Identification of a homozygous one-basepair deletion in exon 14 of the LAMB3 gene in a patient with Herlitz junctional epidermolysis bullosa and prenatal diagnosis in a family at risk for recurrence.
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R. Burgeson | L. Pulkkinen | A. Christiano | D. Gerecke | J. Vailly | J. Uitto | G. Meneguzzi | C. Miquel | J. Ortonne | J P Ortonne | J Vailly | D Gerecke | R E Burgeson | G Meneguzzi