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The Journal of Biological Chemistry
|
February 10, 1985
Altered triple helical structure of type I procollagen in lethal perinatal osteogenesis imperfecta
J Bonadio, K A Holbrook, R E Gelinas, et al.
Anatomy and Embryology
|
January 1, 1989
The appearance, density and distribution of melanocytes in human embryonic and fetal skin revealed by the anti-melanoma monoclonal antibody, HMB-45
K A Holbrook, R A Underwood, A M Vogel, et al.
The Journal of Investigative Dermatology
|
April 1, 1992
CHILD syndrome: lack of expression of epidermal differentiation markers in lesional ichthyotic skin
B A Dale, J R Kimball, P Fleckman, et al.
Experimental Cell Research
|
December 1, 1985
Age-related changes in collagenase expression in cultured embryonic and fetal human skin fibroblasts
E A Bauer, A Kronberger, G P Stricklin, et al.
JAMA
|
August 27, 1999
Users' guides to the medical literature: XIX. Applying clinical trial results. A. How to use an article measuring the effect of an intervention on surrogate end points. Evidence-Based Medicine Working Group
H C Bucher, G H Guyatt, D J Cook, et al.
Prenatal Diagnosis
|
January 1, 1986
Biochemical examination of fetal skin biopsy specimens obtained by fetoscopy: use of the method for analysis of keratins and filaggrin
B A Dale, T B Perry, K A Holbrook, et al.
Surgery
|
May 1, 1981
The treatment of innominate artery stenosis by intraoperative transluminal angioplasty
B G Lowman, L A Queral, W A Holbrook, et al.
Laboratory Medicine
|
October 15, 2022
A Novel INS Mutation in the C-Peptide Region Causing Hyperproinsulinemic Maturity Onset Diabetes of Youth Type 10
Amnon Schlegel, Whitney C Petersen, Alexandra A Holbrook, et al.
Birth Defects Original Article Series
|
January 1, 1978
Electron microscopy as an aid to diagnosis of disorders of the extracellular matrix: a new type of spondyloepiphyseal dysplasia
P H Byers, K A Holbrook, J W Chandler, et al.
Molecular Genetics and Metabolism
|
February 26, 2022
Lessons on the value of long term follow-up from genetic counselling of a family with severe autosomal recessive congenital ichthyosis
Janine El Helou, Tracy B Perry, Natascia Anastasio, et al.
Page
of 25
Search research articles
Search
Showing results (161-170 of 249) with videos related to
Sort By:
Page
of 25
The Journal of Biological Chemistry
|
February 10, 1985
Altered triple helical structure of type I procollagen in lethal perinatal osteogenesis imperfecta
J Bonadio, K A Holbrook, R E Gelinas, et al.
Anatomy and Embryology
|
January 1, 1989
The appearance, density and distribution of melanocytes in human embryonic and fetal skin revealed by the anti-melanoma monoclonal antibody, HMB-45
K A Holbrook, R A Underwood, A M Vogel, et al.
The Journal of Investigative Dermatology
|
April 1, 1992
CHILD syndrome: lack of expression of epidermal differentiation markers in lesional ichthyotic skin
B A Dale, J R Kimball, P Fleckman, et al.
Experimental Cell Research
|
December 1, 1985
Age-related changes in collagenase expression in cultured embryonic and fetal human skin fibroblasts
E A Bauer, A Kronberger, G P Stricklin, et al.
JAMA
|
August 27, 1999
Users' guides to the medical literature: XIX. Applying clinical trial results. A. How to use an article measuring the effect of an intervention on surrogate end points. Evidence-Based Medicine Working Group
H C Bucher, G H Guyatt, D J Cook, et al.
Prenatal Diagnosis
|
January 1, 1986
Biochemical examination of fetal skin biopsy specimens obtained by fetoscopy: use of the method for analysis of keratins and filaggrin
B A Dale, T B Perry, K A Holbrook, et al.
Surgery
|
May 1, 1981
The treatment of innominate artery stenosis by intraoperative transluminal angioplasty
B G Lowman, L A Queral, W A Holbrook, et al.
Laboratory Medicine
|
October 15, 2022
A Novel INS Mutation in the C-Peptide Region Causing Hyperproinsulinemic Maturity Onset Diabetes of Youth Type 10
Amnon Schlegel, Whitney C Petersen, Alexandra A Holbrook, et al.
Birth Defects Original Article Series
|
January 1, 1978
Electron microscopy as an aid to diagnosis of disorders of the extracellular matrix: a new type of spondyloepiphyseal dysplasia
P H Byers, K A Holbrook, J W Chandler, et al.
Molecular Genetics and Metabolism
|
February 26, 2022
Lessons on the value of long term follow-up from genetic counselling of a family with severe autosomal recessive congenital ichthyosis
Janine El Helou, Tracy B Perry, Natascia Anastasio, et al.
Page
of 25