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 (11-20 of 40) with videos related to

Pageof 4
Sort By:
American Journal of Medical Genetics|June 1, 1984
Forearm fullness in Coffin-Lowry syndrome: a misleading yet possible early diagnostic clueJ H Hersh, B Weisskopf, C DeCoster
Journal of Developmental and Behavioral Pediatrics : JDBP|December 1, 1982
Childhood Autism in a female with Coffin Siris SyndromeJ H Hersh, A S Bloom, B Weisskopf
Archives of Internal Medicine|September 1, 1971
Chromosome aberrations in the child of a kidney transplant recipientD E Leb, B Weisskopf, B S Kanovitz
Journal of Medical Genetics|February 1, 1989
A terminal deletion (14)(q31.1) in a child with microcephaly, narrow palate, gingival hypertrophy, protuberant ears, and mild mental retardationF S Yen, P E Podruch, B Weisskopf
Birth Defects Original Article Series|January 1, 1982
Pigmentary retinopathy, hearing loss, mental retardation, and dysmorphism in sibs: a new syndrome?J H Hersh, P E Podruch, B Weisskopf
Pediatric Radiology|February 1, 1980
An unusual case of short limbed dwarfism and thoracic dystrophy with normal spine, hands and feetN D Dinno, L T Shearer, B Weisskopf
Clinical Genetics|January 1, 1974
47, XY, t(9pplus;11qplus) in a mlae infant with multiple malformationsN D Dinno, G L Silvey, B Weisskopf
Archives of Disease in Childhood|February 1, 1972
Syndrome of growth resistance, obesity, and intellectual impairment with precocious pubertyD R Macmillan, C B Kim, B Weisskopf
The Journal of Pediatrics|August 1, 1981
Pseudo-Menke syndromeN D Dinno, U Yacoub, W Holmes, et al.
Journal of Pediatric Ophthalmology and Strabismus|January 1, 1987
Familial iridoplegiaJ H Hersh, C Douglas, J Houston, et al.
Pageof 4

Showing results (11-20 of 40) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics|June 1, 1984
Forearm fullness in Coffin-Lowry syndrome: a misleading yet possible early diagnostic clueJ H Hersh, B Weisskopf, C DeCoster
Journal of Developmental and Behavioral Pediatrics : JDBP|December 1, 1982
Childhood Autism in a female with Coffin Siris SyndromeJ H Hersh, A S Bloom, B Weisskopf
Archives of Internal Medicine|September 1, 1971
Chromosome aberrations in the child of a kidney transplant recipientD E Leb, B Weisskopf, B S Kanovitz
Journal of Medical Genetics|February 1, 1989
A terminal deletion (14)(q31.1) in a child with microcephaly, narrow palate, gingival hypertrophy, protuberant ears, and mild mental retardationF S Yen, P E Podruch, B Weisskopf
Birth Defects Original Article Series|January 1, 1982
Pigmentary retinopathy, hearing loss, mental retardation, and dysmorphism in sibs: a new syndrome?J H Hersh, P E Podruch, B Weisskopf
Pediatric Radiology|February 1, 1980
An unusual case of short limbed dwarfism and thoracic dystrophy with normal spine, hands and feetN D Dinno, L T Shearer, B Weisskopf
Clinical Genetics|January 1, 1974
47, XY, t(9pplus;11qplus) in a mlae infant with multiple malformationsN D Dinno, G L Silvey, B Weisskopf
Archives of Disease in Childhood|February 1, 1972
Syndrome of growth resistance, obesity, and intellectual impairment with precocious pubertyD R Macmillan, C B Kim, B Weisskopf
The Journal of Pediatrics|August 1, 1981
Pseudo-Menke syndromeN D Dinno, U Yacoub, W Holmes, et al.
Journal of Pediatric Ophthalmology and Strabismus|January 1, 1987
Familial iridoplegiaJ H Hersh, C Douglas, J Houston, et al.
Pageof 4