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Genetic Counseling (Geneva, Switzerland)|December 3, 2015
ESOPHAGEAL ATRESIA WITH RECURRENT TRACHEOESOPHAGEAL FISTULAS AND MICRODUPLICATION 22q11.23S Puvabanditsin, E Garrow, M February, et al.Acta Paediatrica (Oslo, Norway : 1992)|July 1, 1995
An unusual cause of congenital ascitesS Puvabanditsin, E Garrow, R VizarraGenetic Counseling (Geneva, Switzerland)|May 20, 2016
PARTIAL TRISOMY 4p AND PARTIAL MONOSOMY 13q: CASE REPORT AND A LITERATURE REVIEWS Puvabanditsin, G Herrera-Garcia, N Gengel, et al.Genetic Counseling (Geneva, Switzerland)|February 28, 2018
Osteocraniosplenic Syndrome-Hypomineralized Skull with Gracile Long Bones and Splenic Hypoplasia: A Case Report and Literature ReviewS Puvabanditsin, M February, V D Stefano, et al.The Journal of Cardiovascular Surgery|March 10, 2001
Congenital lobar emphysemaS Puvabanditsin, E Garrow, A Biswas, et al.Pediatric Radiology|April 1, 1997
Group B streptococcal meningitis: a case of transverse myelitis with spinal cord and posterior fossa cystsS Puvabanditsin, E W Wojdylo, E Garrow, et al.Journal of Pediatric Surgery|May 1, 1996
Postnatal intussusception in a premature infant, causing jejunal atresiaS Puvabanditsin, E Garrow, R Samransamraujkit, et al.Journal of the American Academy of Dermatology|February 15, 2001
Junctional epidermolysis bullosa associated with congenital localized absence of skin, and pyloric atresia in two newborn siblingsS Puvabanditsin, E Garrow, D U Kim, et al.Genetic Counseling (Geneva, Switzerland)|September 15, 2006
Otocephaly, and pulmonary malformation association: two case reportsS Puvabanditsin, E Garrow, S Umaru, et al.Annales De Genetique|December 8, 2004
Partial trisomy 8q and partial monosomy 18p: a case reportS Puvabanditsin, E Garrow, F A Rabi, et al.Pageof 128