![Allgrove Syndrome in Iranian Patients and Report on a Novel Mutation in AAAS Gene | Iranian Journal of Pediatrics | Full Text Allgrove Syndrome in Iranian Patients and Report on a Novel Mutation in AAAS Gene | Iranian Journal of Pediatrics | Full Text](http://services.brieflands.com/cdn/serve/3144b/8571ae499779df594403cc172eba3908ed87ccd5/ijp-In_Press-In_Press-6921-i002-preview.png)
Allgrove Syndrome in Iranian Patients and Report on a Novel Mutation in AAAS Gene | Iranian Journal of Pediatrics | Full Text
![Triple A (Allgrove) syndrome due to AAAS gene mutation with a rare association of amyotrophy | SpringerLink Triple A (Allgrove) syndrome due to AAAS gene mutation with a rare association of amyotrophy | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs42000-020-00217-7/MediaObjects/42000_2020_217_Fig2_HTML.png)
Triple A (Allgrove) syndrome due to AAAS gene mutation with a rare association of amyotrophy | SpringerLink
![PDF) Mutation Spectra of the AAAS Gene in Iranian Families with Allgrove Syndrome | ziba soltani - Academia.edu PDF) Mutation Spectra of the AAAS Gene in Iranian Families with Allgrove Syndrome | ziba soltani - Academia.edu](https://0.academia-photos.com/attachment_thumbnails/49971264/mini_magick20190130-22168-1wqwid9.png?1548847318)
PDF) Mutation Spectra of the AAAS Gene in Iranian Families with Allgrove Syndrome | ziba soltani - Academia.edu
![AAAS on X: "Although attention has been directed to the X and Y sex #chromosomes, we do not understand how sex affects the rest of the #genome. Research published in @ScienceMagazine last AAAS on X: "Although attention has been directed to the X and Y sex #chromosomes, we do not understand how sex affects the rest of the #genome. Research published in @ScienceMagazine last](https://pbs.twimg.com/media/EAqBgRgXUAAwkfK.jpg)
AAAS on X: "Although attention has been directed to the X and Y sex #chromosomes, we do not understand how sex affects the rest of the #genome. Research published in @ScienceMagazine last
![Clinical and molecular report of c.1331 + 1G > A mutation of the AAAS gene in a Moroccan family with Allgrove syndrome: a case report | BMC Pediatrics | Full Text Clinical and molecular report of c.1331 + 1G > A mutation of the AAAS gene in a Moroccan family with Allgrove syndrome: a case report | BMC Pediatrics | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs12887-018-1161-4/MediaObjects/12887_2018_1161_Fig3_HTML.png)
Clinical and molecular report of c.1331 + 1G > A mutation of the AAAS gene in a Moroccan family with Allgrove syndrome: a case report | BMC Pediatrics | Full Text
![Identification of AAAS gene mutation in Allgrove syndrome: A report of three cases | Semantic Scholar Identification of AAAS gene mutation in Allgrove syndrome: A report of three cases | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/e4825d2ead6e71f3507e9f72495c867b87b03887/4-Figure3-1.png)
Identification of AAAS gene mutation in Allgrove syndrome: A report of three cases | Semantic Scholar
![Sequencing of the AAAS gene. Novel homozygous mutation: IVS7+1 G to A.... | Download Scientific Diagram Sequencing of the AAAS gene. Novel homozygous mutation: IVS7+1 G to A.... | Download Scientific Diagram](https://www.researchgate.net/publication/234834239/figure/fig1/AS:299778081607680@1448484072268/Sequencing-of-the-AAAS-gene-Novel-homozygous-mutation-IVS7-1-G-to-A-The-parents-were.png)
Sequencing of the AAAS gene. Novel homozygous mutation: IVS7+1 G to A.... | Download Scientific Diagram
![Allgrove Syndrome in Iranian Patients and Report on a Novel Mutation in AAAS Gene | Iranian Journal of Pediatrics | Full Text Allgrove Syndrome in Iranian Patients and Report on a Novel Mutation in AAAS Gene | Iranian Journal of Pediatrics | Full Text](http://services.brieflands.com/cdn/serve/3144b/1562b4cde7fd24184cbd68718cbb5a64bee68eeb/ijp-In_Press-In_Press-6921-i001-preview.png)
Allgrove Syndrome in Iranian Patients and Report on a Novel Mutation in AAAS Gene | Iranian Journal of Pediatrics | Full Text
![Triple A (Allgrove) syndrome: an unusual association with syringomyelia – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open science hub. Triple A (Allgrove) syndrome: an unusual association with syringomyelia – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open science hub.](https://cyberleninka.org/viewer_images/551065/f/1.png)
Triple A (Allgrove) syndrome: an unusual association with syringomyelia – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open science hub.
![Schematic representation of the AAAS gene and the published mutations... | Download Scientific Diagram Schematic representation of the AAAS gene and the published mutations... | Download Scientific Diagram](https://www.researchgate.net/publication/262021183/figure/fig2/AS:296932326035463@1447805591880/Schematic-representation-of-the-AAAS-gene-and-the-published-mutations-to-date-1-5.png)
Schematic representation of the AAAS gene and the published mutations... | Download Scientific Diagram
![Identification of AAAS gene mutation in Allgrove syndrome: A report of three cases | Semantic Scholar Identification of AAAS gene mutation in Allgrove syndrome: A report of three cases | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/e4825d2ead6e71f3507e9f72495c867b87b03887/3-Figure1-1.png)
Identification of AAAS gene mutation in Allgrove syndrome: A report of three cases | Semantic Scholar
![Phenotype–genotype spectrum of AAA syndrome from Western India and systematic review of literature in: Endocrine Connections Volume 6 Issue 8 (2017) Phenotype–genotype spectrum of AAA syndrome from Western India and systematic review of literature in: Endocrine Connections Volume 6 Issue 8 (2017)](https://ec.bioscientifica.com/view/journals/ec/6/8/images/EC-17-0255fig1.jpeg)