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B R Pober

Showing results (11-20 of 32) with videos related to

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American Journal of Medical Genetics|March 1, 1989
Acrocallosal syndrome: new findingsJ B Moeschler, B R Pober, L B Holmes, et al.
Archives of Neurology|February 1, 1995
The neuropathology of Williams syndrome. Report of a 35-year-old man with presenile beta/A4 amyloid plaques and neurofibrillary tanglesJ A Golden, G P Nielsen, B R Pober, et al.
Human Pathology|December 1, 1986
Isolated congenital renal tubular immaturity in siblingsB R Schwartz, J M Lage, B R Pober, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|March 1, 1988
Sonography of Nager acrofacial dysostosis syndrome in uteroC B Benson, B R Pober, M P Hirsh, et al.
American Journal of Medical Genetics|May 15, 1993
Renal findings in 40 individuals with Williams syndromeB R Pober, R V Lacro, C Rice, et al.
American Journal of Medical Genetics|February 27, 2001
46,XX gonadal dysgenesis, short stature, and recurrent metabolic acidosis in two sistersF M Hisama, S Zemel, E M Cherniske, et al.
Clinical Dysmorphology|May 13, 1999
Early puberty in Williams syndromeE M Cherniske, L S Sadler, D Schwartz, et al.
American Journal of Medical Genetics|February 5, 1998
Familial dup(5)(q15q21) associated with normal and abnormal phenotypesS Y Li, L H Gibson, K Gomez, et al.
The Journal of Pediatrics|December 18, 2001
Differences by sex in cardiovascular disease in Williams syndromeL S Sadler, B R Pober, A Grandinetti, et al.
Lancet (London, England)|December 18, 1982
Predictive value of surveillance skin cultures in total-parenteral-nutrition-related infectionD R Snydman, H F Gorbea, B R Pober, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics|March 1, 1989
Acrocallosal syndrome: new findingsJ B Moeschler, B R Pober, L B Holmes, et al.
Archives of Neurology|February 1, 1995
The neuropathology of Williams syndrome. Report of a 35-year-old man with presenile beta/A4 amyloid plaques and neurofibrillary tanglesJ A Golden, G P Nielsen, B R Pober, et al.
Human Pathology|December 1, 1986
Isolated congenital renal tubular immaturity in siblingsB R Schwartz, J M Lage, B R Pober, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|March 1, 1988
Sonography of Nager acrofacial dysostosis syndrome in uteroC B Benson, B R Pober, M P Hirsh, et al.
American Journal of Medical Genetics|May 15, 1993
Renal findings in 40 individuals with Williams syndromeB R Pober, R V Lacro, C Rice, et al.
American Journal of Medical Genetics|February 27, 2001
46,XX gonadal dysgenesis, short stature, and recurrent metabolic acidosis in two sistersF M Hisama, S Zemel, E M Cherniske, et al.
Clinical Dysmorphology|May 13, 1999
Early puberty in Williams syndromeE M Cherniske, L S Sadler, D Schwartz, et al.
American Journal of Medical Genetics|February 5, 1998
Familial dup(5)(q15q21) associated with normal and abnormal phenotypesS Y Li, L H Gibson, K Gomez, et al.
The Journal of Pediatrics|December 18, 2001
Differences by sex in cardiovascular disease in Williams syndromeL S Sadler, B R Pober, A Grandinetti, et al.
Lancet (London, England)|December 18, 1982
Predictive value of surveillance skin cultures in total-parenteral-nutrition-related infectionD R Snydman, H F Gorbea, B R Pober, et al.
Pageof 4