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IRIDOGONIODYSGENESIS, TYPE 2
Known as:
Iridogoniodysgenesis type 2
, Iris Hypoplasia With Early-Onset Glaucoma, Autosomal Dominant
, ASGD4
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National Institutes of Health
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Related topics
Related topics
7 relations
Broader (5)
Anterior chamber of eye structure
Eye Abnormalities
Glaucoma
Iris Diseases
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PITX2 gene
PITX2 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Mémoires embarquées non volatiles à grille flottante : challenges technologiques et physiques pour l’augmentation des performances vers le noeud 28nm
Adam Dobri
2017
Corpus ID: 194018581
Les memoires flash sont integrees dans presque tous les aspects de la vie moderne car leurs uns et zeros representent les donnees…
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2013
2013
High school learners' mental construction during solving optimisation problems in Calculus: a South African case study
D. Brijlall
,
Zanele Ndlovu
2013
Corpus ID: 55543911
This qualitative case study in a rural school in Umgungundlovu District in KwaZulu-Natal, South Africa, explored Grade 12…
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2013
2013
Inherited GPI-Anchor Deficiencies Caused By The Hypomorphic Mutations In PIG A gene: Comparison To Paroxysmal Nocturnal Hemogrobinuria
Y. Murakami
,
Mitsuhiro Kato
,
+11 authors
T. Kinoshita
2013
Corpus ID: 208423554
Glycosylphosphatidylinositol (GPI) is a glycolipid that anchors 150 or more kinds of proteins to the cell surface. There are at…
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2012
2012
The Impact of Patient-Prescriber Interaction Group Discussions on Injection Prescribing in Public and Private Primary Health Care Facilities in Kinondoni District, Dar es Salaam, Tanzania
A. Massele
,
Y. Mashalla
,
N. Mwamba
2012
Corpus ID: 73989053
The use of medicine in treating diseases is an integral component of health care, and currently practicing physicians are being…
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2008
2008
Iridogoniodysgenesis syndrome: a case report.
T. Knežević
,
K. Novak-Lauš
,
J. Škunca
,
Z. Mandić
Acta Clinica Croatica
2008
Corpus ID: 6645250
A rare case is presented of iridogoniodysgenesis syndrome, an autosomal dominant inheritance disorder that includes abnormalities…
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2002
2002
New home for PACT and IGDS : Recrutment Supplement
J. Love
2002
Corpus ID: 113524694
This article describes how the school of chemical engineering and advanced materials at Newcastle University is providing new…
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2000
2000
Cloning, characterization, localization, and mutational screening of the human BARX1 gene.
D. Gould
,
M. Walter
Genomics
2000
Corpus ID: 13141035
The Bar subclass of homeodomain proteins was first identified for its role in Drosophila eye development. The Bar subclass…
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Review
2000
Review
2000
Axenfeld-Rieger syndrome in the age of molecular genetics.
W. Alward
American journal of ophthalmology-glaucoma
2000
Corpus ID: 1452913
1999
1999
Histopathology and molecular basis of iridogoniodysgenesis syndrome.
W. Pearce
,
B. Mielke
,
S. Kulak
,
M. Walter
Ophthalmic Genetics
1999
Corpus ID: 22418699
Iridogoniodysgenesis is an autosomal dominant disorder in which there are abnormalities in the development of the iris stroma and…
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