A new recognizable recessive syndrome with distinct dysmorphism, lymphedema and sensorineural hearing loss caused by Carboxypeptidase D mutations

Yazar
Laupheimer, S.
Altunoglu, U.
Bonnard, C.
Reversade, B.
Kayserili, H.
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Bağlantı
http://hdl.handle.net/20.500.12627/152893
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