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You searched for: Author/Creator Lin, Angela E

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1. Clinical practice guidelines for the care of girls and women with Turner syndrome: proceedings from the 2016 Cincinnati International Turner Syndrome Meeting. Issue 3 (September 2017)

2. Genome sequencing reveals a deep intronic splicing ACVRL1 mutation hotspot in Hereditary Haemorrhagic Telangiectasia. Issue 12 (22nd September 2018)

3. Review of the Pathologic Characteristics in Myhre Syndrome: Gain-of-Function Pathogenic Variants in SMAD4 cause a Multisystem Fibroproliferative Response. (November 2022)

4. Twinning and major birth defects, National Birth Defects Prevention Study, 1997–2007. Issue 11 (20th June 2016)