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Apert syndrome with glucose-6-phosphate dehydrogenase deficiency: a case report
Penulis
: G. TOSUN & Y. SENER
Edisi
: 16
Editor
:
Collation
:
Subyek
:
Penerbit
: Paediatric Dentistry
Tahun
: 2006
ISBN
:
Call Number
:
Ringkasan :
Apert syndrome is characterized by midface hypoplasia, syndactyly of the hands and feet, proptosis of eyes,steep and flat frontal bones, and premature union of cranial sutures.

Daftar copy :
No. Barcode Lokasi No. Rak Ketersediaan
1 08195101 Ruang Referensi - Perpustakaan FKIK 01 TIDAK DIPINJAMKAN

 

Diproses dalam : 0.23555302619934 detik
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