JMSCR Volume||2||Issue||11||Page 2837-2840||November-2014 Langer Giedion Syndrome with Absence of Bilateral Radial Arteries –
![Tetraparesis due to exostotic osteochondroma at upper cervical cord in a patient with multiple exostoses–mental retardation syndrome (Langer–Giedion syndrome) | Spinal Cord Tetraparesis due to exostotic osteochondroma at upper cervical cord in a patient with multiple exostoses–mental retardation syndrome (Langer–Giedion syndrome) | Spinal Cord](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fsj.sc.3101690/MediaObjects/41393_2005_Article_BF3101690_Fig1_HTML.jpg)
Tetraparesis due to exostotic osteochondroma at upper cervical cord in a patient with multiple exostoses–mental retardation syndrome (Langer–Giedion syndrome) | Spinal Cord
Nationwide Children's Hospital - Mile 10 - Kolby Langer Giedion Syndrome Find out how you can help support kids like Kolby: http://goo.gl/bu1RmO | Facebook
Síndrome de Langer-Giedion con deleción 8q23.1-q24.12, diagnosticado por hibridación genómica comparativa
![Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3–q24.11 and 8q24.13 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT1 ... Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3–q24.11 and 8q24.13 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT1 ...](https://ars.els-cdn.com/content/image/1-s2.0-S1028455915001710-gr3.jpg)
Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3–q24.11 and 8q24.13 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT1 ...
![An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4 | Molecular Cytogenetics | Full Text An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4 | Molecular Cytogenetics | Full Text](https://media.springernature.com/m685/springer-static/image/art%3A10.1186%2Fs13039-015-0169-9/MediaObjects/13039_2015_169_Fig2_HTML.gif)
An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4 | Molecular Cytogenetics | Full Text
![PDF] Trichorhinophalangeal syndrome type II presenting with short stature in a child. | Semantic Scholar PDF] Trichorhinophalangeal syndrome type II presenting with short stature in a child. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/763e4ac0857a64ffb0c69e110c7304e7dde13a9c/2-Figure1-1.png)
PDF] Trichorhinophalangeal syndrome type II presenting with short stature in a child. | Semantic Scholar
![An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4 | Molecular Cytogenetics | Full Text An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4 | Molecular Cytogenetics | Full Text](https://media.springernature.com/full/springer-static/image/art%3A10.1186%2Fs13039-015-0169-9/MediaObjects/13039_2015_169_Fig1_HTML.gif)