1 among recurrent mutations in...

Clinical Dysmorphology 2015 / 01 Vol. 24; Iss. 1

R368X mutation in MID1 among recurrent mutations in patients with X-linked Opitz G/BBB syndrome

Preiksaitiene, Egle, Krasovskaja, Natalija, Utkus, Algirdas, Kasnauskiene, Jurate, Meškienė, Raimonda, Paulauskiene, Iveta, Valevičienė, Nomeda R., Kučinskas, Vaidutis
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Volume:
24
Language:
english
Journal:
Clinical Dysmorphology
DOI:
10.1097/MCD.0000000000000059
Date:
January, 2015
File:
PDF, 483 KB
english, 2015
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