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R E Pyeritz

Showing results (101-110 of 171) with videos related to

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American Journal of Human Genetics|October 1, 1987
The economics of clinical genetics services. II. A time analysis of a medical genetics clinicB A Bernhardt, J Weiner, E C Foster, et al.
The Johns Hopkins Medical Journal|November 1, 1982
Prader--Willi syndrome associated with an interstitial deletion of chromosome 15C M Bonuccelli, G Stetten, R C Levitt, et al.
Nucleic Acids Research|March 11, 1991
Isoleucine397 is changed to threonine in two females with hemophilia BG Sarkar, J D Cassady, R E Pyeritz, et al.
American Journal of Medical Genetics|April 1, 1989
Growth of the foramen magnum in achondroplasiaJ T Hecht, W A Horton, C S Reid, et al.
Radiology|August 1, 1987
Pediatric patients with achondroplasia: CT evaluation of the craniocervical junctionH Wang, A E Rosenbaum, C S Reid, et al.
The Journal of Thoracic and Cardiovascular Surgery|February 1, 1981
Surgical management of patients with the Marfan syndrome and dilatation of the ascending aortaG R McDonald, H V Schaff, R E Pyeritz, et al.
American Journal of Medical Genetics|January 1, 1980
Plasma exchange removes glycosphingolipid in Fabry diseaseR E Pyeritz, M D Ullman, A B Moser, et al.
The Journal of Clinical Ethics|January 1, 1996
Professional healthcare workers' attitudes toward treating patients with multidrug-resistant tuberculosisJ Sugarman, P Terry, R R Faden, et al.
The New England Journal of Medicine|April 24, 1986
Surgical treatment of aneurysms of the ascending aorta in the Marfan syndrome. Results of composite-graft repair in 50 patientsV L Gott, R E Pyeritz, G J Magovern, et al.
Human Mutation|January 1, 1992
Clustering of fibrillin (FBN1) missense mutations in Marfan syndrome patients at cysteine residues in EGF-like domainsH C Dietz, J M Saraiva, R E Pyeritz, et al.
Pageof 18

Showing results (101-110 of 171) with videos related to

Sort By:
Pageof 18
American Journal of Human Genetics|October 1, 1987
The economics of clinical genetics services. II. A time analysis of a medical genetics clinicB A Bernhardt, J Weiner, E C Foster, et al.
The Johns Hopkins Medical Journal|November 1, 1982
Prader--Willi syndrome associated with an interstitial deletion of chromosome 15C M Bonuccelli, G Stetten, R C Levitt, et al.
Nucleic Acids Research|March 11, 1991
Isoleucine397 is changed to threonine in two females with hemophilia BG Sarkar, J D Cassady, R E Pyeritz, et al.
American Journal of Medical Genetics|April 1, 1989
Growth of the foramen magnum in achondroplasiaJ T Hecht, W A Horton, C S Reid, et al.
Radiology|August 1, 1987
Pediatric patients with achondroplasia: CT evaluation of the craniocervical junctionH Wang, A E Rosenbaum, C S Reid, et al.
The Journal of Thoracic and Cardiovascular Surgery|February 1, 1981
Surgical management of patients with the Marfan syndrome and dilatation of the ascending aortaG R McDonald, H V Schaff, R E Pyeritz, et al.
American Journal of Medical Genetics|January 1, 1980
Plasma exchange removes glycosphingolipid in Fabry diseaseR E Pyeritz, M D Ullman, A B Moser, et al.
The Journal of Clinical Ethics|January 1, 1996
Professional healthcare workers' attitudes toward treating patients with multidrug-resistant tuberculosisJ Sugarman, P Terry, R R Faden, et al.
The New England Journal of Medicine|April 24, 1986
Surgical treatment of aneurysms of the ascending aorta in the Marfan syndrome. Results of composite-graft repair in 50 patientsV L Gott, R E Pyeritz, G J Magovern, et al.
Human Mutation|January 1, 1992
Clustering of fibrillin (FBN1) missense mutations in Marfan syndrome patients at cysteine residues in EGF-like domainsH C Dietz, J M Saraiva, R E Pyeritz, et al.
Pageof 18