Char syndrome (English Wikipedia)

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

refsWebsite

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7nih.gov

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5worldcat.org

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5doi.org

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1orpha.net

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1biologists.org

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1semanticscholar.org

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1ahajournals.org

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ahajournals.org

Satoda, Masahiko; Pierpont, Mary Ella M.; Diaz, George A.; Bornemeier, Renee A.; Gelb, Bruce D. (1999). "Char Syndrome, an Inherited Disorder with Patent Ductus Arteriosus, Maps to Chromosome 6p12-p21". Circulation. 99 (23): 3036–3042. doi:10.1161/01.CIR.99.23.3036. PMID 10368122.

biologists.org

dev.biologists.org

Buettner, R.; Schule, R.; Hofstadter, F.; Sinowatz, F.; Amselgruber, W.; Bauer, R.; Pscherer, A.; Imhof, A.; Moser, M. (1995-09-01). "Cloning and characterization of a second AP-2 transcription factor: AP-2 beta". Development. 121 (9): 2779–2788. doi:10.1242/dev.121.9.2779. ISSN 0950-1991. PMID 7555706.

doi.org

Buettner, R.; Schule, R.; Hofstadter, F.; Sinowatz, F.; Amselgruber, W.; Bauer, R.; Pscherer, A.; Imhof, A.; Moser, M. (1995-09-01). "Cloning and characterization of a second AP-2 transcription factor: AP-2 beta". Development. 121 (9): 2779–2788. doi:10.1242/dev.121.9.2779. ISSN 0950-1991. PMID 7555706.
Satoda, Masahiko; Pierpont, Mary Ella M.; Diaz, George A.; Bornemeier, Renee A.; Gelb, Bruce D. (1999-06-15). "Char Syndrome, an Inherited Disorder With Patent Ductus Arteriosus, Maps to Chromosome 6p12-p21". Circulation. 99 (23): 3036–3042. doi:10.1161/01.cir.99.23.3036. ISSN 0009-7322. PMID 10368122.
Satoda, Masahiko; Zhao, Feng; Diaz, George A.; Burn, John; Goodship, Judith; Davidson, H. Rosemarie; Pierpont, Mary Ella M.; Gelb, Bruce D. (May 2000). "Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus". Nature Genetics. 25 (1): 42–46. doi:10.1038/75578. ISSN 1061-4036. PMID 10802654. S2CID 37890243.
Zannolli, R.; Mostardini, R.; Matera, M.; Pucci, L.; Gelb, B.D.; Morgese, G. (2000). "Char syndrome: An additional family with polythelia, a new finding". American Journal of Medical Genetics. 95 (3): 201–203. doi:10.1002/1096-8628(20001127)95:3<201::aid-ajmg3>3.0.co;2-w. ISSN 0148-7299. PMID 11102923.
Satoda, Masahiko; Pierpont, Mary Ella M.; Diaz, George A.; Bornemeier, Renee A.; Gelb, Bruce D. (1999). "Char Syndrome, an Inherited Disorder with Patent Ductus Arteriosus, Maps to Chromosome 6p12-p21". Circulation. 99 (23): 3036–3042. doi:10.1161/01.CIR.99.23.3036. PMID 10368122.

nih.gov

pubmed.ncbi.nlm.nih.gov

Char, F. (1978). "Peculiar facies with short philtrum, duck-bill lips, ptosis and low-set ears--a new syndrome?". Birth Defects Original Article Series. 14 (6B): 303–305. ISSN 0547-6844. PMID 728571.
Buettner, R.; Schule, R.; Hofstadter, F.; Sinowatz, F.; Amselgruber, W.; Bauer, R.; Pscherer, A.; Imhof, A.; Moser, M. (1995-09-01). "Cloning and characterization of a second AP-2 transcription factor: AP-2 beta". Development. 121 (9): 2779–2788. doi:10.1242/dev.121.9.2779. ISSN 0950-1991. PMID 7555706.
Satoda, Masahiko; Pierpont, Mary Ella M.; Diaz, George A.; Bornemeier, Renee A.; Gelb, Bruce D. (1999-06-15). "Char Syndrome, an Inherited Disorder With Patent Ductus Arteriosus, Maps to Chromosome 6p12-p21". Circulation. 99 (23): 3036–3042. doi:10.1161/01.cir.99.23.3036. ISSN 0009-7322. PMID 10368122.
Satoda, Masahiko; Zhao, Feng; Diaz, George A.; Burn, John; Goodship, Judith; Davidson, H. Rosemarie; Pierpont, Mary Ella M.; Gelb, Bruce D. (May 2000). "Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus". Nature Genetics. 25 (1): 42–46. doi:10.1038/75578. ISSN 1061-4036. PMID 10802654. S2CID 37890243.
Zannolli, R.; Mostardini, R.; Matera, M.; Pucci, L.; Gelb, B.D.; Morgese, G. (2000). "Char syndrome: An additional family with polythelia, a new finding". American Journal of Medical Genetics. 95 (3): 201–203. doi:10.1002/1096-8628(20001127)95:3<201::aid-ajmg3>3.0.co;2-w. ISSN 0148-7299. PMID 11102923.
Satoda, Masahiko; Pierpont, Mary Ella M.; Diaz, George A.; Bornemeier, Renee A.; Gelb, Bruce D. (1999). "Char Syndrome, an Inherited Disorder with Patent Ductus Arteriosus, Maps to Chromosome 6p12-p21". Circulation. 99 (23): 3036–3042. doi:10.1161/01.CIR.99.23.3036. PMID 10368122.

rarediseases.info.nih.gov

"Char syndrome". rarediseases.info.nih.gov. Genetic and Rare Diseases Information Center, National Center for Advancing Translational Sciences. Retrieved 2019-04-15.

orpha.net

RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Char syndrome". www.orpha.net. Retrieved 27 October 2019.{{cite web}}: CS1 maint: numeric names: authors list (link)

semanticscholar.org

api.semanticscholar.org

Satoda, Masahiko; Zhao, Feng; Diaz, George A.; Burn, John; Goodship, Judith; Davidson, H. Rosemarie; Pierpont, Mary Ella M.; Gelb, Bruce D. (May 2000). "Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus". Nature Genetics. 25 (1): 42–46. doi:10.1038/75578. ISSN 1061-4036. PMID 10802654. S2CID 37890243.

worldcat.org

search.worldcat.org

Char, F. (1978). "Peculiar facies with short philtrum, duck-bill lips, ptosis and low-set ears--a new syndrome?". Birth Defects Original Article Series. 14 (6B): 303–305. ISSN 0547-6844. PMID 728571.
Buettner, R.; Schule, R.; Hofstadter, F.; Sinowatz, F.; Amselgruber, W.; Bauer, R.; Pscherer, A.; Imhof, A.; Moser, M. (1995-09-01). "Cloning and characterization of a second AP-2 transcription factor: AP-2 beta". Development. 121 (9): 2779–2788. doi:10.1242/dev.121.9.2779. ISSN 0950-1991. PMID 7555706.
Satoda, Masahiko; Pierpont, Mary Ella M.; Diaz, George A.; Bornemeier, Renee A.; Gelb, Bruce D. (1999-06-15). "Char Syndrome, an Inherited Disorder With Patent Ductus Arteriosus, Maps to Chromosome 6p12-p21". Circulation. 99 (23): 3036–3042. doi:10.1161/01.cir.99.23.3036. ISSN 0009-7322. PMID 10368122.
Satoda, Masahiko; Zhao, Feng; Diaz, George A.; Burn, John; Goodship, Judith; Davidson, H. Rosemarie; Pierpont, Mary Ella M.; Gelb, Bruce D. (May 2000). "Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus". Nature Genetics. 25 (1): 42–46. doi:10.1038/75578. ISSN 1061-4036. PMID 10802654. S2CID 37890243.
Zannolli, R.; Mostardini, R.; Matera, M.; Pucci, L.; Gelb, B.D.; Morgese, G. (2000). "Char syndrome: An additional family with polythelia, a new finding". American Journal of Medical Genetics. 95 (3): 201–203. doi:10.1002/1096-8628(20001127)95:3<201::aid-ajmg3>3.0.co;2-w. ISSN 0148-7299. PMID 11102923.