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A Rappold

Showing results (111-120 of 160) with videos related to

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Pharmacogenetics|February 24, 2001
Serotonin receptor gene HTR3A variants in schizophrenic and bipolar affective patientsB Niesler, B Weiss, C Fischer, et al.
Genomics|May 1, 1992
Physical mapping of 14 new DNA markers isolated from the human distal Xp regionM C Wapenaar, C Petit, E Basler, et al.
European Journal of Human Genetics : EJHG|May 1, 2018
Functional missense and splicing variants in the retinoic acid catabolizing enzyme CYP26C1 in idiopathic short statureAntonino Montalbano, Lonny Juergensen, Maki Fukami, et al.
Journal of Medical Genetics|October 3, 1999
Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X maleL Stuppia, G Calabrese, P Borrelli, et al.
Frontiers in Endocrinology|December 28, 2023
Identification of novel genes including <i>NAV2</i> associated with isolated tall statureBirgit Weiss, Tim Ott, Philipp Vick, et al.
EMBO Molecular Medicine|November 19, 2016
Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiencyAntonino Montalbano, Lonny Juergensen, Ralph Roeth, et al.
Plos One|June 3, 2014
Identification of novel SHOX target genes in the developing limb using a transgenic mouse modelKatja U Beiser, Anne Glaser, Kerstin Kleinschmidt, et al.
Clinical Genetics|July 25, 2000
Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri-Weill dyschondrosteosisG Palka, L Stuppia, P Guanciali Franchi, et al.
Hormone Research in Paediatrics|May 14, 2015
Radiological Features in Patients with Short Stature Homeobox-Containing (SHOX) Gene Deficiency and Turner Syndrome before and after 2 Years of GH TreatmentChristopher J Child, Gabriel Kalifa, Christine Jones, et al.
Cell|April 7, 1995
A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathyB Franco, G Meroni, G Parenti, et al.
Pageof 16

Showing results (111-120 of 160) with videos related to

Sort By:
Pageof 16
Pharmacogenetics|February 24, 2001
Serotonin receptor gene HTR3A variants in schizophrenic and bipolar affective patientsB Niesler, B Weiss, C Fischer, et al.
Genomics|May 1, 1992
Physical mapping of 14 new DNA markers isolated from the human distal Xp regionM C Wapenaar, C Petit, E Basler, et al.
European Journal of Human Genetics : EJHG|May 1, 2018
Functional missense and splicing variants in the retinoic acid catabolizing enzyme CYP26C1 in idiopathic short statureAntonino Montalbano, Lonny Juergensen, Maki Fukami, et al.
Journal of Medical Genetics|October 3, 1999
Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X maleL Stuppia, G Calabrese, P Borrelli, et al.
Frontiers in Endocrinology|December 28, 2023
Identification of novel genes including <i>NAV2</i> associated with isolated tall statureBirgit Weiss, Tim Ott, Philipp Vick, et al.
EMBO Molecular Medicine|November 19, 2016
Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiencyAntonino Montalbano, Lonny Juergensen, Ralph Roeth, et al.
Plos One|June 3, 2014
Identification of novel SHOX target genes in the developing limb using a transgenic mouse modelKatja U Beiser, Anne Glaser, Kerstin Kleinschmidt, et al.
Clinical Genetics|July 25, 2000
Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri-Weill dyschondrosteosisG Palka, L Stuppia, P Guanciali Franchi, et al.
Hormone Research in Paediatrics|May 14, 2015
Radiological Features in Patients with Short Stature Homeobox-Containing (SHOX) Gene Deficiency and Turner Syndrome before and after 2 Years of GH TreatmentChristopher J Child, Gabriel Kalifa, Christine Jones, et al.
Cell|April 7, 1995
A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathyB Franco, G Meroni, G Parenti, et al.
Pageof 16