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European Journal of Human Genetics : EJHG
|
April 11, 2000
Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family
D P Kelsell, A L Wilgoss, G Richard, et al.
Oncology
|
January 1, 1984
Cases of carcinoma of thyroid following iodine-131 therapy for hyperthyroidism
A A Gossage, F E Neal, C M Ross, et al.
Journal of Medical Genetics
|
September 1, 1994
A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21
C S Munro, S Carter, S Bryce, et al.
Journal of the Royal College of Physicians of London
|
January 1, 1990
Clinical outcome and costs of care in radioiodine treatment of hyperthyroidism
C A Hardisty, S J Jones, A J Hedley, et al.
Magnetic Resonance in Medicine
|
September 26, 2024
Compressed sensing reconstruction for high-SNR, rapid dissolved <sup>129</sup>Xe gas exchange MRI
Jemima H Pilgrim-Morris, Guilhem J Collier, Ryan S Munro, et al.
The Journal of Investigative Dermatology
|
June 12, 2004
Hailey-Hailey disease: identification of novel mutations in ATP2C1 and effect of missense mutation A528P on protein expression levels
Rebecca J Fairclough, Lorne Lonie, Kurt Van Baelen, et al.
Ophthalmic Plastic and Reconstructive Surgery
|
June 1, 1995
The use of Vicryl mesh (polyglactin 910) for implantation of hydroxyapatite orbital implants
D R Jordan, L H Allen, A Ells, et al.
Scandinavian Journal of Immunology
|
May 1, 1987
Dendritic cells in cutaneous, lymph node and pulmonary lesions of sarcoidosis
C S Munro, D A Campbell, R M Du Bois, et al.
Thorax
|
June 1, 1988
Suppression associated lymphocyte markers in lesions of sarcoidosis
C S Munro, D A Campbell, R M Du Bois, et al.
The Journal of Endocrinology
|
September 1, 1988
Extracellular calmodulin and its association with epidermal growth factor in normal human body fluids
S MacNeil, R A Dawson, G Crocker, et al.
Page
of 34
Search research articles
Search
Showing results (251-260 of 335) with videos related to
Sort By:
Page
of 34
European Journal of Human Genetics : EJHG
|
April 11, 2000
Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family
D P Kelsell, A L Wilgoss, G Richard, et al.
Oncology
|
January 1, 1984
Cases of carcinoma of thyroid following iodine-131 therapy for hyperthyroidism
A A Gossage, F E Neal, C M Ross, et al.
Journal of Medical Genetics
|
September 1, 1994
A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21
C S Munro, S Carter, S Bryce, et al.
Journal of the Royal College of Physicians of London
|
January 1, 1990
Clinical outcome and costs of care in radioiodine treatment of hyperthyroidism
C A Hardisty, S J Jones, A J Hedley, et al.
Magnetic Resonance in Medicine
|
September 26, 2024
Compressed sensing reconstruction for high-SNR, rapid dissolved <sup>129</sup>Xe gas exchange MRI
Jemima H Pilgrim-Morris, Guilhem J Collier, Ryan S Munro, et al.
The Journal of Investigative Dermatology
|
June 12, 2004
Hailey-Hailey disease: identification of novel mutations in ATP2C1 and effect of missense mutation A528P on protein expression levels
Rebecca J Fairclough, Lorne Lonie, Kurt Van Baelen, et al.
Ophthalmic Plastic and Reconstructive Surgery
|
June 1, 1995
The use of Vicryl mesh (polyglactin 910) for implantation of hydroxyapatite orbital implants
D R Jordan, L H Allen, A Ells, et al.
Scandinavian Journal of Immunology
|
May 1, 1987
Dendritic cells in cutaneous, lymph node and pulmonary lesions of sarcoidosis
C S Munro, D A Campbell, R M Du Bois, et al.
Thorax
|
June 1, 1988
Suppression associated lymphocyte markers in lesions of sarcoidosis
C S Munro, D A Campbell, R M Du Bois, et al.
The Journal of Endocrinology
|
September 1, 1988
Extracellular calmodulin and its association with epidermal growth factor in normal human body fluids
S MacNeil, R A Dawson, G Crocker, et al.
Page
of 34