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Clinical Dysmorphology|November 21, 1998
Hemifacial microsomia in a newborn with hypoplastic skin lesions, an eyelid skin tag, and microphthalmia: an unusual presentation of Delleman syndromeJ E Ming, J Katowitz, D M McDonald-McGinn, et al.American Journal of Medical Genetics|March 1, 1989
Prenatal detection of Roberts-SC phocomelia syndrome: report of 2 sibs with characteristic manifestationsD B Robins, R L Ladda, G A Thieme, et al.Pediatric Surgery International|April 12, 2022
Surgical insights and management in patients with the 22q11.2 deletion syndromePatrick E McGovern, T Blaine Crowley, Elaine H Zackai, et al.Radiology|June 1, 1995
Neurofibromatosis type 1: pathologic substrate of high-signal-intensity foci in the brainD P DiPaolo, R A Zimmerman, L B Rorke, et al.Journal of Pediatric Ophthalmology and Strabismus|September 1, 1993
Ankyloblepharon filiforme adnatum in trisomy 18D A Bacal, L B Nelson, E H Zackai, et al.Clinical and Diagnostic Laboratory Immunology|November 5, 1999
Longitudinal analysis of lymphocyte function and numbers in the first year of life in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)K E Sullivan, D McDonald-McGinn, D A Driscoll, et al.American Journal of Medical Genetics. Part A|November 6, 2009
Three patients with oculo-auriculo-vertebral spectrum and microdeletion 22q11.2M Cristina Digilio, Donna M McDonald-McGinn, Carrie Heike, et al.Pediatrics|January 1, 1988
Growth charts for children with Down syndrome: 1 month to 18 years of ageC Cronk, A C Crocker, S M Pueschel, et al.American Journal of Medical Genetics|January 1, 1979
Deletion mapping: further evidence for the location of acid phosphatase (ACP1) within 2p23B S Emanuel, E H Zackai, D C Van Dyke, et al.Brain Research|December 16, 2006
Corpus callosum morphology and ventricular size in chromosome 22q11.2 deletion syndromeAlexei M C Machado, Tony J Simon, Vy Nguyen, et al.Pageof 63