Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M J Harrod

Showing results (21-30 of 36) with videos related to

Pageof 4
Sort By:
American Journal of Medical Genetics|August 1, 1986
del(20p) with manifestations of arteriohepatic dysplasiaJ L Byrne, M J Harrod, J M Friedman, et al.
Annals of Internal Medicine|August 1, 1976
Congenital absence of the vagina. The Mayer-Rokitansky-Kuster-Hauser syndromeJ E Griffin, C Edwards, J D Madden, et al.
American Journal of Medical Genetics|June 1, 1984
Genetic heterogeneity in spondyloepiphyseal dysplasia congenitaM J Harrod, J M Friedman, G Currarino, et al.
The New England Journal of Medicine|May 16, 1974
Familial incomplete male pseudohermaphroditism, type 1. Evidence for androgen resistance and variable clinical manifestations in a family with the Reifenstein syndromeJ D Wilson, M J Harrod, J L Goldstein, et al.
Prenatal Diagnosis|January 1, 1986
Anatomic correlates of ultrasonographic prenatal diagnosisJ C Rutledge, A G Weinberg, J M Friedman, et al.
The American Journal of Digestive Diseases|September 1, 1975
Familial pseudomembranous colitis and its relation to lincomycin therapyM J Harrod, M S Brown, A G Weinberg, et al.
Neurology|November 1, 1976
alpha-L-iduronidase deficiency and possible Hurler-Scheie genetic compound. Clinical, pathologic, and biochemical findingsP R Winters, M J Harrod, S A Molenich-Heetred, et al.
Archives of Dermatology|May 1, 1977
A cutaneous marker in the Hunter syndrome a report of four casesS D Prystowsky, I H Maumenee, R G Freeman, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|September 11, 1998
Fryns syndrome: prenatal diagnosis and pathologic correlationJ S Sheffield, D M Twickler, C Timmons, et al.
The New England Journal of Medicine|October 31, 1974
Familial incomplete male pseudohermaphroditism, type 2. Decreased dihydrotestosterone formation in pseudovaginal perineoscrotal hypospadiasP C Walsh, J D Madden, M J Harrod, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics|August 1, 1986
del(20p) with manifestations of arteriohepatic dysplasiaJ L Byrne, M J Harrod, J M Friedman, et al.
Annals of Internal Medicine|August 1, 1976
Congenital absence of the vagina. The Mayer-Rokitansky-Kuster-Hauser syndromeJ E Griffin, C Edwards, J D Madden, et al.
American Journal of Medical Genetics|June 1, 1984
Genetic heterogeneity in spondyloepiphyseal dysplasia congenitaM J Harrod, J M Friedman, G Currarino, et al.
The New England Journal of Medicine|May 16, 1974
Familial incomplete male pseudohermaphroditism, type 1. Evidence for androgen resistance and variable clinical manifestations in a family with the Reifenstein syndromeJ D Wilson, M J Harrod, J L Goldstein, et al.
Prenatal Diagnosis|January 1, 1986
Anatomic correlates of ultrasonographic prenatal diagnosisJ C Rutledge, A G Weinberg, J M Friedman, et al.
The American Journal of Digestive Diseases|September 1, 1975
Familial pseudomembranous colitis and its relation to lincomycin therapyM J Harrod, M S Brown, A G Weinberg, et al.
Neurology|November 1, 1976
alpha-L-iduronidase deficiency and possible Hurler-Scheie genetic compound. Clinical, pathologic, and biochemical findingsP R Winters, M J Harrod, S A Molenich-Heetred, et al.
Archives of Dermatology|May 1, 1977
A cutaneous marker in the Hunter syndrome a report of four casesS D Prystowsky, I H Maumenee, R G Freeman, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|September 11, 1998
Fryns syndrome: prenatal diagnosis and pathologic correlationJ S Sheffield, D M Twickler, C Timmons, et al.
The New England Journal of Medicine|October 31, 1974
Familial incomplete male pseudohermaphroditism, type 2. Decreased dihydrotestosterone formation in pseudovaginal perineoscrotal hypospadiasP C Walsh, J D Madden, M J Harrod, et al.
Pageof 4