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Circulation|October 15, 1996
Clinical approach to genetic cardiomyopathy in childrenM L Schwartz, G F Cox, A E Lin, et al.
American Journal of Medical Genetics|November 1, 1988
Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypesA E Lin, K L Garver, G Diggans, 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.
American Journal of Medical Genetics|March 13, 1995
Further delineation of the branchio-oculo-facial syndromeA E Lin, R J Gorlin, I W Lurie, et al.
American Journal of Medical Genetics|November 15, 2000
Cardiovascular malformations and other cardiovascular abnormalities in neurofibromatosis 1A E Lin, P H Birch, B R Korf, et al.
Molecular Psychiatry|April 17, 2013
Disruption of MBD5 contributes to a spectrum of psychopathology and neurodevelopmental abnormalitiesJ C Hodge, E Mitchell, V Pillalamarri, et al.
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