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

A Grix

Showing results (1-10 of 20) with videos related to

Pageof 2
Sort By:
American Journal of Medical Genetics|October 1, 1982
Malformations in infants of diabetic mothersA Grix
Birth Defects Original Article Series|January 1, 1979
Noonan phenotype with polydactylyA Grix, B D Hall
The American Review of Respiratory Disease|June 1, 1974
Pneumonitis with pleural effusion in children due to Mycoplasma pneumoniaeA Grix, S T Giammona
Birth Defects Original Article Series|January 1, 1982
Patterns of multiple malformations in infants of diabetic mothersA Grix, C Curry, B D Hall
Birth Defects Original Article Series|January 1, 1975
A new familial syndrome with craniofacial abnormalities, osseous defects and mental retardationA Grix, W Blankenship, R Peterson, et al.
Journal of Clinical Ultrasound : JCU|November 1, 1994
Prenatal diagnosis of lissencephaly: Miller-Dieker syndromeJ P McGahan, A Grix, E O Gerscovich
AJR. American Journal of Roentgenology|May 1, 1990
Differentiation of child abuse from osteogenesis imperfectaD S Ablin, A Greenspan, M Reinhart, et al.
American Journal of Medical Genetics|April 1, 1987
Alopecia-anosmia-deafness-hypogonadism syndrome revisited: report of a new caseK Johnston, M Golabi, B Hall, et al.
Journal of Clinical Ultrasound : JCU|January 1, 1989
Arthrogryposis multiplex congenita: prenatal ultrasonographic diagnosisD P Gorczyca, J P McGahan, K K Lindfors, et al.
American Journal of Human Genetics|March 1, 1991
Intermediate hyperhomocysteinemia resulting from compound heterozygosity of methylenetetrahydrofolate reductase mutationsS S Kang, P W Wong, H G Bock, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics|October 1, 1982
Malformations in infants of diabetic mothersA Grix
Birth Defects Original Article Series|January 1, 1979
Noonan phenotype with polydactylyA Grix, B D Hall
The American Review of Respiratory Disease|June 1, 1974
Pneumonitis with pleural effusion in children due to Mycoplasma pneumoniaeA Grix, S T Giammona
Birth Defects Original Article Series|January 1, 1982
Patterns of multiple malformations in infants of diabetic mothersA Grix, C Curry, B D Hall
Birth Defects Original Article Series|January 1, 1975
A new familial syndrome with craniofacial abnormalities, osseous defects and mental retardationA Grix, W Blankenship, R Peterson, et al.
Journal of Clinical Ultrasound : JCU|November 1, 1994
Prenatal diagnosis of lissencephaly: Miller-Dieker syndromeJ P McGahan, A Grix, E O Gerscovich
AJR. American Journal of Roentgenology|May 1, 1990
Differentiation of child abuse from osteogenesis imperfectaD S Ablin, A Greenspan, M Reinhart, et al.
American Journal of Medical Genetics|April 1, 1987
Alopecia-anosmia-deafness-hypogonadism syndrome revisited: report of a new caseK Johnston, M Golabi, B Hall, et al.
Journal of Clinical Ultrasound : JCU|January 1, 1989
Arthrogryposis multiplex congenita: prenatal ultrasonographic diagnosisD P Gorczyca, J P McGahan, K K Lindfors, et al.
American Journal of Human Genetics|March 1, 1991
Intermediate hyperhomocysteinemia resulting from compound heterozygosity of methylenetetrahydrofolate reductase mutationsS S Kang, P W Wong, H G Bock, et al.
Pageof 2