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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 19, 2019
The NuRD complex and macrocephaly associated neurodevelopmental disordersTyler Mark Pierson, Maria G Otero, Katheryn Grand, et al.American Journal of Medical Genetics. Part A|September 18, 2009
Genomic duplication of PTPN11 is an uncommon cause of Noonan syndromeJohn M Graham, Nancy Kramer, Bassem A Bejjani, et al.European Journal of Medical Genetics|September 18, 2014
19q13.32 microdeletion syndrome: three new casesAngela Castillo, Nancy Kramer, Charles E Schwartz, et al.American Journal of Medical Genetics. Part A|December 17, 2009
Severe cleidocranial dysplasia and hypophosphatasia in a child with microdeletion of the C-terminal region of RUNX2Areeg H El-Gharbawy, Joseph N Peeden, Ralph S Lachman, et al.Prenatal Diagnosis|April 13, 2012
Male genital abnormalities in intrauterine growth restrictionStefan F Nemec, Ursula Nemec, Peter C Brugger, et al.Prenatal Diagnosis|March 21, 2012
MR imaging of the fetal musculoskeletal systemStefan Franz Nemec, Ursula Nemec, Peter C Brugger, et al.American Journal of Medical Genetics. Part A|August 15, 2006
A previously unreported mutation in a Currarino syndrome kindredRaymond Y Wang, Julie R Jones, Steve Chen, et al.Insights Into Imaging|February 21, 2012
The skeleton and musculature on foetal MRIUrsula Nemec, Stefan F Nemec, Deborah Krakow, et al.American Journal of Medical Genetics. Part A|March 26, 2014
The intellectual disabilities evaluation and advice system (IDEAS): outcome of the first 55 casesAlasdair G W Hunter, John M Graham, Giovanni Neri, et al.Oral Oncology|October 16, 2013
Tailored immunotherapy for HPV positive head and neck squamous cell cancerNeil Gildener-Leapman, John Lee, Robert L FerrisPageof 64