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G Grigelioniene

Showing results (1-10 of 12) with videos related to

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Acta Radiologica (Stockholm, Sweden : 1987)|May 21, 2005
Metacarpophalangeal pattern profile analysis in Leri-Weill dyschondrosteosisE Laurencikas, E Soderman, G Grigelioniene, et al.
The Journal of Steroid Biochemistry and Molecular Biology|February 13, 2001
Estrogens and human growthE M Ritzén, O Nilsson, G Grigelioniene, et al.
Bone|March 10, 2016
Decreased fracture rate, pharmacogenetics and BMD response in 79 Swedish children with osteogenesis imperfecta types I, III and IV treated with PamidronateK Lindahl, A Kindmark, C-J Rubin, et al.
Oral Diseases|August 12, 2016
Tooth agenesis in osteogenesis imperfecta related to mutations in the collagen type I genesB Malmgren, K Andersson, K Lindahl, et al.
Clinical Genetics|March 7, 2014
SLC26A2 disease spectrum in Sweden - high frequency of recessive multiple epiphyseal dysplasia (rMED)O Mäkitie, S Geiberger, E Horemuzova, et al.
The Journal of Clinical Endocrinology and Metabolism|January 27, 1999
Demonstration of estrogen receptor-beta immunoreactivity in human growth plate cartilageL O Nilsson, A Boman, L Sävendahl, et al.
Human Genetics|October 13, 2000
Mutations in short stature homeobox containing gene (SHOX) in dyschondrosteosis but not in hypochondroplasiaG Grigelioniene, O Eklöf, S A Ivarsson, et al.
Clinical Genetics|July 26, 2014
Autosomal recessive mutations in the COL2A1 gene cause severe spondyloepiphyseal dysplasiaE Tham, G Nishimura, S Geiberger, et al.
Hormone Research in Paediatrics|April 3, 2015
Short Stature in KBG Syndrome: First Responses to Growth Hormone TreatmentNele Reynaert, C W Ockeloen, L Sävendahl, et al.
Human Genetics|December 6, 2001
Analysis of short stature homeobox-containing gene ( SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformityG Grigelioniene, J Schoumans, L Neumeyer, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Acta Radiologica (Stockholm, Sweden : 1987)|May 21, 2005
Metacarpophalangeal pattern profile analysis in Leri-Weill dyschondrosteosisE Laurencikas, E Soderman, G Grigelioniene, et al.
The Journal of Steroid Biochemistry and Molecular Biology|February 13, 2001
Estrogens and human growthE M Ritzén, O Nilsson, G Grigelioniene, et al.
Bone|March 10, 2016
Decreased fracture rate, pharmacogenetics and BMD response in 79 Swedish children with osteogenesis imperfecta types I, III and IV treated with PamidronateK Lindahl, A Kindmark, C-J Rubin, et al.
Oral Diseases|August 12, 2016
Tooth agenesis in osteogenesis imperfecta related to mutations in the collagen type I genesB Malmgren, K Andersson, K Lindahl, et al.
Clinical Genetics|March 7, 2014
SLC26A2 disease spectrum in Sweden - high frequency of recessive multiple epiphyseal dysplasia (rMED)O Mäkitie, S Geiberger, E Horemuzova, et al.
The Journal of Clinical Endocrinology and Metabolism|January 27, 1999
Demonstration of estrogen receptor-beta immunoreactivity in human growth plate cartilageL O Nilsson, A Boman, L Sävendahl, et al.
Human Genetics|October 13, 2000
Mutations in short stature homeobox containing gene (SHOX) in dyschondrosteosis but not in hypochondroplasiaG Grigelioniene, O Eklöf, S A Ivarsson, et al.
Clinical Genetics|July 26, 2014
Autosomal recessive mutations in the COL2A1 gene cause severe spondyloepiphyseal dysplasiaE Tham, G Nishimura, S Geiberger, et al.
Hormone Research in Paediatrics|April 3, 2015
Short Stature in KBG Syndrome: First Responses to Growth Hormone TreatmentNele Reynaert, C W Ockeloen, L Sävendahl, et al.
Human Genetics|December 6, 2001
Analysis of short stature homeobox-containing gene ( SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformityG Grigelioniene, J Schoumans, L Neumeyer, et al.
Pageof 2