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Annals of Burns and Fire Disasters
|
January 1, 2025
Burn hypertrophy scarring assessment based on patient and observer scar assessment scale (POSAS)
M H Oley, M C Oley, F L F G Langi, et al.
American Journal of Medical Genetics
|
April 15, 1994
Nevoid basal cell carcinoma syndrome: review of 118 affected individuals
S Shanley, J Ratcliffe, A Hockey, et al.
American Journal of Human Genetics
|
September 1, 1993
Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: linkage and loss of heterozygosity
G Chenevix-Trench, C Wicking, J Berkman, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
October 17, 2007
Androgen receptor genotyping in a large Australasian cohort with androgen insensitivity syndrome; identification of four novel mutations
Y W A Jeske, I N McGown, D M Cowley, et al.
Neuromuscular Disorders : NMD
|
February 5, 2003
Principal mutation hotspot for central core disease and related myopathies in the C-terminal transmembrane region of the RYR1 gene
M R Davis, E Haan, H Jungbluth, et al.
American Journal of Human Genetics
|
June 18, 2005
Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome
D Beysen, J Raes, B P Leroy, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 16) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 16 results.
Annals of Burns and Fire Disasters
|
January 1, 2025
Burn hypertrophy scarring assessment based on patient and observer scar assessment scale (POSAS)
M H Oley, M C Oley, F L F G Langi, et al.
American Journal of Medical Genetics
|
April 15, 1994
Nevoid basal cell carcinoma syndrome: review of 118 affected individuals
S Shanley, J Ratcliffe, A Hockey, et al.
American Journal of Human Genetics
|
September 1, 1993
Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: linkage and loss of heterozygosity
G Chenevix-Trench, C Wicking, J Berkman, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
October 17, 2007
Androgen receptor genotyping in a large Australasian cohort with androgen insensitivity syndrome; identification of four novel mutations
Y W A Jeske, I N McGown, D M Cowley, et al.
Neuromuscular Disorders : NMD
|
February 5, 2003
Principal mutation hotspot for central core disease and related myopathies in the C-terminal transmembrane region of the RYR1 gene
M R Davis, E Haan, H Jungbluth, et al.
American Journal of Human Genetics
|
June 18, 2005
Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome
D Beysen, J Raes, B P Leroy, et al.
Page
of 2