Showing
1 - 1
results of
1
for search '
Van Genderen, M.M
'
Skip to content
Home
Collections
High Impact Articles
Jawi Collection
Malay Medicine
Search Options
UiTM Open Access
Search by UiTM Scopus
Advanced Search
Search by Category
Discovery Service
Sources
UiTM Journals
List UiTM Journal in IR
Statistic
About
Open Access
Creative Commons Licenses
COKI | Malaysia Open Access
Report Technical
User Guide
Contact Us
Search Tips
FAQs
All Fields
Title
Author
Subject
Call Number
ISBN/ISSN
Tag
Find
Advanced
Author
Van Genderen, M.M
Showing
1 - 1
results of
1
for search '
Van Genderen, M.M
'
, query time: 0.04s
Refine Results
Sort
Relevance
Date Descending
Date Ascending
Call Number
Author
Title
1
The Phenotypic and Mutational Spectrum of the FHONDA Syndrome and Oculocutaneous Albinism: Similarities and Differences
by
Arveiler, B.
,
Bagdonaite-Bejaran, L.
,
Bergen, A.A
,
Birk, O.S
,
Blumenfeld, A.
,
De Wit, G.C
,
Florijn, R.J
,
Fulton, A.B
,
Gradstein, L.
,
Kruijt, C.C
,
Lasseaux, E.
,
Perez, Y.
,
Schalij-Delfos, N.E
,
Van
Genderen
,
M.M
,
Yahalom, C.
,
Zanlonghi, X.
Published 2022
Call Number:
Loading...
Located:
Loading...
View Fulltext in Publisher
Article
Search Tools:
Get RSS Feed
—
Email this Search
Related Subjects
Adolescent
Adult
Aged
Albinism, Oculocutaneous
Amino Acid Transport Systems, Neutral
Anterior Eye Segment
Article
Child
Child, Preschool
DNA
DNA Mutational Analysis
Dutchman
FHONDA
FHONDA syndrome
Female
Follow-Up Studies
Fovea Centralis
Foveal hypoplasia
France
Humans
Infant
Israel
Male
Melanin
Middle Aged
Misrouting
Mutation
Netherlands
Phenotype
Retrospective Studies
Loading...