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American Journal of Medical Genetics. Part A|December 11, 2012
Mosaic maternal uniparental disomy of chromosome 15 in Prader-Willi syndrome: utility of genome-wide SNP arrayKosuke Izumi, Avni B Santani, Matthew A Deardorff, et al.
American Journal of Medical Genetics|September 15, 1992
Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndromeD A Driscoll, N B Spinner, M L Budarf, et al.
American Journal of Medical Genetics. Part A|March 9, 2005
The 22q11.2 deletion in African-American patients: an underdiagnosed population?Donna M McDonald-McGinn, Nancy Minugh-Purvis, Richard E Kirschner, et al.
American Journal of Medical Genetics|October 23, 1997
Skeletal anomalies and deformities in patients with deletions of 22q11J E Ming, D M McDonald-McGinn, T E Megerian, et al.
American Journal of Medical Genetics. Part A|June 23, 2021
Nonlethal presentations of CYP26B1-related skeletal anomalies and multiple synostoses syndromeKatheryn Grand, Cara M Skraban, Jennifer L Cohen, et al.
Neurofibromatosis|January 1, 1988
Intracranial visual pathway gliomas in children with neurofibromatosisR J Packer, L T Bilaniuk, B H Cohen, et al.
American Journal of Medical Genetics. Part A|August 6, 2021
Expanding the phenotypic spectrum of Mendelian connective tissue disorders to include prominent kidney phenotypesAlanna Strong, Cara Skraban, Kevin Meyers, et al.
Pediatrics|July 1, 2009
Apolipoprotein E genotype modifies the risk of behavior problems after infant cardiac surgeryJ William Gaynor, Alex S Nord, Gil Wernovsky, et al.
American Journal of Medical Genetics. Part A|March 3, 2015
Chromosome 1p36.22p36.21 duplications/triplication causes Setleis syndrome (focal facial dermal dysplasia type III)David D Weaver, Audrey R Norby, Jill A Rosenfeld, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|July 21, 2006
Velopharyngeal anatomy in 22q11.2 deletion syndrome: a three-dimensional cephalometric analysisRachel A Ruotolo, Nestor A Veitia, Aaron Corbin, et al.
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