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R W Marion

Showing results (1-10 of 26) with videos related to

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American Journal of Medical Genetics|May 15, 1993
Apparent dominant transmission of the Rubinstein-Taybi syndromeR W Marion, D M Garcia, J B Karasik
American Journal of Medical Genetics|July 24, 1998
Further delineation of the Opitz G/BBB syndrome: report of an infant with complex congenital heart disease and bladder exstrophy, and review of the literatureZ Jacobson, J Glickstein, T Hensle, et al.
American Journal of Medical Genetics|March 1, 1989
Limb deficiency in an infant with Smith-Lemli-Opitz syndromeL P Singer, R W Marion, J K Li
American Journal of Medical Genetics|March 27, 1995
"C" trigonocephaly syndrome: report of a child with agenesis of the corpus callosum and tetralogy of Fallot, and reviewJ Glickstein, J Karasik, D G Caride, et al.
American Journal of Diseases of Children (1960)|July 1, 1986
Human T-cell lymphotropic virus type III (HTLV-III) embryopathy. A new dysmorphic syndrome associated with intrauterine HTLV-III infectionR W Marion, A A Wiznia, G Hutcheon, et al.
American Journal of Medical Genetics|May 2, 1997
The Marshall syndrome: report of a new family and review of the literatureA L Shanske, A Bogdanow, R J Shprintzen, et al.
American Journal of Diseases of Children (1960)|April 1, 1987
Fetal AIDS syndrome score. Correlation between severity of dysmorphism and age at diagnosis of immunodeficiencyR W Marion, A A Wiznia, R G Hutcheon, et al.
American Journal of Diseases of Children (1960)|March 1, 1988
Variable expression in focal dermal hypoplasia. An example of differential X-chromosome inactivationM A Wechsler, C M Papa, F Haberman, et al.
Journal of Child Neurology|July 1, 1987
Computed tomography of the brain in the Smith-Lemli-Opitz syndromeR W Marion, L A Alvarez, Z S Marans, et al.
American Journal of Medical Genetics|August 3, 2001
Hirschsprung disease in an infant with a contiguous gene syndrome of chromosome 13A Shanske, J C Ferreira, J C Leonard, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics|May 15, 1993
Apparent dominant transmission of the Rubinstein-Taybi syndromeR W Marion, D M Garcia, J B Karasik
American Journal of Medical Genetics|July 24, 1998
Further delineation of the Opitz G/BBB syndrome: report of an infant with complex congenital heart disease and bladder exstrophy, and review of the literatureZ Jacobson, J Glickstein, T Hensle, et al.
American Journal of Medical Genetics|March 1, 1989
Limb deficiency in an infant with Smith-Lemli-Opitz syndromeL P Singer, R W Marion, J K Li
American Journal of Medical Genetics|March 27, 1995
"C" trigonocephaly syndrome: report of a child with agenesis of the corpus callosum and tetralogy of Fallot, and reviewJ Glickstein, J Karasik, D G Caride, et al.
American Journal of Diseases of Children (1960)|July 1, 1986
Human T-cell lymphotropic virus type III (HTLV-III) embryopathy. A new dysmorphic syndrome associated with intrauterine HTLV-III infectionR W Marion, A A Wiznia, G Hutcheon, et al.
American Journal of Medical Genetics|May 2, 1997
The Marshall syndrome: report of a new family and review of the literatureA L Shanske, A Bogdanow, R J Shprintzen, et al.
American Journal of Diseases of Children (1960)|April 1, 1987
Fetal AIDS syndrome score. Correlation between severity of dysmorphism and age at diagnosis of immunodeficiencyR W Marion, A A Wiznia, R G Hutcheon, et al.
American Journal of Diseases of Children (1960)|March 1, 1988
Variable expression in focal dermal hypoplasia. An example of differential X-chromosome inactivationM A Wechsler, C M Papa, F Haberman, et al.
Journal of Child Neurology|July 1, 1987
Computed tomography of the brain in the Smith-Lemli-Opitz syndromeR W Marion, L A Alvarez, Z S Marans, et al.
American Journal of Medical Genetics|August 3, 2001
Hirschsprung disease in an infant with a contiguous gene syndrome of chromosome 13A Shanske, J C Ferreira, J C Leonard, et al.
Pageof 3