АБЦД синдром (Serbian Wikipedia)

Analysis of information sources in references of the Wikipedia article "АБЦД синдром" in Serbian language version.

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14nih.gov

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8doi.org

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archive.org

Waardenburg, P. J. (септембар 1951). „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”. American Journal of Human Genetics. 3 (3): 195—253. PMC 1716407 . PMID 14902764.
Waardenburg, P. J. (септембар 1951). „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”. American Journal of Human Genetics. 3 (3): 195—253. PMC 1716407 . PMID 14902764.
Waardenburg, P. J. (септембар 1951). „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”. American Journal of Human Genetics. 3 (3): 195—253. PMC 1716407 . PMID 14902764.
Waardenburg, P. J. (септембар 1951). „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”. American Journal of Human Genetics. 3 (3): 195—253. PMC 1716407 . PMID 14902764.
Waardenburg, P. J. (септембар 1951). „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”. American Journal of Human Genetics. 3 (3): 195—253. PMC 1716407 . PMID 14902764.
Waardenburg, P. J. (септембар 1951). „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”. American Journal of Human Genetics. 3 (3): 195—253. PMC 1716407 . PMID 14902764.
Sato-Jin, Kayo; et al. (април 2008). „Epistatic connections between microphthalmia-associated transcription factor and endothelin signaling in Waardenburg syndrome and other pigmentary disorders”. FASEB Journal. 22 (4): 1155—1168. PMID 18039926. doi:10.1096/fj.07-9080com.

doi.org

„Autosomal-recessive neural crest syndrome with albinism, black lock, cell migration disorder of the neurocytes of the gut, and deafness: ABCD syndrome”. Am J Med Genet. 56 (3): 322—6. 1995. PMID 7778600. doi:10.1002/ajmg.1320560322.
Verheij, Joke B.G.M.; Jurgen Kunze; Jan Osinga; Anthonie J. van Essen; Robert M. W. Hofstra (јануар 2002). „ABCD Syndrome is Caused by a Homozygous Mutation in the EDNRB Gene”. American Journal of Medical Genetics. 108 (3): 223—225. PMID 11891690. doi:10.1002/ajmg.10172.
Verheij, Joke B.G.M.; Jurgen Kunze; Jan Osinga; Anthonie J. van Essen; Robert M. W. Hofstra (јануар 2002). „ABCD Syndrome is Caused by a Homozygous Mutation in the EDNRB Gene”. American Journal of Medical Genetics. 108 (3): 223—225. PMID 11891690. doi:10.1002/ajmg.10172.
„Autosomal-recessive neural crest syndrome with albinism, black lock, cell migration disorder of the neurocytes of the gut, and deafness: ABCD syndrome”. Am J Med Genet. 56 (3): 322—6. 1995. PMID 7778600. doi:10.1002/ajmg.1320560322.
Verheij, Joke B.G.M.; Jurgen Kunze; Jan Osinga; Anthonie J. van Essen; Robert M. W. Hofstra (јануар 2002). „ABCD Syndrome is Caused by a Homozygous Mutation in the EDNRB Gene”. American Journal of Medical Genetics. 108 (3): 223—225. PMID 11891690. doi:10.1002/ajmg.10172.
Verheij, Joke B.G.M.; Jurgen Kunze; Jan Osinga; Anthonie J. van Essen; Robert M. W. Hofstra (јануар 2002). „ABCD Syndrome is Caused by a Homozygous Mutation in the EDNRB Gene”. American Journal of Medical Genetics. 108 (3): 223—225. PMID 11891690. doi:10.1002/ajmg.10172.
Sato-Jin, Kayo; et al. (април 2008). „Epistatic connections between microphthalmia-associated transcription factor and endothelin signaling in Waardenburg syndrome and other pigmentary disorders”. FASEB Journal. 22 (4): 1155—1168. PMID 18039926. doi:10.1096/fj.07-9080com.
Kujat, Annegret; et al. (март 2007). „Prenatal Diagnosis and Genetic Counseling in a Case of Spina Bifida in a Family with Waardenburg Syndrome Type I”. Fetal Diagnosis and Therapy. 22 (2): 155—158. PMID 17139175. doi:10.1159/000097117.

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”. Am J Med Genet. 56 (3): 322—6. 1995. PMID 7778600. doi:10.1002/ajmg.1320560322.
Verheij, Joke B.G.M.; Jurgen Kunze; Jan Osinga; Anthonie J. van Essen; Robert M. W. Hofstra (јануар 2002). „ABCD Syndrome is Caused by a Homozygous Mutation in the EDNRB Gene”. American Journal of Medical Genetics. 108 (3): 223—225. PMID 11891690. doi:10.1002/ajmg.10172.
Waardenburg, P. J. (септембар 1951). „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”. American Journal of Human Genetics. 3 (3): 195—253. PMC 1716407 . PMID 14902764.
Waardenburg, P. J. (септембар 1951). „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”. American Journal of Human Genetics. 3 (3): 195—253. PMC 1716407 . PMID 14902764.
Waardenburg, P. J. (септембар 1951). „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”. American Journal of Human Genetics. 3 (3): 195—253. PMC 1716407 . PMID 14902764.
Waardenburg, P. J. (септембар 1951). „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”. American Journal of Human Genetics. 3 (3): 195—253. PMC 1716407 . PMID 14902764.
Waardenburg, P. J. (септембар 1951). „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”. American Journal of Human Genetics. 3 (3): 195—253. PMC 1716407 . PMID 14902764.
Waardenburg, P. J. (септембар 1951). „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”. American Journal of Human Genetics. 3 (3): 195—253. PMC 1716407 . PMID 14902764.
Verheij, Joke B.G.M.; Jurgen Kunze; Jan Osinga; Anthonie J. van Essen; Robert M. W. Hofstra (јануар 2002). „ABCD Syndrome is Caused by a Homozygous Mutation in the EDNRB Gene”. American Journal of Medical Genetics. 108 (3): 223—225. PMID 11891690. doi:10.1002/ajmg.10172.
„Autosomal-recessive neural crest syndrome with albinism, black lock, cell migration disorder of the neurocytes of the gut, and deafness: ABCD syndrome”. Am J Med Genet. 56 (3): 322—6. 1995. PMID 7778600. doi:10.1002/ajmg.1320560322.
Verheij, Joke B.G.M.; Jurgen Kunze; Jan Osinga; Anthonie J. van Essen; Robert M. W. Hofstra (јануар 2002). „ABCD Syndrome is Caused by a Homozygous Mutation in the EDNRB Gene”. American Journal of Medical Genetics. 108 (3): 223—225. PMID 11891690. doi:10.1002/ajmg.10172.
Verheij, Joke B.G.M.; Jurgen Kunze; Jan Osinga; Anthonie J. van Essen; Robert M. W. Hofstra (јануар 2002). „ABCD Syndrome is Caused by a Homozygous Mutation in the EDNRB Gene”. American Journal of Medical Genetics. 108 (3): 223—225. PMID 11891690. doi:10.1002/ajmg.10172.
Sato-Jin, Kayo; et al. (април 2008). „Epistatic connections between microphthalmia-associated transcription factor and endothelin signaling in Waardenburg syndrome and other pigmentary disorders”. FASEB Journal. 22 (4): 1155—1168. PMID 18039926. doi:10.1096/fj.07-9080com.
Kujat, Annegret; et al. (март 2007). „Prenatal Diagnosis and Genetic Counseling in a Case of Spina Bifida in a Family with Waardenburg Syndrome Type I”. Fetal Diagnosis and Therapy. 22 (2): 155—158. PMID 17139175. doi:10.1159/000097117.