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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 BrooksJournal 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.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.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.Clinical Dysmorphology|June 7, 2007
Further delineation of interstitial chromosome 6 deletion syndrome and review of the literatureMonica M Zherebtsov, Rachel T Klein, Hana Aviv, et al.American Journal of Medical Genetics. Part A|May 20, 2011
Terminal deletions of the long arm of chromosome X that include the FMR1 gene in female patients: a case seriesNaomi Yachelevich, Julia Klein Gittler, Susan Klugman, et al.Pageof 2