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American Journal of Medical Genetics
|
March 1, 1989
Acrocallosal syndrome: new findings
J 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 tangles
J A Golden, G P Nielsen, B R Pober, et al.
Human Pathology
|
December 1, 1986
Isolated congenital renal tubular immaturity in siblings
B 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 utero
C 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 syndrome
B 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 sisters
F M Hisama, S Zemel, E M Cherniske, et al.
Clinical Dysmorphology
|
May 13, 1999
Early puberty in Williams syndrome
E 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 phenotypes
S Y Li, L H Gibson, K Gomez, et al.
The Journal of Pediatrics
|
December 18, 2001
Differences by sex in cardiovascular disease in Williams syndrome
L 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 infection
D R Snydman, H F Gorbea, B R Pober, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 32) with videos related to
Sort By:
Page
of 4
American Journal of Medical Genetics
|
March 1, 1989
Acrocallosal syndrome: new findings
J 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 tangles
J A Golden, G P Nielsen, B R Pober, et al.
Human Pathology
|
December 1, 1986
Isolated congenital renal tubular immaturity in siblings
B 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 utero
C 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 syndrome
B 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 sisters
F M Hisama, S Zemel, E M Cherniske, et al.
Clinical Dysmorphology
|
May 13, 1999
Early puberty in Williams syndrome
E 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 phenotypes
S Y Li, L H Gibson, K Gomez, et al.
The Journal of Pediatrics
|
December 18, 2001
Differences by sex in cardiovascular disease in Williams syndrome
L 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 infection
D R Snydman, H F Gorbea, B R Pober, et al.
Page
of 4