Sindrom Char (Indonesian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Sindrom Char" in Indonesian language version.

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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 (dalam bahasa Inggris). 121 (9): 2779–2788. 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.
Satoda, Masahiko; Zhao, Feng; Diaz, George A.; Burn, John; Goodship, Judith; Davidson, H. Rosemarie; Pierpont, Mary Ella M.; Gelb, Bruce D. (2000-05). "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.
Zannolli, R.; Mostardini, R.; Matera, M.; Pucci, L.; Gelb, B.D.; Morgese, G. (2000). <201::aid-ajmg3>3.0.co;2-w "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.

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.
Satoda, Masahiko; Zhao, Feng; Diaz, George A.; Burn, John; Goodship, Judith; Davidson, H. Rosemarie; Pierpont, Mary Ella M.; Gelb, Bruce D. (2000-05). "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.
Zannolli, R.; Mostardini, R.; Matera, M.; Pucci, L.; Gelb, B.D.; Morgese, G. (2000). <201::aid-ajmg3>3.0.co;2-w "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.

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 (dalam bahasa Inggris). 121 (9): 2779–2788. ISSN 0950-1991. PMID 7555706.

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 (dalam bahasa Inggris). 121 (9): 2779–2788. 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.
Satoda, Masahiko; Zhao, Feng; Diaz, George A.; Burn, John; Goodship, Judith; Davidson, H. Rosemarie; Pierpont, Mary Ella M.; Gelb, Bruce D. (2000-05). "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.
Zannolli, R.; Mostardini, R.; Matera, M.; Pucci, L.; Gelb, B.D.; Morgese, G. (2000). <201::aid-ajmg3>3.0.co;2-w "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.