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1. Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expression

3. Identifying phenotypic expansions for congenital diaphragmatic hernia plus ( CDH +) using DECIPHER data

4. Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann‐Steiner syndrome

6. What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia

7. Cover Image, Volume 176A, Number 10, October 2018

8. Screening and familial characterization of copy-number variations inNR5A1in 46,XY disorders of sex development and premature ovarian failure

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