Apert-syndrome-with-glucose-6-phosphate-dehydrogenase-deficiency-a-case-report

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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 : 0.15159797668457 detik