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American Journal of Medical Genetics|May 8, 1999
Cardiac anomalies in the Simpson-Golabi-Behmel syndromeA E Lin, G Neri, R Hughes-Benzie, et al.Journal of Medical Genetics|December 1, 1996
Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22p24)B R Haddad, A E Lin, H Wyandt, et al.American Journal of Medical Genetics|June 28, 2001
Exclusion of growth factor gene mutations as a common cause of Sotos syndromeA E Lin, Q Liu, G B Mannheim, et al.The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|January 1, 1991
The branchio-oculo-facial syndromeA E Lin, H W Losken, R Jaffe, et al.American Journal of Medical Genetics|June 1, 1991
Beemer-Langer syndrome with manifestations of an orofaciodigital syndromeA E Lin, N Doshi, L Flom, et al.American Journal of Diseases of Children (1960)|September 1, 1987
The pattern of cardiovascular malformation in the CHARGE associationA E Lin, A J Chin, W Devine, et al.Journal of the American College of Cardiology|March 1, 1986
Subaortic obstruction in complex congenital heart disease: management by proximal pulmonary artery to ascending aorta end to side anastomosisA E Lin, H Laks, G Barber, et al.American Journal of Medical Genetics|October 23, 1997
Vitamin K deficiency embryopathy: a phenocopy of the warfarin embryopathy due to a disorder of embryonic vitamin K metabolismH Menger, A E Lin, H V Toriello, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 21, 2001
Heterotaxy: associated conditions and hospital-based prevalence in newbornsA E Lin, B S Ticho, K Houde, et al.American Journal of Medical Genetics|January 31, 1997
Cardiovascular malformations in Smith-Lemli-Opitz syndromeA E Lin, H H Ardinger, R H Ardinger, et al.Pageof 6