Cantú syndrome (English Wikipedia)

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

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Kirk, Edwin P.; Scurr, Ingrid; van Haaften, Gijs; van Haelst, Mieke M.; Nichols, Colin G.; Williams, Maggie; Smithson, Sarah F.; Grange, Dorothy K. (2017-04-01). "Clinical utility gene card for: Cantú syndrome". European Journal of Human Genetics. 25 (4): 512. doi:10.1038/ejhg.2016.185. ISSN 1018-4813. PMC 5386410. PMID 28051078.
Engels H, Bosse K, Ehrbrecht A, et al. (August 2002). "Further case of Cantú syndrome: exclusion of cryptic subtelomeric chromosome aberrations". Am. J. Med. Genet. 111 (2): 205–9. doi:10.1002/ajmg.10560. PMID 12210352.
Nichols, Colin G.; Singh, Gautam K.; Grange, Dorothy K. (2013-03-29). "KATP channels and cardiovascular disease: Suddenly a syndrome". Circulation Research. 112 (7): 1059–1072. doi:10.1161/CIRCRESAHA.112.300514. ISSN 0009-7330. PMC 3660033. PMID 23538276.

Kirk, Edwin P.; Scurr, Ingrid; van Haaften, Gijs; van Haelst, Mieke M.; Nichols, Colin G.; Williams, Maggie; Smithson, Sarah F.; Grange, Dorothy K. (2017-04-01). "Clinical utility gene card for: Cantú syndrome". European Journal of Human Genetics. 25 (4): 512. doi:10.1038/ejhg.2016.185. ISSN 1018-4813. PMC 5386410. PMID 28051078.
Grange, Dorothy K.; Nichols, Colin G.; Singh, Gautam K. (1993-01-01). "Cantú Syndrome and Related Disorders". In Pagon, Roberta A.; Adam, Margaret P.; Ardinger, Holly H.; Wallace, Stephanie E.; Amemiya, Anne; Bean, Lora J.H.; Bird, Thomas D.; Ledbetter, Nikki; Mefford, Heather C. (eds.). GeneReviews. Seattle (WA): University of Washington, Seattle. PMID 25275207. Archived from the original on 2020-08-13. Retrieved 2017-08-30.Initial posting 2014
Nichols, Colin G.; Singh, Gautam K.; Grange, Dorothy K. (2013-03-29). "KATP channels and cardiovascular disease: Suddenly a syndrome". Circulation Research. 112 (7): 1059–1072. doi:10.1161/CIRCRESAHA.112.300514. ISSN 0009-7330. PMC 3660033. PMID 23538276.
"Hypertrichotic osteochondrodysplasia - Conditions - GTR - NCBI". www.ncbi.nlm.nih.gov. Archived from the original on 2018-05-27. Retrieved 2017-04-01.

Kirk, Edwin P.; Scurr, Ingrid; van Haaften, Gijs; van Haelst, Mieke M.; Nichols, Colin G.; Williams, Maggie; Smithson, Sarah F.; Grange, Dorothy K. (2017-04-01). "Clinical utility gene card for: Cantú syndrome". European Journal of Human Genetics. 25 (4): 512. doi:10.1038/ejhg.2016.185. ISSN 1018-4813. PMC 5386410. PMID 28051078.
Grange, Dorothy K.; Nichols, Colin G.; Singh, Gautam K. (1993-01-01). "Cantú Syndrome and Related Disorders". In Pagon, Roberta A.; Adam, Margaret P.; Ardinger, Holly H.; Wallace, Stephanie E.; Amemiya, Anne; Bean, Lora J.H.; Bird, Thomas D.; Ledbetter, Nikki; Mefford, Heather C. (eds.). GeneReviews. Seattle (WA): University of Washington, Seattle. PMID 25275207. Archived from the original on 2020-08-13. Retrieved 2017-08-30.Initial posting 2014
Engels H, Bosse K, Ehrbrecht A, et al. (August 2002). "Further case of Cantú syndrome: exclusion of cryptic subtelomeric chromosome aberrations". Am. J. Med. Genet. 111 (2): 205–9. doi:10.1002/ajmg.10560. PMID 12210352.
Nichols, Colin G.; Singh, Gautam K.; Grange, Dorothy K. (2013-03-29). "KATP channels and cardiovascular disease: Suddenly a syndrome". Circulation Research. 112 (7): 1059–1072. doi:10.1161/CIRCRESAHA.112.300514. ISSN 0009-7330. PMC 3660033. PMID 23538276.

Reference, Genetics Home. "ABCC9 gene". Genetics Home Reference. Archived from the original on 29 March 2019. Retrieved 23 March 2017.
Reference, Genetics Home. "Cantú syndrome". Genetics Home Reference. Archived from the original on 2019-03-29. Retrieved 2017-03-23.

Pubchem. "Prostaglandin E2 | C20H32O5 - PubChem". pubchem.ncbi.nlm.nih.gov. Archived from the original on 2019-03-30. Retrieved 2017-04-01.

"OMIM Entry - # 239850 - CANTU SYNDROME". omim.org. Archived from the original on 2019-03-30. Retrieved 2017-04-01.

"OMIM Entry - # 239850 - CANTU SYNDROME". omim.org. Archived from the original on 2019-03-30. Retrieved 2017-04-01.
"Cantu syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Archived from the original on 2019-03-29. Retrieved 2017-03-31.
Reference, Genetics Home. "ABCC9 gene". Genetics Home Reference. Archived from the original on 29 March 2019. Retrieved 23 March 2017.
Grange, Dorothy K.; Nichols, Colin G.; Singh, Gautam K. (1993-01-01). "Cantú Syndrome and Related Disorders". In Pagon, Roberta A.; Adam, Margaret P.; Ardinger, Holly H.; Wallace, Stephanie E.; Amemiya, Anne; Bean, Lora J.H.; Bird, Thomas D.; Ledbetter, Nikki; Mefford, Heather C. (eds.). GeneReviews. Seattle (WA): University of Washington, Seattle. PMID 25275207. Archived from the original on 2020-08-13. Retrieved 2017-08-30.Initial posting 2014
Reference, Genetics Home. "Cantú syndrome". Genetics Home Reference. Archived from the original on 2019-03-29. Retrieved 2017-03-23.
Pubchem. "Prostaglandin E2 | C20H32O5 - PubChem". pubchem.ncbi.nlm.nih.gov. Archived from the original on 2019-03-30. Retrieved 2017-04-01.
"Hypertrichotic osteochondrodysplasia - Conditions - GTR - NCBI". www.ncbi.nlm.nih.gov. Archived from the original on 2018-05-27. Retrieved 2017-04-01.

Kirk, Edwin P.; Scurr, Ingrid; van Haaften, Gijs; van Haelst, Mieke M.; Nichols, Colin G.; Williams, Maggie; Smithson, Sarah F.; Grange, Dorothy K. (2017-04-01). "Clinical utility gene card for: Cantú syndrome". European Journal of Human Genetics. 25 (4): 512. doi:10.1038/ejhg.2016.185. ISSN 1018-4813. PMC 5386410. PMID 28051078.
Nichols, Colin G.; Singh, Gautam K.; Grange, Dorothy K. (2013-03-29). "KATP channels and cardiovascular disease: Suddenly a syndrome". Circulation Research. 112 (7): 1059–1072. doi:10.1161/CIRCRESAHA.112.300514. ISSN 0009-7330. PMC 3660033. PMID 23538276.