![Homozygous deletion of SHOX in a mentally retarded male with Langer mesomelic dysplasia | Journal of Medical Genetics Homozygous deletion of SHOX in a mentally retarded male with Langer mesomelic dysplasia | Journal of Medical Genetics](https://jmg.bmj.com/content/jmedgenet/37/12/959/F3.large.jpg)
Homozygous deletion of SHOX in a mentally retarded male with Langer mesomelic dysplasia | Journal of Medical Genetics
![University student had arms SLICED open by doctors after rare condition cut off blood supply and turned her hands blue | The Sun University student had arms SLICED open by doctors after rare condition cut off blood supply and turned her hands blue | The Sun](https://www.thesun.co.uk/wp-content/uploads/2018/12/NINTCHDBPICT000458544307.jpg)
University student had arms SLICED open by doctors after rare condition cut off blood supply and turned her hands blue | The Sun
![Flail arm syndrome: a distinctive variant of amyotrophic lateral sclerosis | Journal of Neurology, Neurosurgery & Psychiatry Flail arm syndrome: a distinctive variant of amyotrophic lateral sclerosis | Journal of Neurology, Neurosurgery & Psychiatry](https://jnnp.bmj.com/content/jnnp/65/6/950/F1.large.jpg)
Flail arm syndrome: a distinctive variant of amyotrophic lateral sclerosis | Journal of Neurology, Neurosurgery & Psychiatry
![Patient with deletion of short arm of chromosome 18, note cebocephaly... | Download Scientific Diagram Patient with deletion of short arm of chromosome 18, note cebocephaly... | Download Scientific Diagram](https://www.researchgate.net/publication/49602438/figure/fig1/AS:305951379869707@1449955901831/Patient-with-deletion-of-short-arm-of-chromosome-18-note-cebocephaly-and-ocular.png)
Patient with deletion of short arm of chromosome 18, note cebocephaly... | Download Scientific Diagram
Down Syndrome Association Nepal (DSAN) - Wolf-Hirschhorn syndrome (WHS) is an extremely rare chromosomal disorder caused by a missing part (deletion) of the short arm(“p”)of chromosome 4. Each chromosome has a short
![Microcephaly, short stature, and limb abnormality disorder due to novel autosomal biallelic DONSON mutations in two German siblings | European Journal of Human Genetics Microcephaly, short stature, and limb abnormality disorder due to novel autosomal biallelic DONSON mutations in two German siblings | European Journal of Human Genetics](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41431-018-0128-0/MediaObjects/41431_2018_128_Fig1_HTML.jpg)
Microcephaly, short stature, and limb abnormality disorder due to novel autosomal biallelic DONSON mutations in two German siblings | European Journal of Human Genetics
![تويتر \ Rosh Review على تويتر: "Which syndrome is assoc w/ a terminal deletion short arm chromosome 5? #RoshQuiz #FOAMpeds #FOAMed #PANCE #FMRevolution #NursePractitioner https://t.co/cgiapiCZoo" تويتر \ Rosh Review على تويتر: "Which syndrome is assoc w/ a terminal deletion short arm chromosome 5? #RoshQuiz #FOAMpeds #FOAMed #PANCE #FMRevolution #NursePractitioner https://t.co/cgiapiCZoo"](https://pbs.twimg.com/media/C4JdM1jXAAA9sdp.jpg)