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R W Marion

Showing results (11-20 of 26) with videos related to

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American Journal of Medical Genetics|May 16, 1997
Central nervous system anomalies in Seckel syndrome: report of a new family and review of the literatureA Shanske, D G Caride, L Menasse-Palmer, et al.
Prenatal Diagnosis|November 1, 1990
Detection and enumeration of colonic mucosal cells in amniotic fluid using a colon epithelial-specific monoclonal antibodyD Chitayat, R W Marion, L Squillante, et al.
American Journal of Human Genetics|May 1, 1990
Spondyloepiphyseal dysplasia congenita: genetic linkage to type II collagen (COL2AI)I J Anderson, R B Goldberg, R W Marion, et al.
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|April 1, 1997
Hemimaxillofacial dysplasia: a report of two new cases and further delineation of the disorderK Paticoff, R W Marion, R J Shprintzen, et al.
Human Genetics|March 10, 1999
A large Alu-mediated deletion, identified by PCR, as the molecular basis for glycogen storage disease type II (GSDII)M L Huie, A L Shanske, J S Kasper, et al.
American Journal of Medical Genetics|June 27, 2000
Fronto-ocular syndrome: newly recognized trigonocephaly syndromeE N Schneider, A Bogdanow, J T Goodrich, et al.
American Journal of Medical Genetics|November 1, 1988
Aspartylglucosaminuria in a Puerto Rican family: additional features of a panethnic disorderD Chitayat, S Nakagawa, R W Marion, et al.
American Journal of Diseases of Children (1960)|August 1, 1987
Autosomal recessive inheritance in the Setleis bitemporal 'forceps marks' syndromeR W Marion, D Chitayat, R G Hutcheon, et al.
Journal of Medical Genetics|August 28, 1999
Simultaneous occurrence of two supernumerary autosomal ring chromosomes r(1) and r(16) in twinsA L Shanske, P Dowling, R Schmidt, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Elevation of serum beta-hexosaminidase and alpha-D-mannosidase in type 2 Gaucher disease: a clinical and biochemical studyD Chitayat, S Nakagawa, R W Marion, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics|May 16, 1997
Central nervous system anomalies in Seckel syndrome: report of a new family and review of the literatureA Shanske, D G Caride, L Menasse-Palmer, et al.
Prenatal Diagnosis|November 1, 1990
Detection and enumeration of colonic mucosal cells in amniotic fluid using a colon epithelial-specific monoclonal antibodyD Chitayat, R W Marion, L Squillante, et al.
American Journal of Human Genetics|May 1, 1990
Spondyloepiphyseal dysplasia congenita: genetic linkage to type II collagen (COL2AI)I J Anderson, R B Goldberg, R W Marion, et al.
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|April 1, 1997
Hemimaxillofacial dysplasia: a report of two new cases and further delineation of the disorderK Paticoff, R W Marion, R J Shprintzen, et al.
Human Genetics|March 10, 1999
A large Alu-mediated deletion, identified by PCR, as the molecular basis for glycogen storage disease type II (GSDII)M L Huie, A L Shanske, J S Kasper, et al.
American Journal of Medical Genetics|June 27, 2000
Fronto-ocular syndrome: newly recognized trigonocephaly syndromeE N Schneider, A Bogdanow, J T Goodrich, et al.
American Journal of Medical Genetics|November 1, 1988
Aspartylglucosaminuria in a Puerto Rican family: additional features of a panethnic disorderD Chitayat, S Nakagawa, R W Marion, et al.
American Journal of Diseases of Children (1960)|August 1, 1987
Autosomal recessive inheritance in the Setleis bitemporal 'forceps marks' syndromeR W Marion, D Chitayat, R G Hutcheon, et al.
Journal of Medical Genetics|August 28, 1999
Simultaneous occurrence of two supernumerary autosomal ring chromosomes r(1) and r(16) in twinsA L Shanske, P Dowling, R Schmidt, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Elevation of serum beta-hexosaminidase and alpha-D-mannosidase in type 2 Gaucher disease: a clinical and biochemical studyD Chitayat, S Nakagawa, R W Marion, et al.
Pageof 3