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Patients within the broad holoprosencephaly spectrum have distinct and subtle ophthalmologic anomalies: Response to Khan

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Year: 2012
Type: article
Source: American Journal of Medical Genetics Part A
DOI: 10.1002/ajmg.a.35207
Authors: Daniel E. Pineda‐Alvarez, Benjamin D. Solomon, Erich Roessler, Joan Z. Balog, Donald W. Hadley, Wadih M. Zein, Brian P. Brooks, Maximilian Muenke
Institutions: National Institutes of Health, National Human Genome Research Institute, National Eye Institute
Language: English

Topic: Fetal and Pediatric Neurological Disorders
Subfield: Pediatrics, Perinatology and Child Health
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: green

Funders: National Institutes of Health, National Human Genome Research Institute
Award: Genetics of Brain Development
OpenAlex ID: W2003418010
FWCI:
Cites: 18
Cited by:
Related to: 10
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