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Matthew A Deardorff

Showing results (1-10 of 128) with videos related to

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American Journal of Medical Genetics. Part A|August 13, 2016
Tumor screening in Beckwith-Wiedemann syndrome-To screen or not to screen?Jennifer M Kalish, Matthew A Deardorff
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|August 30, 2014
Clinical features, diagnostic criteria, and management of Coffin-Siris syndromeSamantha S Vergano, Matthew A Deardorff
American Journal of Medical Genetics. Part A|September 30, 2004
Ganglioglioma in a Sotos syndrome patient with an NSD1 deletionMatthew A Deardorff, Melissa Maisenbacher, Elaine H Zackai
American Journal of Medical Genetics. Part A|February 5, 2017
The utility of alpha-fetoprotein screening in Beckwith-Wiedemann syndromeKelly A Duffy, Matthew A Deardorff, Jennifer M Kalish
BMC Medicine|February 5, 2011
Another tool in the genome-wide association study arsenal: population-based detection of somatic gene conversionMatthew A Deardorff, Jesus Sainz, Struan F A Grant
Protein Science : a Publication of the Protein Society|September 1, 2016
Structural aspects of HDAC8 mechanism and dysfunction in Cornelia de Lange syndrome spectrum disordersMatthew A Deardorff, Nicholas J Porter, David W Christianson
Human Mutation|December 24, 2015
MESP1 Mutations in Patients with Congenital Heart DefectsPetra Werner, Brande Latney, Matthew A Deardorff, et al.
JIMD Reports|August 13, 2016
Argininosuccinic Acid Lyase Deficiency Missed by Newborn ScreenRebecca D Ganetzky, Emma Bedoukian, Matthew A Deardorff, et al.
Pediatric Dermatology|December 13, 2019
A PIK3CA mutation in an acquired capillary malformationJaclyn Rosenthal, Cathryn Sibbald, Melinda Jen, et al.
Journal of Pediatric Orthopedics|January 10, 2015
Melorheostosis: segmental osteopoikilosis or a separate entity?Muayad Kadhim, Matthew A Deardorff, Holly Dubbs, et al.
Pageof 13

Showing results (1-10 of 128) with videos related to

Sort By:
Pageof 13
American Journal of Medical Genetics. Part A|August 13, 2016
Tumor screening in Beckwith-Wiedemann syndrome-To screen or not to screen?Jennifer M Kalish, Matthew A Deardorff
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|August 30, 2014
Clinical features, diagnostic criteria, and management of Coffin-Siris syndromeSamantha S Vergano, Matthew A Deardorff
American Journal of Medical Genetics. Part A|September 30, 2004
Ganglioglioma in a Sotos syndrome patient with an NSD1 deletionMatthew A Deardorff, Melissa Maisenbacher, Elaine H Zackai
American Journal of Medical Genetics. Part A|February 5, 2017
The utility of alpha-fetoprotein screening in Beckwith-Wiedemann syndromeKelly A Duffy, Matthew A Deardorff, Jennifer M Kalish
BMC Medicine|February 5, 2011
Another tool in the genome-wide association study arsenal: population-based detection of somatic gene conversionMatthew A Deardorff, Jesus Sainz, Struan F A Grant
Protein Science : a Publication of the Protein Society|September 1, 2016
Structural aspects of HDAC8 mechanism and dysfunction in Cornelia de Lange syndrome spectrum disordersMatthew A Deardorff, Nicholas J Porter, David W Christianson
Human Mutation|December 24, 2015
MESP1 Mutations in Patients with Congenital Heart DefectsPetra Werner, Brande Latney, Matthew A Deardorff, et al.
JIMD Reports|August 13, 2016
Argininosuccinic Acid Lyase Deficiency Missed by Newborn ScreenRebecca D Ganetzky, Emma Bedoukian, Matthew A Deardorff, et al.
Pediatric Dermatology|December 13, 2019
A PIK3CA mutation in an acquired capillary malformationJaclyn Rosenthal, Cathryn Sibbald, Melinda Jen, et al.
Journal of Pediatric Orthopedics|January 10, 2015
Melorheostosis: segmental osteopoikilosis or a separate entity?Muayad Kadhim, Matthew A Deardorff, Holly Dubbs, et al.
Pageof 13