Langer–Giedion syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Langer–Giedion syndrome" in English language version.

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3rarediseases.org

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2semanticscholar.org

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1indianpediatrics.net

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1medlineplus.gov

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doi.org

McBrien, J.; Crolla, J. A.; Huang, S.; Kelleher, J.; Gleeson, J.; Lynch, S. A. (June 2008). "Further case of microdeletion of 8q24 with phenotype overlapping Langer–Giedion withoutTRPS1 deletion". American Journal of Medical Genetics Part A. 146A (12): 1587–1592. doi:10.1002/ajmg.a.32347. PMID 18478595. S2CID 19384557.
Albert Schinzel; Mariluce Riegel (2013). "Long-term follow-up of four patients with Langer–Giedion syndrome". American Journal of Medical Genetics Part A. 161 (9): 2216–2225. doi:10.1002/ajmg.a.36062. PMID 23913778. S2CID 26579346.

indianpediatrics.net

Devidayal; Marwaha RK (February 2006). "Langer–Giedion Syndrome" (PDF). Indian Pediatrics. 43 (2): 174–175. PMID 16528117.

medlineplus.gov

"trichorhinophalangeal syndrome type II". MedlinePlus. Retrieved July 7, 2021.

nih.gov

pubmed.ncbi.nlm.nih.gov

McBrien, J.; Crolla, J. A.; Huang, S.; Kelleher, J.; Gleeson, J.; Lynch, S. A. (June 2008). "Further case of microdeletion of 8q24 with phenotype overlapping Langer–Giedion withoutTRPS1 deletion". American Journal of Medical Genetics Part A. 146A (12): 1587–1592. doi:10.1002/ajmg.a.32347. PMID 18478595. S2CID 19384557.
Devidayal; Marwaha RK (February 2006). "Langer–Giedion Syndrome" (PDF). Indian Pediatrics. 43 (2): 174–175. PMID 16528117.
Albert Schinzel; Mariluce Riegel (2013). "Long-term follow-up of four patients with Langer–Giedion syndrome". American Journal of Medical Genetics Part A. 161 (9): 2216–2225. doi:10.1002/ajmg.a.36062. PMID 23913778. S2CID 26579346.

rarediseases.info.nih.gov

"trichorhinophalangeal syndrome type 2". Genetic and Rare Diseases Information Center. Retrieved July 7, 2021.

omim.org

rarediseases.org

"Trichorhinophalangeal syndrome type ii". National Organisation for Rare Disorders. Retrieved July 7, 2021.
"Trichorhinophalangeal syndrome type ii". National Organisation for Rare Disorders. Retrieved July 7, 2021.
"trichorhinophalangeal syndrome type ii". National Organisation for Rare Disorders. Retrieved July 2, 2021.

semanticscholar.org

api.semanticscholar.org

McBrien, J.; Crolla, J. A.; Huang, S.; Kelleher, J.; Gleeson, J.; Lynch, S. A. (June 2008). "Further case of microdeletion of 8q24 with phenotype overlapping Langer–Giedion withoutTRPS1 deletion". American Journal of Medical Genetics Part A. 146A (12): 1587–1592. doi:10.1002/ajmg.a.32347. PMID 18478595. S2CID 19384557.
Albert Schinzel; Mariluce Riegel (2013). "Long-term follow-up of four patients with Langer–Giedion syndrome". American Journal of Medical Genetics Part A. 161 (9): 2216–2225. doi:10.1002/ajmg.a.36062. PMID 23913778. S2CID 26579346.

wiley.com

onlinelibrary.wiley.com

Albert Schinzel; Mariluce Riegel (2013). "Long-term follow-up of four patients with Langer–Giedion syndrome". American Journal of Medical Genetics Part A. 161 (9): 2216–2225. doi:10.1002/ajmg.a.36062. PMID 23913778. S2CID 26579346.