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R Mühlenberg

Showing results (1-10 of 8) with videos related to

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Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|December 2, 2005
Mild congenital primary hypothyroidism in a Turkish family caused by a homozygous missense thyrotropin receptor (TSHR) gene mutation (A593 V)S Fricke-Otto, N Pfarr, R Mühlenberg, et al.
Klinische Padiatrie|March 1, 1991
Growth in children with adrenocortical tumorsB P Hauffa, C Roll, R Mühlenberg, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|October 1, 1981
[Priapism in childhood (author's transl)]H W Asbach, S Kösters, P Thomas, et al.
Hormone Research|February 16, 2002
A new C-terminal located mutation (V272ter) in the PIT-1 gene manifesting with severe congenital hypothyroidism. Possible functionality of the PIT-1 C-terminusO Blankenstein, R Mühlenberg, C Kim, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|March 21, 2013
Congenital goitrous primary hypothyroidism in two German families caused by novel thyroid peroxidase (TPO) gene mutationsK Altmann, P Hermanns, R Mühlenberg, et al.
Journal of Medical Genetics|September 19, 2009
Submicroscopic chromosomal imbalances in idiopathic Silver-Russell syndrome (SRS): the SRS phenotype overlaps with the 12q14 microdeletion syndromeS Spengler, N Schönherr, G Binder, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
Growth retardation in Turner syndrome: aneuploidy, rather than specific gene loss, may explain growth failureF Haverkamp, J Wölfle, K Zerres, et al.
Clinical Genetics|August 27, 2010
Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissuesM Begemann, S Spengler, D Kanber, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|December 2, 2005
Mild congenital primary hypothyroidism in a Turkish family caused by a homozygous missense thyrotropin receptor (TSHR) gene mutation (A593 V)S Fricke-Otto, N Pfarr, R Mühlenberg, et al.
Klinische Padiatrie|March 1, 1991
Growth in children with adrenocortical tumorsB P Hauffa, C Roll, R Mühlenberg, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|October 1, 1981
[Priapism in childhood (author's transl)]H W Asbach, S Kösters, P Thomas, et al.
Hormone Research|February 16, 2002
A new C-terminal located mutation (V272ter) in the PIT-1 gene manifesting with severe congenital hypothyroidism. Possible functionality of the PIT-1 C-terminusO Blankenstein, R Mühlenberg, C Kim, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|March 21, 2013
Congenital goitrous primary hypothyroidism in two German families caused by novel thyroid peroxidase (TPO) gene mutationsK Altmann, P Hermanns, R Mühlenberg, et al.
Journal of Medical Genetics|September 19, 2009
Submicroscopic chromosomal imbalances in idiopathic Silver-Russell syndrome (SRS): the SRS phenotype overlaps with the 12q14 microdeletion syndromeS Spengler, N Schönherr, G Binder, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
Growth retardation in Turner syndrome: aneuploidy, rather than specific gene loss, may explain growth failureF Haverkamp, J Wölfle, K Zerres, et al.
Clinical Genetics|August 27, 2010
Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissuesM Begemann, S Spengler, D Kanber, et al.
Pageof 1