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A E Lin

Showing results (41-50 of 75) with videos related to

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Ophthalmic Paediatrics and Genetics|June 1, 1990
Persistent hyperplastic primary vitreous with vertical transmissionA E Lin, A W Biglan, K L Garver
American Journal of Medical Genetics|October 1, 1991
Nager acrofacial dysostosis: male-to-male transmission in 2 familiesA S Aylsworth, A E Lin, P A Friedman
Teratology|October 19, 1999
Circumferential abdominal skin defect possibly due to umbilical cord encirclementA E Lin, D R Genest, D L Brown
Clinical Genetics|December 1, 1987
Unusual pedigree patterns in families with spinal muscular atrophyA E Lin, K L Garver, H Wessel, et al.
The American Journal of Cardiology|February 1, 1986
Balloon and blade atrial septostomy facilitated by two-dimensional echocardiographyA E Lin, T G Di Sessa, R G Williams
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.
The Journal of Pediatrics|April 1, 1985
Familial persistent pulmonary hypertensionA E Lin, J R Milley, R Jaffe, 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.
American Journal of Human Genetics|December 1, 1993
Educating the obstetric community through a genetic newsletterA E Lin, B E Braddock, B Thayer, et al.
Pageof 8

Showing results (41-50 of 75) with videos related to

Sort By:
Pageof 8
Ophthalmic Paediatrics and Genetics|June 1, 1990
Persistent hyperplastic primary vitreous with vertical transmissionA E Lin, A W Biglan, K L Garver
American Journal of Medical Genetics|October 1, 1991
Nager acrofacial dysostosis: male-to-male transmission in 2 familiesA S Aylsworth, A E Lin, P A Friedman
Teratology|October 19, 1999
Circumferential abdominal skin defect possibly due to umbilical cord encirclementA E Lin, D R Genest, D L Brown
Clinical Genetics|December 1, 1987
Unusual pedigree patterns in families with spinal muscular atrophyA E Lin, K L Garver, H Wessel, et al.
The American Journal of Cardiology|February 1, 1986
Balloon and blade atrial septostomy facilitated by two-dimensional echocardiographyA E Lin, T G Di Sessa, R G Williams
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.
The Journal of Pediatrics|April 1, 1985
Familial persistent pulmonary hypertensionA E Lin, J R Milley, R Jaffe, 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.
American Journal of Human Genetics|December 1, 1993
Educating the obstetric community through a genetic newsletterA E Lin, B E Braddock, B Thayer, et al.
Pageof 8