متلازمة هانهارت (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "متلازمة هانهارت" in Arabic language version.

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9web.archive.org

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6nih.gov

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3doi.org

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3semanticscholar.org

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2rarediseases.org

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1ncsu.edu

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1omim.org

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1orpha.net

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1independent.co.uk

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1ajol.info

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1worldcat.org

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1mhmedical.com

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ajol.info

Varal IG, Dogan P (29 Apr 2019). "Hanhart syndrome: hypoglossia-hypodactylia syndrome". Pan African Medical Journal (بالإنجليزية). 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 (أبريل 1976). "Studies of malformation syndromes of man XXXXI B: nosologic studies in the Hanhart and the Möbius syndrome". European Journal of Pediatrics. ج. 122 ع. 1: 19–55. DOI:10.1007/BF00445030. PMID:1261566. S2CID:23498856.
Bersu ET، Pettersen JC، Charboneau WJ، Opitz JM (أبريل 1976). "Studies of malformation syndromes of man XXXXIA: anatomical studies in the Hanhart syndrome--a pathogenetic hypothesis". European Journal of Pediatrics. ج. 122 ع. 1: 1–17. DOI:10.1007/BF00445029. PMID:1261565. S2CID:10440385.
Bökesoy I، Aksüyek C، Deniz E (يوليو 1983). "Oromandibular limb hypogenesis/Hanhart's syndrome: possible drug influence on the malformation". Clinical Genetics. ج. 24 ع. 1: 47–49. DOI:10.1111/j.1399-0004.1983.tb00068.x. PMID:6616945. S2CID:43535751.

independent.co.uk

Petter O (20 يوليو 2017). "Bodybuilder with one arm and no legs becomes internet sensation". ذي إندبندنت. مؤرشف من الأصل في 2018-04-19. اطلع عليه بتاريخ 2018-04-19.

mhmedical.com

accessanesthesiology.mhmedical.com

Bissonnette، Bruno؛ Luginbuehl، Igor؛ Engelhardt، Thomas (2019)، "Hypoglossia-Hypodactylia Syndrome"، Syndromes: Rapid Recognition and Perioperative Implications (ط. 2)، New York, NY: McGraw-Hill Education، مؤرشف من الأصل في 2023-03-10، اطلع عليه بتاريخ 2023-02-27

ncsu.edu

rarediseases.oscar.ncsu.edu

"Hypoglossia-hypodactyly syndrome". Rare Diseases Infohub. مؤرشف من الأصل في 2023-02-25. اطلع عليه بتاريخ 2023-03-10.

nih.gov

pubmed.ncbi.nlm.nih.gov

Herrmann J، Pallister PD، Gilbert EF، Vieseskul C، Bersu E، Pettersen JC، Opitz JM (أبريل 1976). "Studies of malformation syndromes of man XXXXI B: nosologic studies in the Hanhart and the Möbius syndrome". European Journal of Pediatrics. ج. 122 ع. 1: 19–55. DOI:10.1007/BF00445030. PMID:1261566. S2CID:23498856.
Bersu ET، Pettersen JC، Charboneau WJ، Opitz JM (أبريل 1976). "Studies of malformation syndromes of man XXXXIA: anatomical studies in the Hanhart syndrome--a pathogenetic hypothesis". European Journal of Pediatrics. ج. 122 ع. 1: 1–17. DOI:10.1007/BF00445029. PMID:1261565. S2CID:10440385.
Varal IG, Dogan P (29 Apr 2019). "Hanhart syndrome: hypoglossia-hypodactylia syndrome". Pan African Medical Journal (بالإنجليزية). 32 (1): 213. ISSN:1937-8688. PMC:6620079. PMID:31312325. Archived from the original on 2023-02-26. Retrieved 2023-03-10.
Bökesoy I، Aksüyek C، Deniz E (يوليو 1983). "Oromandibular limb hypogenesis/Hanhart's syndrome: possible drug influence on the malformation". Clinical Genetics. ج. 24 ع. 1: 47–49. DOI:10.1111/j.1399-0004.1983.tb00068.x. PMID:6616945. S2CID:43535751.

rarediseases.info.nih.gov

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

ncbi.nlm.nih.gov

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

omim.org

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

orpha.net

"Orphanet: Hypoglossia hypodactyly syndrome". www.orpha.net. مؤرشف من الأصل في 2023-02-25. اطلع عليه بتاريخ 2023-02-25.

rarediseases.org

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

semanticscholar.org

api.semanticscholar.org

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

web.archive.org

"Hanhart syndrome - National Organization for Rare Disorders". rarediseases.org (بAmerican English). 16 Jun 2022. Archived from the original on 2023-02-25. Retrieved 2023-02-25.
"Hypoglossia-hypodactyly syndrome". Rare Diseases Infohub. مؤرشف من الأصل في 2023-02-25. اطلع عليه بتاريخ 2023-03-10.
"Hanhart Syndrome - National Organization for Rare Disorders". rarediseases.org (بAmerican English). Archived from the original on 2021-09-30. Retrieved 2023-02-25.
McKusick VA, Kniffin CL (8 Aug 2016). "Hypoglossia-Hypodactylia". omim.org (بAmerican English). Archived from the original on 2022-06-17. Retrieved 2023-02-25.
"Orphanet: Hypoglossia hypodactyly syndrome". www.orpha.net. مؤرشف من الأصل في 2023-02-25. اطلع عليه بتاريخ 2023-02-25.
"Hanhart syndrome - About the Disease - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov (بالإنجليزية). Archived from the original on 2023-01-05. Retrieved 2023-02-25.
Petter O (20 يوليو 2017). "Bodybuilder with one arm and no legs becomes internet sensation". ذي إندبندنت. مؤرشف من الأصل في 2018-04-19. اطلع عليه بتاريخ 2018-04-19.
Varal IG, Dogan P (29 Apr 2019). "Hanhart syndrome: hypoglossia-hypodactylia syndrome". Pan African Medical Journal (بالإنجليزية). 32 (1): 213. ISSN:1937-8688. PMC:6620079. PMID:31312325. Archived from the original on 2023-02-26. Retrieved 2023-03-10.
Bissonnette، Bruno؛ Luginbuehl، Igor؛ Engelhardt، Thomas (2019)، "Hypoglossia-Hypodactylia Syndrome"، Syndromes: Rapid Recognition and Perioperative Implications (ط. 2)، New York, NY: McGraw-Hill Education، مؤرشف من الأصل في 2023-03-10، اطلع عليه بتاريخ 2023-02-27

worldcat.org

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