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

J Charrow

Showing results (31-40 of 47) with videos related to

Pageof 5
Sort By:
American Journal of Medical Genetics|September 1, 1987
Uncombable hair (pili trianguli et canaliculi): evidence for dominant inheritance with complete penetrance based on scanning electron microscopyA A Hebert, J Charrow, N B Esterly, et al.
American Journal of Human Genetics|July 1, 1983
Partial trisomy 14 (q23 leads to qter) via segregation of a 14/X translocationM M Cohen, J Charrow, N E Balkin, et al.
Medical and Pediatric Oncology|January 1, 1993
Carboplatin-induced regression of an optic pathway tumor in a child with neurofibromatosisJ Charrow, R Listernick, M J Greenwald, et al.
Neurology|November 24, 2004
Late-onset optic pathway tumors in children with neurofibromatosis 1R Listernick, R E Ferner, L Piersall, et al.
American Journal of Human Genetics|January 1, 1982
Apparently normal extracellular acidic alpha-mannosidase in fibroblast cultures from patients with mannosidosisY Ben-Yoseph, C L DeFranco, J Charrow, et al.
American Journal of Medical Genetics|April 11, 2000
Neural tube defects and the 13q deletion syndrome: evidence for a critical region in 13q33-34J Luo, N Balkin, J F Stewart, et al.
American Journal of Medical Genetics|March 3, 1998
Myelomeningocele and Waardenburg syndrome (type 3) in patients with interstitial deletions of 2q35 and the PAX3 gene: possible digenic inheritance of a neural tube defectJ S Nye, N Balkin, H Lucas, et al.
American Journal of Therapeutics|December 23, 2009
Psoriasis induced by losartan therapy: a case report and review of the literatureGurpreet Lamba, Chandrasekar Palaniswamy, Tarunjit Singh, et al.
The Journal of Pediatrics|July 1, 1996
Acceleration of retarded growth in children with Gaucher disease after treatment with algluceraseP Kaplan, A Mazur, O Manor, et al.
Teratology|February 8, 2000
Myelocystocele-cloacal exstrophy in a pedigree with a mitochondrial 12S rRNA mutation, aminoglycoside-induced deafness, pigmentary disturbances, and spinal anomaliesJ S Nye, E A Hayes, M Amendola, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics|September 1, 1987
Uncombable hair (pili trianguli et canaliculi): evidence for dominant inheritance with complete penetrance based on scanning electron microscopyA A Hebert, J Charrow, N B Esterly, et al.
American Journal of Human Genetics|July 1, 1983
Partial trisomy 14 (q23 leads to qter) via segregation of a 14/X translocationM M Cohen, J Charrow, N E Balkin, et al.
Medical and Pediatric Oncology|January 1, 1993
Carboplatin-induced regression of an optic pathway tumor in a child with neurofibromatosisJ Charrow, R Listernick, M J Greenwald, et al.
Neurology|November 24, 2004
Late-onset optic pathway tumors in children with neurofibromatosis 1R Listernick, R E Ferner, L Piersall, et al.
American Journal of Human Genetics|January 1, 1982
Apparently normal extracellular acidic alpha-mannosidase in fibroblast cultures from patients with mannosidosisY Ben-Yoseph, C L DeFranco, J Charrow, et al.
American Journal of Medical Genetics|April 11, 2000
Neural tube defects and the 13q deletion syndrome: evidence for a critical region in 13q33-34J Luo, N Balkin, J F Stewart, et al.
American Journal of Medical Genetics|March 3, 1998
Myelomeningocele and Waardenburg syndrome (type 3) in patients with interstitial deletions of 2q35 and the PAX3 gene: possible digenic inheritance of a neural tube defectJ S Nye, N Balkin, H Lucas, et al.
American Journal of Therapeutics|December 23, 2009
Psoriasis induced by losartan therapy: a case report and review of the literatureGurpreet Lamba, Chandrasekar Palaniswamy, Tarunjit Singh, et al.
The Journal of Pediatrics|July 1, 1996
Acceleration of retarded growth in children with Gaucher disease after treatment with algluceraseP Kaplan, A Mazur, O Manor, et al.
Teratology|February 8, 2000
Myelocystocele-cloacal exstrophy in a pedigree with a mitochondrial 12S rRNA mutation, aminoglycoside-induced deafness, pigmentary disturbances, and spinal anomaliesJ S Nye, E A Hayes, M Amendola, et al.
Pageof 5