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

Author

: G. TOSUN & Y. SENER

Edition

: 16

Editor

Collation

Subject

Publisher

: Paediatric Dentistry

Year

: 2006

ISBN

Call Number

Summary :
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.

Copies :

No.	Barcode	Location	No. Shelf	Availability
1	08195101	Ruang Referensi - Perpustakaan FKIK	01	TIDAK DIPINJAMKAN

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