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Clinical Dysmorphology|November 21, 1998
Adams-Oliver syndrome associated with cardiovascular malformationsA E Lin, M N Westgate, M E van der Velde, et al.American Journal of Medical Genetics|July 3, 1995
Previously apparently undescribed syndrome: shallow orbits, ptosis, coloboma, trigonocephaly, gyral malformations, and mental and growth retardationJ C Ramer, A E Lin, W B Dobyns, et al.Journal of Medical Genetics|April 3, 2004
A locus for spondylocarpotarsal synostosis syndrome at chromosome 3p14C Steiner, N Ehtesham, K D Taylor, et al.Chest|November 1, 1996
Effect of inhaled salmeterol on sulfur dioxide-induced bronchoconstriction in asthmatic subjectsH Gong, W S Linn, D A Shamoo, et al.Circulation|October 15, 1996
Clinical approach to genetic cardiomyopathy in childrenM L Schwartz, G F Cox, A E Lin, et al.The Journal of Pediatrics|November 1, 1986
Aortic dilation, dissection, and rupture in patients with Turner syndromeA E Lin, B M Lippe, M E Geffner, et al.American Journal of Medical Genetics|May 14, 1999
Cardiovascular malformations: changes in prevalence and birth status, 1972-1990A E Lin, A H Herring, K S Amstutz, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 1, 2017
Imaging in cutis laxa syndrome caused by a dominant negative ALDH18A1 mutation, with hypotheses for intracranial vascular tortuosity and wide perivascular spacesP F Sinnige, C M A van Ravenswaaij-Arts, P Caruso, et al.American Journal of Medical Genetics|April 15, 2000
Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndromeA E Lin, E V Semina, S Daack-Hirsch, et al.Clinical Pediatrics|April 18, 1998
CHARGE association: an update and review for the primary pediatricianK D Blake, S L Davenport, B D Hall, et al.Pageof 9