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Case Reports in Genetics|October 18, 2012
MOMO Syndrome with Holoprosencephaly and Cryptorchidism: Expanding the Spectrum of the New Obesity SyndromeSheetal Sharda, Inusha Panigrahi, Ram Kumar MarwahaIndian Dermatology Online Journal|October 6, 2017
Autosomal Recessive Cutis Laxa Type II: Report of Novel Mutation in a ChildRakesh Kumar, Sheetal Sharda, Vimlesh Soni, et al.JIMD Reports|April 3, 2013
Defect of cobalamin intracellular metabolism presenting as diabetic ketoacidosis: a rare manifestationSheetal Sharda, Suresh Kumar Angurana, Mandeep Walia, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|April 24, 2014
Hypophosphatemic rickets caused by a novel PHEX gene mutation in an Indian girlDevi Dayal, Sheetal Sharda, Savita Verma Attri, et al.Indian Journal of Pediatrics|August 1, 2006
Hemihyperplasia syndromesAshwin B Dalal, Shubha R Phadke, Mandakini Pradhan, et al.American Journal of Medical Genetics. Part A|November 2, 2022
Expanding the spectrum of ADNP-related disorder-Antenatally diagnosed congenital diaphragmatic hernia and a novel de novo mutation in ADNP genePrashant Asegaonkar, Udhaya Kotecha, Mayuresh Dongre, et al.Journal of Pediatric Genetics|September 15, 2016
An Indian girl with Fanconi-Bickel syndrome without SLC2A2 gene mutationDevi Dayal, Parag Dekate, Sheetal Sharda, et al.Journal of Pediatric Orthopedics|February 23, 2007
Intravenous pamidronate therapy in osteogenesis imperfecta: response to treatment and factors influencing outcomeAnurag Bajpai, Madhulika Kabra, Neerja Gupta, et al.Pediatric Dermatology|March 5, 2010
A newborn with acanthosis nigricans: can it be Crouzon syndrome with acanthosis nigricans?Sheetal Sharda, Inusha Panigrahi, Kirti Gupta, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|September 14, 2013
Zellweger syndrome: prenatal and postnatal growth failure with epiphyseal stipplingSuresh Kumar, Renu Suthar, Sheetal Sharda, et al.Pageof 3