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Allison D. Britt

University of Texas Medical Branch

6

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GH1 C.291 + 34G>C in a Growth Hormone Deficient Pedigree

2021 Journal of the Endocrine Society
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Copy neutral absence of heterozygosity on chromosome 15 distal long arm: A surrogate marker for Prader-Willi/Angelman syndromes?

2021 Molecular Cytogenetics
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Phenotypes Associated with 16p11.2 Copy Number Gains and Losses at a Single Institution.

2020 Labmedicine
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A De novo HDAC2 variant in a patient with features consistent with Cornelia de Lange syndrome phenotype

2019 American Journal of Medical Genetics Part A
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Genotypic and phenotypic variability of 22q11.2 microduplications: An institutional experience

2019 American Journal of Medical Genetics Part A
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