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HOLOPROSENCEPHALY 2 (disorder)
Known as:
HOLOPROSENCEPHALY 2
, HPE2
, Holoprosencephaly Type 2
A rare disorder characterized by the partial separation of the cerebral hemispheres. It is associated with mutations in the SIX3 gene.
National Institutes of Health
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Related topics
Related topics
22 relations
Agenesis of corpus callosum
Arrhinia
Atelencephaly
Autosomal dominant inheritance
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Broader (1)
Holoprosencephaly
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Alobar Holoprosencephaly with Duodenal Atresia: A Case Report
W. Permadi
,
D. Setiawan
,
M. Aziz
,
Yanuarman nbsp
,
A. D. Anwar
,
F. Wirakusumah
Open Journal of Obstetrics and Gynecology
2019
Corpus ID: 201984325
Introduction: Holoprosencephaly (HPE) is the most frequent malformation of the prosencephalon. It represents the absence or…
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1987
1987
Development of the embryonic trisomy 1 mouse.
B. S. Smith
,
J. C. Pettersen
Teratology
1987
Corpus ID: 34173495
Trisomic and normal control embryos 9.5 through 12 gestational days were examined externally and on serial section with standard…
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Review
1985
Review
1985
Agnathia-holoprosencephaly: a developmental field complex involving face and brain. Report of 3 cases.
D. Bixler
,
R. Ward
,
D. Gale
Journal of craniofacial genetics and…
1985
Corpus ID: 13110964
Agnathia-holoprosencephaly (A-H) is a developmental field complex involving a graded series of defects in the jaws, mouth, tongue…
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