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Showing results (131-140 of 160) with videos related to

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Journal of Medical Genetics|October 4, 2002
Prevalence of mutations in the short stature homeobox containing gene (SHOX) in Madelung deformity of childhoodS F Flanagan, C F J Munns, M Hayes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
Identification of SLC20A1 and SLC15A4 among other genes as potential risk factors for combined pituitary hormone deficiencyFranziska Simm, Anne Griesbeck, Daniela Choukair, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 30, 2003
Familial growth and skeletal features associated with SHOX haploinsufficiencyC F J Munns, I A Glass, S Flanagan, et al.
Connective Tissue Research|May 25, 2007
Human mesenchymal stem cells derived from bone marrow display a better chondrogenic differentiation compared with other sourcesM E Bernardo, J A M Emons, M Karperien, et al.
Biochimica Et Biophysica Acta. Gene Regulatory Mechanisms|March 11, 2021
Network-driven discovery yields new insight into Shox2-dependent cardiac rhythm controlS Hoffmann, S Schmitteckert, K Raedecke, et al.
Developmental Genetics|December 8, 1998
Klinefelter's syndrome as a model of anomalous cerebral laterality: testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarrayD H Geschwind, J Gregg, K Boone, et al.
Molecular Psychiatry|May 22, 2021
Imbalanced post- and extrasynaptic SHANK2A functions during development affect social behavior in SHANK2-mediated neuropsychiatric disordersAhmed Eltokhi, Miguel A Gonzalez-Lozano, Lars-Lennart Oettl, et al.
Molecular Psychiatry|July 8, 2021
Correction: Imbalanced post- and extrasynaptic SHANK2A functions during development affect social behavior in SHANK2-mediated neuropsychiatric disordersAhmed Eltokhi, Miguel A Gonzalez-Lozano, Lars-Lennart Oettl, et al.
Hormone Research in Paediatrics|December 4, 2013
Alu-mediated recombination defect in IGF1R: haploinsufficiency in a patient with short statureEva-Maria Harmel, Gerhard Binder, Anja Barnikol-Oettler, et al.
Journal of the American Heart Association|January 22, 2026
<i>CAV1</i>-A Susceptibility Gene for Atrial Fibrillation: The Impact of Coding and Noncoding VariantsKristin Rädecke, David Rheinert, Annette Löwen, et al.
Pageof 16

Showing results (131-140 of 160) with videos related to

Sort By:
Pageof 16
Journal of Medical Genetics|October 4, 2002
Prevalence of mutations in the short stature homeobox containing gene (SHOX) in Madelung deformity of childhoodS F Flanagan, C F J Munns, M Hayes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
Identification of SLC20A1 and SLC15A4 among other genes as potential risk factors for combined pituitary hormone deficiencyFranziska Simm, Anne Griesbeck, Daniela Choukair, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 30, 2003
Familial growth and skeletal features associated with SHOX haploinsufficiencyC F J Munns, I A Glass, S Flanagan, et al.
Connective Tissue Research|May 25, 2007
Human mesenchymal stem cells derived from bone marrow display a better chondrogenic differentiation compared with other sourcesM E Bernardo, J A M Emons, M Karperien, et al.
Biochimica Et Biophysica Acta. Gene Regulatory Mechanisms|March 11, 2021
Network-driven discovery yields new insight into Shox2-dependent cardiac rhythm controlS Hoffmann, S Schmitteckert, K Raedecke, et al.
Developmental Genetics|December 8, 1998
Klinefelter's syndrome as a model of anomalous cerebral laterality: testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarrayD H Geschwind, J Gregg, K Boone, et al.
Molecular Psychiatry|May 22, 2021
Imbalanced post- and extrasynaptic SHANK2A functions during development affect social behavior in SHANK2-mediated neuropsychiatric disordersAhmed Eltokhi, Miguel A Gonzalez-Lozano, Lars-Lennart Oettl, et al.
Molecular Psychiatry|July 8, 2021
Correction: Imbalanced post- and extrasynaptic SHANK2A functions during development affect social behavior in SHANK2-mediated neuropsychiatric disordersAhmed Eltokhi, Miguel A Gonzalez-Lozano, Lars-Lennart Oettl, et al.
Hormone Research in Paediatrics|December 4, 2013
Alu-mediated recombination defect in IGF1R: haploinsufficiency in a patient with short statureEva-Maria Harmel, Gerhard Binder, Anja Barnikol-Oettler, et al.
Journal of the American Heart Association|January 22, 2026
<i>CAV1</i>-A Susceptibility Gene for Atrial Fibrillation: The Impact of Coding and Noncoding VariantsKristin Rädecke, David Rheinert, Annette Löwen, et al.
Pageof 16