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PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES (disorder)

Known as: Holoprosencephaly 9, HPE9, HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES 
National Institutes of Health

Papers overview

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Highly Cited
2014
Highly Cited
2014
Solitary median maxillary central incisor (SMMCI) is a rare dental anomaly characterized by a symmetric central incisor of normal… Expand
2012
2012
Six3 exerts multiple functions in the development of anterior neural tissue of vertebrate embryos. Whereas complete loss of Six3… Expand
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Highly Cited
2010
Highly Cited
2010
Variation is an intrinsic feature of biological systems, yet developmental biology does not frequently address population-level… Expand
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Highly Cited
2010
Highly Cited
2010
BACKGROUND The Hedgehog (Hh) pathway provides inductive signals critical for developmental patterning of the brain and face. In… Expand
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2008
2008
Holoprosencephaly (HPE) is the most common human congenital forebrain defect, affecting specification of forebrain tissue and… Expand
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Highly Cited
2008
Highly Cited
2008
The putative transcription factor ZIC2 is associated with a defect of forebrain development, known as Holoprosencephaly (HPE), in… Expand
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Highly Cited
2004
Highly Cited
2004
Mutations of the developmental gene Sonic hedgehog (SHH) and alterations of SHH signaling have been associated with… Expand
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Highly Cited
2002
Highly Cited
2002
Holoprosencephaly (HPE) is a condition characterized by a defect in the development of the midline embryonic forebrain. When… Expand
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Highly Cited
2000
Highly Cited
2000
The homeodomain protein TGIF represses transcription in part by recruiting histone deacetylases. TGIF binds directly to DNA to… Expand
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