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Reproductive Biology
|
August 5, 2008
Decreased expression of pigment epithelium derived factor (PEDF), an inhibitor of angiogenesis, in placentas of unexplained stillbirths
Beth A Plunkett, Philip Fitchev, Jennifer A Doll, et al.
Current Biology : CB
|
August 1, 1995
Patterning activities of vertebrate hedgehog proteins in the developing eye and brain
S C Ekker, A R Ungar, P Greenstein, et al.
Journal of the Academy of Consultation-Liaison Psychiatry
|
December 15, 2022
A 10-Year Follow-up Survey of Psychiatry Resident Education in Consultation-Liaison Psychiatry
Scott R Beach, Carrie L Ernst, Mallika Lavakumar, et al.
Journal of the Academy of Consultation-Liaison Psychiatry
|
November 12, 2024
2024 ACLP Recommendations for Training Residents in Consultation-Liaison Psychiatry
Scott R Beach, Carrie L Ernst, David C Fipps, et al.
Neurology
|
September 12, 2000
Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA
C L Karadimas, P Greenstein, C M Sue, et al.
Page
of 7
Search research articles
Search
Showing results (61-70 of 65) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 65 results.
Reproductive Biology
|
August 5, 2008
Decreased expression of pigment epithelium derived factor (PEDF), an inhibitor of angiogenesis, in placentas of unexplained stillbirths
Beth A Plunkett, Philip Fitchev, Jennifer A Doll, et al.
Current Biology : CB
|
August 1, 1995
Patterning activities of vertebrate hedgehog proteins in the developing eye and brain
S C Ekker, A R Ungar, P Greenstein, et al.
Journal of the Academy of Consultation-Liaison Psychiatry
|
December 15, 2022
A 10-Year Follow-up Survey of Psychiatry Resident Education in Consultation-Liaison Psychiatry
Scott R Beach, Carrie L Ernst, Mallika Lavakumar, et al.
Journal of the Academy of Consultation-Liaison Psychiatry
|
November 12, 2024
2024 ACLP Recommendations for Training Residents in Consultation-Liaison Psychiatry
Scott R Beach, Carrie L Ernst, David C Fipps, et al.
Neurology
|
September 12, 2000
Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA
C L Karadimas, P Greenstein, C M Sue, et al.
Page
of 7