Sindrome ABCD (Italian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Sindrome ABCD" in Italian language version.

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doi.org

dx.doi.org

Autosomal-recessive neural crest syndrome with albinism, black lock, cell migration disorder of the neurocytes of the gut, and deafness: ABCD syndrome, in Am J Med Genet, vol. 56, n. 3, 1995, pp. 322–6, DOI:10.1002/ajmg.1320560322, PMID 7778600.
Verheij, Joke B.G.M., Jurgen Kunze e Jan Osinga, ABCD Syndrome is Caused by a Homozygous Mutation in the EDNRB Gene, in American Journal of Medical Genetics, vol. 108, n. 3, January 2002, pp. 223–225, DOI:10.1002/ajmg.10172, PMID 11891690.^{[collegamento interrotto]}
Kujat, Annegret, Prenatal Diagnosis and Genetic Counseling in a Case of Spina Bifida in a Family with Waardenburg Syndrome Type I, in Fetal Diagnosis and Therapy, vol. 22, n. 2, March 2007, pp. 155–158, DOI:10.1159/000097117, PMID 17139175.

nih.gov

ncbi.nlm.nih.gov

Autosomal-recessive neural crest syndrome with albinism, black lock, cell migration disorder of the neurocytes of the gut, and deafness: ABCD syndrome, in Am J Med Genet, vol. 56, n. 3, 1995, pp. 322–6, DOI:10.1002/ajmg.1320560322, PMID 7778600.
Verheij, Joke B.G.M., Jurgen Kunze e Jan Osinga, ABCD Syndrome is Caused by a Homozygous Mutation in the EDNRB Gene, in American Journal of Medical Genetics, vol. 108, n. 3, January 2002, pp. 223–225, DOI:10.1002/ajmg.10172, PMID 11891690.^{[collegamento interrotto]}
Kujat, Annegret, Prenatal Diagnosis and Genetic Counseling in a Case of Spina Bifida in a Family with Waardenburg Syndrome Type I, in Fetal Diagnosis and Therapy, vol. 22, n. 2, March 2007, pp. 155–158, DOI:10.1159/000097117, PMID 17139175.
P. J. Waardenburg, A new syndrome combining developmental anomalies of the eyelids, eyebrows and noseroot with pigmentary anomalies of the iris and head hair and with congenital deafness, in American Journal of Human Genetics, vol. 3, n. 3, September 1951, pp. 195–253, PMID 14902764.

oadoi.org

Autosomal-recessive neural crest syndrome with albinism, black lock, cell migration disorder of the neurocytes of the gut, and deafness: ABCD syndrome, in Am J Med Genet, vol. 56, n. 3, 1995, pp. 322–6, DOI:10.1002/ajmg.1320560322, PMID 7778600.
Kujat, Annegret, Prenatal Diagnosis and Genetic Counseling in a Case of Spina Bifida in a Family with Waardenburg Syndrome Type I, in Fetal Diagnosis and Therapy, vol. 22, n. 2, March 2007, pp. 155–158, DOI:10.1159/000097117, PMID 17139175.

wiley.com

www3.interscience.wiley.com

Verheij, Joke B.G.M., Jurgen Kunze e Jan Osinga, ABCD Syndrome is Caused by a Homozygous Mutation in the EDNRB Gene, in American Journal of Medical Genetics, vol. 108, n. 3, January 2002, pp. 223–225, DOI:10.1002/ajmg.10172, PMID 11891690.^{[collegamento interrotto]}