SCARF syndrome (English Wikipedia)

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

refsWebsite

Global rank English rank

5nih.gov

4^th place

4orpha.net

3,537^th place

7,177^th place

2web.archive.org

1^st place

2doi.org

2^nd place

2worldcat.org

5^th place

1malacards.org

low place

1omim.org

4,380^th place

4,305^th place

1aoa.org

low place

1cdc.gov

218^th place

212^th place

1wiley.com

222^nd place

297^th place

1dovemed.com

low place

1medlineplus.gov

1,581^st place

1,299^th place

aoa.org

"Strabismus (crossed eyes)". www.aoa.org. Retrieved 2020-12-16.

cdc.gov

CDC (2019-12-04). "Facts about Craniosynostosis | CDC". Centers for Disease Control and Prevention. Retrieved 2020-12-16.

doi.org

Rahimpour, Masoume; Sohrabi, Mohammad bager; Kalhor, Sulmaz; Khosravi, Hossein ali; Zolfaghari, Poone; Yahyaei, Elahe (2014-03-16). "A rare case report: SCARF syndrome". Clinical Case Reports. 2 (3): 74–76. doi:10.1002/ccr3.61. ISSN 2050-0904. PMC 4184596. PMID 25356252.
Koppe, Roswitha; Kaplan, Paige; Hunter, Alasdair; MacMurray, Brock (1989). "Ambiguous genitalia associated with skeletal abnormalities, cutis laxa, craniostenosis, psychomotor retardation, and facial abnormalities (SCARF syndrome)". American Journal of Medical Genetics. 34 (3): 305–312. doi:10.1002/ajmg.1320340302. ISSN 1096-8628. PMID 2596519.

dovemed.com

Purohit, Maulik (2018-04-28). "SCARF Syndrome". www.dovemed.com. Retrieved 2020-11-11.

malacards.org

"Scarf Syndrome disease: Malacards – Research Articles, Drugs, Genes, Clinical Trials". www.malacards.org. Retrieved 2020-11-05.

medlineplus.gov

"Cutis laxa: MedlinePlus Genetics". medlineplus.gov. Retrieved 2020-11-12.

nih.gov

rarediseases.info.nih.gov

"SCARF syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Archived from the original on 28 June 2019. Retrieved 28 June 2019.
"SCARF syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Retrieved 2020-11-11.

pubmed.ncbi.nlm.nih.gov

Rahimpour, Masoume; Sohrabi, Mohammad bager; Kalhor, Sulmaz; Khosravi, Hossein ali; Zolfaghari, Poone; Yahyaei, Elahe (2014-03-16). "A rare case report: SCARF syndrome". Clinical Case Reports. 2 (3): 74–76. doi:10.1002/ccr3.61. ISSN 2050-0904. PMC 4184596. PMID 25356252.
Koppe, Roswitha; Kaplan, Paige; Hunter, Alasdair; MacMurray, Brock (1989). "Ambiguous genitalia associated with skeletal abnormalities, cutis laxa, craniostenosis, psychomotor retardation, and facial abnormalities (SCARF syndrome)". American Journal of Medical Genetics. 34 (3): 305–312. doi:10.1002/ajmg.1320340302. ISSN 1096-8628. PMID 2596519.

ncbi.nlm.nih.gov

Rahimpour, Masoume; Sohrabi, Mohammad bager; Kalhor, Sulmaz; Khosravi, Hossein ali; Zolfaghari, Poone; Yahyaei, Elahe (2014-03-16). "A rare case report: SCARF syndrome". Clinical Case Reports. 2 (3): 74–76. doi:10.1002/ccr3.61. ISSN 2050-0904. PMC 4184596. PMID 25356252.

omim.org

"OMIM Clinical Synopsis – 312830 – SCARF SYNDROME". omim.org. Retrieved 2020-11-11.

orpha.net

"Orphanet: SCARF syndrome". www.orpha.net. Retrieved 2020-11-12.
Mathijssen, Irene. "Genetic causes of craniofacial anomalies" (PDF).
Mathijssen, Irene. "Disturbed breathing in craniofacial disorders" (PDF).
"Orphanet: An Open label, Sequential, Ascending, Repeated Dose finding Study of Sarilumab, Administered with Subcutaneous SC Injection, in Children and Adolescents, Aged 2 to 17 Years, with Polyarticular course Juvenile Idiopathic Arthritis pcJIA Followed by an Extension Phase GB". www.orpha.net. Archived from the original on 2021-08-15. Retrieved 2020-11-12.

web.archive.org

"SCARF syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Archived from the original on 28 June 2019. Retrieved 28 June 2019.
"Orphanet: An Open label, Sequential, Ascending, Repeated Dose finding Study of Sarilumab, Administered with Subcutaneous SC Injection, in Children and Adolescents, Aged 2 to 17 Years, with Polyarticular course Juvenile Idiopathic Arthritis pcJIA Followed by an Extension Phase GB". www.orpha.net. Archived from the original on 2021-08-15. Retrieved 2020-11-12.

wiley.com

onlinelibrary.wiley.com

Koppe, Roswitha; Kaplan, Paige; Hunter, Alasdair; MacMurray, Brock (1989). "Ambiguous genitalia associated with skeletal abnormalities, cutis laxa, craniostenosis, psychomotor retardation, and facial abnormalities (SCARF syndrome)". American Journal of Medical Genetics. 34 (3): 305–312. doi:10.1002/ajmg.1320340302. ISSN 1096-8628. PMID 2596519.

worldcat.org

search.worldcat.org

Rahimpour, Masoume; Sohrabi, Mohammad bager; Kalhor, Sulmaz; Khosravi, Hossein ali; Zolfaghari, Poone; Yahyaei, Elahe (2014-03-16). "A rare case report: SCARF syndrome". Clinical Case Reports. 2 (3): 74–76. doi:10.1002/ccr3.61. ISSN 2050-0904. PMC 4184596. PMID 25356252.
Koppe, Roswitha; Kaplan, Paige; Hunter, Alasdair; MacMurray, Brock (1989). "Ambiguous genitalia associated with skeletal abnormalities, cutis laxa, craniostenosis, psychomotor retardation, and facial abnormalities (SCARF syndrome)". American Journal of Medical Genetics. 34 (3): 305–312. doi:10.1002/ajmg.1320340302. ISSN 1096-8628. PMID 2596519.