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Journal of Perinatology : Official Journal of the California Perinatal Association|April 30, 2005
Neonatal Gaucher disease presenting as persistent thrombocytopeniaPhilip Roth, Susan Sklower Brooks, Daniel Potaznik, et al.Burns : Journal of the International Society for Burn Injuries|February 24, 2015
Delivery and management of a preterm infant in the burn unit: a multidisciplinary approachOmar Rodriguez, Ruby Cooma, Michael Cooper, et al.Advances in Neonatal Care : Official Journal of the National Association of Neonatal Nurses|July 31, 2015
Emergence of a Genetic Diagnosis: Case Presentation of a Preterm Infant With Cardiofaciocutaneous SyndromeSharon Anderson, Susan Sklower BrooksAdvances in Neonatal Care : Official Journal of the National Association of Neonatal Nurses|September 10, 2016
An Extremely Rare Disorder of Somatic Mosaicism: CLOVES SyndromeSharon Anderson, Susan Sklower BrooksNeonatal Network : NN|July 10, 2013
When the usual symptoms become an unusual diagnosis: a case report of trifunctional protein complexSharon Anderson, Susan Sklower BrooksAmerican Journal of Medical Genetics. Part A|November 22, 2012
A 0.7 Mb de novo duplication at 7q21.3 including the genes DLX5 and DLX6 in a patient with split-hand/split-foot malformationMilen Velinov, Ausaf Ahmad, Brigette Brown-Kipphut, et al.Journal of Child Neurology|August 9, 2018
Further Delineation of Ribose-5-phosphate Isomerase Deficiency: Report of a Third CaseSusan Sklower Brooks, Sharon Anderson, Vikram Bhise, et al.Journal of Pediatric Health Care : Official Publication of National Association of Pediatric Nurse Associates & Practitioners|March 12, 2017
Congenital Glucose-Galactose Malabsorption: A Case ReportSharon Anderson, Soula Koniaris, Baozhong Xin, et al.Cancer Genetics and Cytogenetics|October 24, 2007
Exclusion of APC and VHL gene deletions by array-based comparative hybridization in two patients with microscopically visible chromosomal aberrationsRobert J Wallerstein, Susan Sklower Brooks, Deanna L Streck, et al.American Journal of Medical Genetics. Part A|September 24, 2004
Proteomic studies identified a single nucleotide polymorphism in glyoxalase I as autism susceptibility factorMohammed A Junaid, Dagmar Kowal, Madhabi Barua, et al.Pageof 3