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

B Weisskopf

Showing results (21-30 of 40) with videos related to

Pageof 4
Sort By:
Clinical Genetics|August 18, 1999
Vaginal uterine agenesis associated with amastia in a phenotypic female with a de novo 46,XX,t(8;13)(q22.1;q32.1) translocationL Amesse, F F Yen, B Weisskopf, et al.
The Journal of Pediatrics|June 1, 1985
Toluene embryopathyJ H Hersh, P E Podruch, G Rogers, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|January 1, 1988
Methylphenidate-induced delusional disorder in a child with attention deficit disorder with hyperactivityA S Bloom, L J Russell, B Weisskopf, et al.
JAMA|August 16, 1985
Retinoic acid embryopathy: timing of exposure and effects on fetal developmentJ H Hersh, D E Danhauer, M E Hand, et al.
Cutis|August 1, 1977
Macrodactyly and epidermal nevusN D Dinno, L G Owen, B Weisskopf, et al.
Southern Medical Journal|October 1, 1989
Ivemark's "asplenia" syndrome: a single gene disorderR H McChane, J H Hersh, L J Russell, et al.
Journal of Medical Genetics|October 1, 1982
Yq- in a child with livedo reticularis, snub nose, microcephaly, and profound mental retardationP E Podruch, F S Yen, N D Dinno, et al.
Birth Defects Original Article Series|January 1, 1976
Bilateral microcornea, coloboma, short stature and other skeletal anomalies - a new hereditary syndromeN D Dinno, T Lawwill, A E Leggett, et al.
Clinical Pediatrics|February 1, 1986
Townes syndrome. A distinct multiple malformation syndrome resembling VACTERL associationJ H Hersh, M Jaworski, R E Solinger, et al.
Research in Developmental Disabilities|January 1, 1988
Mild intellectual deficits in a child with 49,XXXXYJ H Hersh, A S Bloom, F Yen, et al.
Pageof 4

Showing results (21-30 of 40) with videos related to

Sort By:
Pageof 4
Clinical Genetics|August 18, 1999
Vaginal uterine agenesis associated with amastia in a phenotypic female with a de novo 46,XX,t(8;13)(q22.1;q32.1) translocationL Amesse, F F Yen, B Weisskopf, et al.
The Journal of Pediatrics|June 1, 1985
Toluene embryopathyJ H Hersh, P E Podruch, G Rogers, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|January 1, 1988
Methylphenidate-induced delusional disorder in a child with attention deficit disorder with hyperactivityA S Bloom, L J Russell, B Weisskopf, et al.
JAMA|August 16, 1985
Retinoic acid embryopathy: timing of exposure and effects on fetal developmentJ H Hersh, D E Danhauer, M E Hand, et al.
Cutis|August 1, 1977
Macrodactyly and epidermal nevusN D Dinno, L G Owen, B Weisskopf, et al.
Southern Medical Journal|October 1, 1989
Ivemark's "asplenia" syndrome: a single gene disorderR H McChane, J H Hersh, L J Russell, et al.
Journal of Medical Genetics|October 1, 1982
Yq- in a child with livedo reticularis, snub nose, microcephaly, and profound mental retardationP E Podruch, F S Yen, N D Dinno, et al.
Birth Defects Original Article Series|January 1, 1976
Bilateral microcornea, coloboma, short stature and other skeletal anomalies - a new hereditary syndromeN D Dinno, T Lawwill, A E Leggett, et al.
Clinical Pediatrics|February 1, 1986
Townes syndrome. A distinct multiple malformation syndrome resembling VACTERL associationJ H Hersh, M Jaworski, R E Solinger, et al.
Research in Developmental Disabilities|January 1, 1988
Mild intellectual deficits in a child with 49,XXXXYJ H Hersh, A S Bloom, F Yen, et al.
Pageof 4