A Novel Deletion in the GH1 Gene Including the IVS3 Branch Site Responsible for Autosomal Dominant Isolated Growth Hormone Defic
![3D interactions with the growth hormone locus in cellular signalling and cancer-related pathways in: Journal of Molecular Endocrinology Volume 64 Issue 4 (2020) 3D interactions with the growth hormone locus in cellular signalling and cancer-related pathways in: Journal of Molecular Endocrinology Volume 64 Issue 4 (2020)](https://jme.bioscientifica.com/view/journals/jme/64/4/images/JME-20-0010fig1.jpeg)
3D interactions with the growth hormone locus in cellular signalling and cancer-related pathways in: Journal of Molecular Endocrinology Volume 64 Issue 4 (2020)
![Decreased Activity of the Ghrhr and Gh Promoters Causes Dominantly Inherited GH Deficiency | bioRxiv Decreased Activity of the Ghrhr and Gh Promoters Causes Dominantly Inherited GH Deficiency | bioRxiv](https://www.biorxiv.org/content/biorxiv/early/2019/02/08/545384/F1.large.jpg)
Decreased Activity of the Ghrhr and Gh Promoters Causes Dominantly Inherited GH Deficiency | bioRxiv
![Targeting growth hormone function: strategies and therapeutic applications | Signal Transduction and Targeted Therapy Targeting growth hormone function: strategies and therapeutic applications | Signal Transduction and Targeted Therapy](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41392-019-0036-y/MediaObjects/41392_2019_36_Fig4_HTML.png)
Targeting growth hormone function: strategies and therapeutic applications | Signal Transduction and Targeted Therapy
![Prevalence of Human GH-1 Gene Alterations in Patients with Isolated Growth Hormone Deficiency | Pediatric Research Prevalence of Human GH-1 Gene Alterations in Patients with Isolated Growth Hormone Deficiency | Pediatric Research](https://media.springernature.com/m685/springer-static/image/art%3A10.1203%2F00006450-199801000-00016/MediaObjects/41390_1998_Article_BFpr199816_Fig1_HTML.jpg)
Prevalence of Human GH-1 Gene Alterations in Patients with Isolated Growth Hormone Deficiency | Pediatric Research
![Genetic causes and treatment of isolated growth hormone deficiency—an update | Nature Reviews Endocrinology Genetic causes and treatment of isolated growth hormone deficiency—an update | Nature Reviews Endocrinology](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fnrendo.2010.147/MediaObjects/41574_2010_Article_BFnrendo2010147_Fig1_HTML.jpg)
Genetic causes and treatment of isolated growth hormone deficiency—an update | Nature Reviews Endocrinology
![Figure 2 from Type IA isolated growth hormone deficiency (IGHD) consistent with compound heterozygous deletions of 6.7 and 7.6 Kb at the GH1 gene locus. | Semantic Scholar Figure 2 from Type IA isolated growth hormone deficiency (IGHD) consistent with compound heterozygous deletions of 6.7 and 7.6 Kb at the GH1 gene locus. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/9231774e8860aa4e52039e6d60da3bd6c0f5b401/2-Table1-1.png)
Figure 2 from Type IA isolated growth hormone deficiency (IGHD) consistent with compound heterozygous deletions of 6.7 and 7.6 Kb at the GH1 gene locus. | Semantic Scholar
![Frontiers | A GHRHR founder mutation causes isolated growth hormone deficiency type IV in a consanguineous Pakistani family Frontiers | A GHRHR founder mutation causes isolated growth hormone deficiency type IV in a consanguineous Pakistani family](https://www.frontiersin.org/files/Articles/1066182/fendo-14-1066182-HTML-r1/image_m/fendo-14-1066182-g001.jpg)
Frontiers | A GHRHR founder mutation causes isolated growth hormone deficiency type IV in a consanguineous Pakistani family
![Figure 2 from Type IA isolated growth hormone deficiency (IGHD) consistent with compound heterozygous deletions of 6.7 and 7.6 Kb at the GH1 gene locus. | Semantic Scholar Figure 2 from Type IA isolated growth hormone deficiency (IGHD) consistent with compound heterozygous deletions of 6.7 and 7.6 Kb at the GH1 gene locus. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/9231774e8860aa4e52039e6d60da3bd6c0f5b401/4-Figure2-1.png)
Figure 2 from Type IA isolated growth hormone deficiency (IGHD) consistent with compound heterozygous deletions of 6.7 and 7.6 Kb at the GH1 gene locus. | Semantic Scholar
![Location and pairwise LD values of the SNPs in the GH1 gene and the... | Download Scientific Diagram Location and pairwise LD values of the SNPs in the GH1 gene and the... | Download Scientific Diagram](https://www.researchgate.net/publication/5689899/figure/fig2/AS:667608638562305@1536181711017/Location-and-pairwise-LD-values-of-the-SNPs-in-the-GH1-gene-and-the-145-kb-upstream-LCR.png)