Piebaldism (English Wikipedia)

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

refsWebsite

Global rank English rank

4^th place

4^th place

2^nd place

2^nd place

1web.archive.org

1^st place

1^st place

1medlineplus.gov

1,581^st place

1,299^th place

18^th place

17^th place

26^th place

20^th place

1semanticscholar.org

11^th place

8^th place

1etymonline.com

287^th place

321^st place

1books.google.com

3^rd place

3^rd place

books.google.com

Skeat, Walter W. (1882). The Concise Dictionary of English Etymology. Hertfordshire: Clarendon Press. p. 442.

doi.org

Giebel, L. B.; Spritz, R. A. (1991). "Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism". Proceedings of the National Academy of Sciences. 88 (19): 8696–9. Bibcode:1991PNAS...88.8696G. doi:10.1073/pnas.88.19.8696. JSTOR 2358007. PMC 52576. PMID 1717985.
Sánchez-Martín M, Pérez-Losada J, Rodríguez-García A, et al. (October 2003). "Deletion of the SLUG (SNAI2) gene results in human piebaldism". Am. J. Med. Genet. A. 122A (2): 125–32. doi:10.1002/ajmg.a.20345. PMID 12955764. S2CID 33811699.
Spritz, RA (1997). "Piebaldism, Waardenburg syndrome, and related disorders of melanocyte development". Seminars in Cutaneous Medicine and Surgery. 16 (1): 15–23. doi:10.1016/s1085-5629(97)80031-4. PMID 9125761.

etymonline.com

Harper, Douglas. "Piebald". Online Etymology Dictionary.

harvard.edu

ui.adsabs.harvard.edu

Giebel, L. B.; Spritz, R. A. (1991). "Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism". Proceedings of the National Academy of Sciences. 88 (19): 8696–9. Bibcode:1991PNAS...88.8696G. doi:10.1073/pnas.88.19.8696. JSTOR 2358007. PMC 52576. PMID 1717985.

jstor.org

Giebel, L. B.; Spritz, R. A. (1991). "Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism". Proceedings of the National Academy of Sciences. 88 (19): 8696–9. Bibcode:1991PNAS...88.8696G. doi:10.1073/pnas.88.19.8696. JSTOR 2358007. PMC 52576. PMID 1717985.

medlineplus.gov

MedlinePlus Encyclopedia: Autosomal dominant

nih.gov

pubmed.ncbi.nlm.nih.gov

Giebel, L. B.; Spritz, R. A. (1991). "Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism". Proceedings of the National Academy of Sciences. 88 (19): 8696–9. Bibcode:1991PNAS...88.8696G. doi:10.1073/pnas.88.19.8696. JSTOR 2358007. PMC 52576. PMID 1717985.
Sánchez-Martín M, Pérez-Losada J, Rodríguez-García A, et al. (October 2003). "Deletion of the SLUG (SNAI2) gene results in human piebaldism". Am. J. Med. Genet. A. 122A (2): 125–32. doi:10.1002/ajmg.a.20345. PMID 12955764. S2CID 33811699.
Spritz, RA (1997). "Piebaldism, Waardenburg syndrome, and related disorders of melanocyte development". Seminars in Cutaneous Medicine and Surgery. 16 (1): 15–23. doi:10.1016/s1085-5629(97)80031-4. PMID 9125761.

ncbi.nlm.nih.gov

"Partial Albinism". Retrieved Jan 1, 2024.
Giebel, L. B.; Spritz, R. A. (1991). "Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism". Proceedings of the National Academy of Sciences. 88 (19): 8696–9. Bibcode:1991PNAS...88.8696G. doi:10.1073/pnas.88.19.8696. JSTOR 2358007. PMC 52576. PMID 1717985.

rarediseases.info.nih.gov

"Piebaldism | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Archived from the original on 16 April 2019. Retrieved 16 April 2019.

semanticscholar.org

api.semanticscholar.org

Sánchez-Martín M, Pérez-Losada J, Rodríguez-García A, et al. (October 2003). "Deletion of the SLUG (SNAI2) gene results in human piebaldism". Am. J. Med. Genet. A. 122A (2): 125–32. doi:10.1002/ajmg.a.20345. PMID 12955764. S2CID 33811699.

web.archive.org

"Piebaldism | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Archived from the original on 16 April 2019. Retrieved 16 April 2019.