Jordan's Guardian Angels - "It's been 2 years since we got the most bitter sweet phone call of our lives. Within an hour, we were “accepted” by Jordan's Guardian Angels on Facebook
![A Novel Missense Variant in the Gene PPP2R5D Causes a Rare Neurodevelopmental Disorder with Increased Phenotype A Novel Missense Variant in the Gene PPP2R5D Causes a Rare Neurodevelopmental Disorder with Increased Phenotype](https://static-02.hindawi.com/articles/bmri/volume-2021/6661860/figures/6661860.fig.001d.jpg)
A Novel Missense Variant in the Gene PPP2R5D Causes a Rare Neurodevelopmental Disorder with Increased Phenotype
![Jordan's Syndrome on Twitter: "Happy Midsummer from our family from Sweden!! #ppp2r5d #jordanssyndrome #jordansguardianangels #midsummer2018 https://t.co/i7g4n9WuDl" / Twitter Jordan's Syndrome on Twitter: "Happy Midsummer from our family from Sweden!! #ppp2r5d #jordanssyndrome #jordansguardianangels #midsummer2018 https://t.co/i7g4n9WuDl" / Twitter](https://pbs.twimg.com/media/DgULVb8UwAAYm-V.jpg)
Jordan's Syndrome on Twitter: "Happy Midsummer from our family from Sweden!! #ppp2r5d #jordanssyndrome #jordansguardianangels #midsummer2018 https://t.co/i7g4n9WuDl" / Twitter
![Jordan's Syndrome on Twitter: "Meet Katelyn from California, USA https://t.co/VJ1pfXTZwJ #ppp2r5d #jordanssyndrome #meetourfamily #raregenetics https://t.co/dNnhJdZ81e" / Twitter Jordan's Syndrome on Twitter: "Meet Katelyn from California, USA https://t.co/VJ1pfXTZwJ #ppp2r5d #jordanssyndrome #meetourfamily #raregenetics https://t.co/dNnhJdZ81e" / Twitter](https://pbs.twimg.com/media/DLdb-TZW4AArN28.jpg)
Jordan's Syndrome on Twitter: "Meet Katelyn from California, USA https://t.co/VJ1pfXTZwJ #ppp2r5d #jordanssyndrome #meetourfamily #raregenetics https://t.co/dNnhJdZ81e" / Twitter
![A Novel Missense Variant in the Gene PPP2R5D Causes a Rare Neurodevelopmental Disorder with Increased Phenotype A Novel Missense Variant in the Gene PPP2R5D Causes a Rare Neurodevelopmental Disorder with Increased Phenotype](https://static-02.hindawi.com/articles/bmri/volume-2021/6661860/figures/6661860.fig.001b.jpg)
A Novel Missense Variant in the Gene PPP2R5D Causes a Rare Neurodevelopmental Disorder with Increased Phenotype
![PDF) PPP2R5D-Related Intellectual Disability and Neurodevelopmental Delay: A Review of the Current Understanding of the Genetics and Biochemical Basis of the Disorder PDF) PPP2R5D-Related Intellectual Disability and Neurodevelopmental Delay: A Review of the Current Understanding of the Genetics and Biochemical Basis of the Disorder](https://i1.rgstatic.net/publication/339361130_PPP2R5D-Related_Intellectual_Disability_and_Neurodevelopmental_Delay_A_Review_of_the_Current_Understanding_of_the_Genetics_and_Biochemical_Basis_of_the_Disorder/links/5e4d3e4b92851c7f7f45c54a/largepreview.png)
PDF) PPP2R5D-Related Intellectual Disability and Neurodevelopmental Delay: A Review of the Current Understanding of the Genetics and Biochemical Basis of the Disorder
Jordan's Syndrome” PPP2R5D Prospectus Executive Summary Mutations in the gene PPP2R5D have recently been described as a
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