![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
![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
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Schematic representation of the human GH1 gene showing the alternative... | Download Scientific Diagram
![GH1 gene structure and disease causing mutations. A, the GH1 gene is... | Download Scientific Diagram GH1 gene structure and disease causing mutations. A, the GH1 gene is... | Download Scientific Diagram](https://www.researchgate.net/publication/5268659/figure/fig1/AS:456132213907456@1485761802452/GH1-gene-structure-and-disease-causing-mutations-A-the-GH1-gene-is-composed-of-five.png)
GH1 gene structure and disease causing mutations. A, the GH1 gene is... | Download Scientific Diagram
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GH1 deletion analysis of intron 2-exon 3-intron 3. A, The position and... | Download Scientific Diagram
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Human growth hormone (GH1) gene polymorphism map in a normal-statured adult population – ScienceOpen
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Genetic causes and treatment of isolated growth hormone deficiency—an update | Nature Reviews Endocrinology
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Prevalence of Human GH-1 Gene Alterations in Patients with Isolated Growth Hormone Deficiency | Pediatric Research
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Decreased Activity of the Ghrhr and Gh Promoters Causes Dominantly Inherited GH Deficiency | bioRxiv
![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
![Schematic representation of the human GH1 gene showing the alternative... | Download Scientific Diagram Schematic representation of the human GH1 gene showing the alternative... | Download Scientific Diagram](https://www.researchgate.net/publication/6428892/figure/fig1/AS:601782216577025@1520487469239/Schematic-representation-of-the-human-GH1-gene-showing-the-alternative-splicing-of-exon.png)
Schematic representation of the human GH1 gene showing the alternative... | Download Scientific Diagram
![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)
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