Changing phenotype in Floating-Harbor syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical)
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4. (1974): Case report 2. In (ed): ?Syndrome Identification.? White Plains, NY: National Foundation?March of Dimes 2(1):305.
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2. Benefits of clinical criteria and high-throughput sequencing for diagnosing children with syndromic craniosynostosis;European Journal of Human Genetics;2020-12-07
3. Single Amino Acid Change Underlies Distinct Roles of H2A.Z Subtypes in Human Syndrome;Cell;2019-09
4. Mandibulofacial dysostosis Bauru type: Refining the phenotype;American Journal of Medical Genetics Part A;2017-05-30
5. Chiari I malformation as part of the Floating-Harbor syndrome?;European Journal of Medical Genetics;2016-12
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