Hanhart syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Hanhart syndrome" in English language version.

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10nih.gov

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9web.archive.org

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6doi.org

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3semanticscholar.org

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2rarediseases.org

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2worldcat.org

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1omim.org

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1orpha.net

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1ajol.info

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1mhmedical.com

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1independent.co.uk

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1today.com

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ajol.info

Varal IG, Dogan P (2019-04-29). "Hanhart syndrome: hypoglossia-hypodactylia syndrome". Pan African Medical Journal. 32 (1): 213. ISSN 1937-8688. PMC 6620079. PMID 31312325. Archived from the original on 2023-02-26. Retrieved 2023-03-10.

doi.org

Herrmann J, Pallister PD, Gilbert EF, Vieseskul C, Bersu E, Pettersen JC, Opitz JM (April 1976). "Studies of malformation syndromes of man XXXXI B: nosologic studies in the Hanhart and the Möbius syndrome". European Journal of Pediatrics. 122 (1): 19–55. doi:10.1007/BF00445030. PMID 1261566. S2CID 23498856.
Gathwala G, Singh J, Dalal P, Garg A (March 2011). "Hypoglossia-hypodactyly syndrome in a newborn". Journal of Cranio-Maxillo-Facial Surgery. 39 (2): 99–101. doi:10.1016/j.jcms.2010.06.007. PMID 20673638.
Goyal M, Singh A, Singh P, Kapoor S (April 2014). "Hypoglossia-hypodactyly syndrome with short stature - a case report". Journal of Clinical and Diagnostic Research. 8 (4): SD01–SD02. doi:10.7860/JCDR/2014/7809.4281 (inactive 1 November 2024). PMC 4064859. PMID 24959494.{{cite journal}}: CS1 maint: DOI inactive as of November 2024 (link)
Bersu ET, Pettersen JC, Charboneau WJ, Opitz JM (April 1976). "Studies of malformation syndromes of man XXXXIA: anatomical studies in the Hanhart syndrome--a pathogenetic hypothesis". European Journal of Pediatrics. 122 (1): 1–17. doi:10.1007/BF00445029. PMID 1261565. S2CID 10440385.
Bökesoy I, Aksüyek C, Deniz E (July 1983). "Oromandibular limb hypogenesis/Hanhart's syndrome: possible drug influence on the malformation". Clinical Genetics. 24 (1): 47–49. doi:10.1111/j.1399-0004.1983.tb00068.x. PMID 6616945. S2CID 43535751.
Chen, C. P.; Liu, F. F.; Jan, S. W.; Lin, S. P.; Lan, C. C. (1996-06-14). "CVS-exposed limb deficiency defects with or without other birth defects: presentation of six cases born during a period of nine years". American Journal of Medical Genetics. 63 (3): 447–453. doi:10.1002/(SICI)1096-8628(19960614)63:3<447::AID-AJMG6>3.0.CO;2-O. ISSN 0148-7299. PMID 8737650.

independent.co.uk

Petter O (20 July 2017). "Bodybuilder with one arm and no legs becomes internet sensation". The Independent. Archived from the original on 19 April 2018. Retrieved 19 April 2018.

mhmedical.com

accessanesthesiology.mhmedical.com

Bissonnette, Bruno; Luginbuehl, Igor; Engelhardt, Thomas (2019), "Hypoglossia-Hypodactylia Syndrome", Syndromes: Rapid Recognition and Perioperative Implications (2 ed.), New York, NY: McGraw-Hill Education, archived from the original on 2023-03-10, retrieved 2023-02-27

nih.gov

pubmed.ncbi.nlm.nih.gov

Herrmann J, Pallister PD, Gilbert EF, Vieseskul C, Bersu E, Pettersen JC, Opitz JM (April 1976). "Studies of malformation syndromes of man XXXXI B: nosologic studies in the Hanhart and the Möbius syndrome". European Journal of Pediatrics. 122 (1): 19–55. doi:10.1007/BF00445030. PMID 1261566. S2CID 23498856.
Gathwala G, Singh J, Dalal P, Garg A (March 2011). "Hypoglossia-hypodactyly syndrome in a newborn". Journal of Cranio-Maxillo-Facial Surgery. 39 (2): 99–101. doi:10.1016/j.jcms.2010.06.007. PMID 20673638.
Varal IG, Dogan P (2019-04-29). "Hanhart syndrome: hypoglossia-hypodactylia syndrome". Pan African Medical Journal. 32 (1): 213. ISSN 1937-8688. PMC 6620079. PMID 31312325. Archived from the original on 2023-02-26. Retrieved 2023-03-10.
Goyal M, Singh A, Singh P, Kapoor S (April 2014). "Hypoglossia-hypodactyly syndrome with short stature - a case report". Journal of Clinical and Diagnostic Research. 8 (4): SD01–SD02. doi:10.7860/JCDR/2014/7809.4281 (inactive 1 November 2024). PMC 4064859. PMID 24959494.{{cite journal}}: CS1 maint: DOI inactive as of November 2024 (link)
Bersu ET, Pettersen JC, Charboneau WJ, Opitz JM (April 1976). "Studies of malformation syndromes of man XXXXIA: anatomical studies in the Hanhart syndrome--a pathogenetic hypothesis". European Journal of Pediatrics. 122 (1): 1–17. doi:10.1007/BF00445029. PMID 1261565. S2CID 10440385.
Bökesoy I, Aksüyek C, Deniz E (July 1983). "Oromandibular limb hypogenesis/Hanhart's syndrome: possible drug influence on the malformation". Clinical Genetics. 24 (1): 47–49. doi:10.1111/j.1399-0004.1983.tb00068.x. PMID 6616945. S2CID 43535751.
Chen, C. P.; Liu, F. F.; Jan, S. W.; Lin, S. P.; Lan, C. C. (1996-06-14). "CVS-exposed limb deficiency defects with or without other birth defects: presentation of six cases born during a period of nine years". American Journal of Medical Genetics. 63 (3): 447–453. doi:10.1002/(SICI)1096-8628(19960614)63:3<447::AID-AJMG6>3.0.CO;2-O. ISSN 0148-7299. PMID 8737650.

ncbi.nlm.nih.gov

Varal IG, Dogan P (2019-04-29). "Hanhart syndrome: hypoglossia-hypodactylia syndrome". Pan African Medical Journal. 32 (1): 213. ISSN 1937-8688. PMC 6620079. PMID 31312325. Archived from the original on 2023-02-26. Retrieved 2023-03-10.
Goyal M, Singh A, Singh P, Kapoor S (April 2014). "Hypoglossia-hypodactyly syndrome with short stature - a case report". Journal of Clinical and Diagnostic Research. 8 (4): SD01–SD02. doi:10.7860/JCDR/2014/7809.4281 (inactive 1 November 2024). PMC 4064859. PMID 24959494.{{cite journal}}: CS1 maint: DOI inactive as of November 2024 (link)

rarediseases.info.nih.gov

"Hanhart syndrome - About the Disease - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Archived from the original on 2023-01-05. Retrieved 2023-02-25.

omim.org

McKusick VA, Kniffin CL (August 8, 2016). "Hypoglossia-Hypodactylia". omim.org. Archived from the original on 2022-06-17. Retrieved 2023-02-25.

orpha.net

"Orphanet: Hypoglossia hypodactyly syndrome". www.orpha.net. Archived from the original on 2023-02-25. Retrieved 2023-02-25.

rarediseases.org

"Hanhart Syndrome - National Organization for Rare Disorders". rarediseases.org. Archived from the original on 2021-09-30. Retrieved 2023-02-25.
"Hanhart syndrome - National Organization for Rare Disorders". rarediseases.org. 2022-06-16. Archived from the original on 2023-02-25. Retrieved 2023-02-25.

semanticscholar.org

api.semanticscholar.org

Herrmann J, Pallister PD, Gilbert EF, Vieseskul C, Bersu E, Pettersen JC, Opitz JM (April 1976). "Studies of malformation syndromes of man XXXXI B: nosologic studies in the Hanhart and the Möbius syndrome". European Journal of Pediatrics. 122 (1): 19–55. doi:10.1007/BF00445030. PMID 1261566. S2CID 23498856.
Bersu ET, Pettersen JC, Charboneau WJ, Opitz JM (April 1976). "Studies of malformation syndromes of man XXXXIA: anatomical studies in the Hanhart syndrome--a pathogenetic hypothesis". European Journal of Pediatrics. 122 (1): 1–17. doi:10.1007/BF00445029. PMID 1261565. S2CID 10440385.
Bökesoy I, Aksüyek C, Deniz E (July 1983). "Oromandibular limb hypogenesis/Hanhart's syndrome: possible drug influence on the malformation". Clinical Genetics. 24 (1): 47–49. doi:10.1111/j.1399-0004.1983.tb00068.x. PMID 6616945. S2CID 43535751.

today.com

Stump S (October 2016). "'Dead' man living: Disabled teen-turned-Internet star 'lives by inspiring others'". Today. Archived from the original on 2018-04-19. Retrieved 2018-04-19.

web.archive.org

"Hanhart Syndrome - National Organization for Rare Disorders". rarediseases.org. Archived from the original on 2021-09-30. Retrieved 2023-02-25.
"Hanhart syndrome - National Organization for Rare Disorders". rarediseases.org. 2022-06-16. Archived from the original on 2023-02-25. Retrieved 2023-02-25.
McKusick VA, Kniffin CL (August 8, 2016). "Hypoglossia-Hypodactylia". omim.org. Archived from the original on 2022-06-17. Retrieved 2023-02-25.
"Orphanet: Hypoglossia hypodactyly syndrome". www.orpha.net. Archived from the original on 2023-02-25. Retrieved 2023-02-25.
Varal IG, Dogan P (2019-04-29). "Hanhart syndrome: hypoglossia-hypodactylia syndrome". Pan African Medical Journal. 32 (1): 213. ISSN 1937-8688. PMC 6620079. PMID 31312325. Archived from the original on 2023-02-26. Retrieved 2023-03-10.
"Hanhart syndrome - About the Disease - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Archived from the original on 2023-01-05. Retrieved 2023-02-25.
Bissonnette, Bruno; Luginbuehl, Igor; Engelhardt, Thomas (2019), "Hypoglossia-Hypodactylia Syndrome", Syndromes: Rapid Recognition and Perioperative Implications (2 ed.), New York, NY: McGraw-Hill Education, archived from the original on 2023-03-10, retrieved 2023-02-27
Petter O (20 July 2017). "Bodybuilder with one arm and no legs becomes internet sensation". The Independent. Archived from the original on 19 April 2018. Retrieved 19 April 2018.
Stump S (October 2016). "'Dead' man living: Disabled teen-turned-Internet star 'lives by inspiring others'". Today. Archived from the original on 2018-04-19. Retrieved 2018-04-19.

worldcat.org

search.worldcat.org

Varal IG, Dogan P (2019-04-29). "Hanhart syndrome: hypoglossia-hypodactylia syndrome". Pan African Medical Journal. 32 (1): 213. ISSN 1937-8688. PMC 6620079. PMID 31312325. Archived from the original on 2023-02-26. Retrieved 2023-03-10.
Chen, C. P.; Liu, F. F.; Jan, S. W.; Lin, S. P.; Lan, C. C. (1996-06-14). "CVS-exposed limb deficiency defects with or without other birth defects: presentation of six cases born during a period of nine years". American Journal of Medical Genetics. 63 (3): 447–453. doi:10.1002/(SICI)1096-8628(19960614)63:3<447::AID-AJMG6>3.0.CO;2-O. ISSN 0148-7299. PMID 8737650.