Вулф-Хершонов синдром (Serbian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Вулф-Хершонов синдром" in Serbian language version.

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10nih.gov

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9doi.org

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1web.archive.org

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1orpha.net

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1archive.org

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archive.org

„Antibody deficiency in Wolf-Hirschhorn syndrome”. The Journal of Pediatrics. 133 (1): 141—3. јул 1998. PMID 9672528. doi:10.1016/S0022-3476(98)70194-5.

doi.org

„Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn syndrome”. Cytogenetics and Cell Genetics. 91 (1–4): 81—4. 2000. PMID 11173835. doi:10.1159/000056823.
„Wolf-Hirschhorn syndrome (WHS) - literature review on the features of the syndrome”. Adv Clin Exp Med. 23 (3): 485—9. 2014. PMID 24979523. doi:10.17219/acem/24111 .
„Antibody deficiency in Wolf-Hirschhorn syndrome”. The Journal of Pediatrics. 133 (1): 141—3. јул 1998. PMID 9672528. doi:10.1016/S0022-3476(98)70194-5.
„First known microdeletion within the Wolf-Hirschhorn syndrome critical region refines genotype-phenotype correlation”. American Journal of Medical Genetics. 99 (4): 338—42. април 2001. PMID 11252005. doi:10.1002/ajmg.1203.
„Wolf-Hirschhorn syndrome (WHS) - literature review on the features of the syndrome”. Adv Clin Exp Med. 23 (3): 485—9. 2014. PMID 24979523. doi:10.17219/acem/24111 .
„Wolf-Hirschhorn syndrome (WHS) - literature review on the features of the syndrome”. Adv Clin Exp Med. 23 (3): 485—9. 2014. PMID 24979523. doi:10.17219/acem/24111 .
„Wolf-Hirschhorn syndrome (WHS) - literature review on the features of the syndrome”. Adv Clin Exp Med. 23 (3): 485—9. 2014. PMID 24979523. doi:10.17219/acem/24111 .
„Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion”. Humangenetik. 1 (5): 479—82. 1961. PMID 5895684. doi:10.1007/bf00279124.
„Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion”. Humangenetik. 1 (5): 479—82. 1961. PMID 5895684. doi:10.1007/bf00279124.

nih.gov

ncbi.nlm.nih.gov

„Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn syndrome”. Cytogenetics and Cell Genetics. 91 (1–4): 81—4. 2000. PMID 11173835. doi:10.1159/000056823.
„Wolf-Hirschhorn syndrome (WHS) - literature review on the features of the syndrome”. Adv Clin Exp Med. 23 (3): 485—9. 2014. PMID 24979523. doi:10.17219/acem/24111 .
„Antibody deficiency in Wolf-Hirschhorn syndrome”. The Journal of Pediatrics. 133 (1): 141—3. јул 1998. PMID 9672528. doi:10.1016/S0022-3476(98)70194-5.
„First known microdeletion within the Wolf-Hirschhorn syndrome critical region refines genotype-phenotype correlation”. American Journal of Medical Genetics. 99 (4): 338—42. април 2001. PMID 11252005. doi:10.1002/ajmg.1203.
„Wolf-Hirschhorn syndrome (WHS) - literature review on the features of the syndrome”. Adv Clin Exp Med. 23 (3): 485—9. 2014. PMID 24979523. doi:10.17219/acem/24111 .
„Wolf-Hirschhorn syndrome (WHS) - literature review on the features of the syndrome”. Adv Clin Exp Med. 23 (3): 485—9. 2014. PMID 24979523. doi:10.17219/acem/24111 .
„Wolf-Hirschhorn syndrome (WHS) - literature review on the features of the syndrome”. Adv Clin Exp Med. 23 (3): 485—9. 2014. PMID 24979523. doi:10.17219/acem/24111 .
„Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion”. Humangenetik. 1 (5): 479—82. 1961. PMID 5895684. doi:10.1007/bf00279124.
„Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion”. Humangenetik. 1 (5): 479—82. 1961. PMID 5895684. doi:10.1007/bf00279124.
„[Deficiency on the short arms of a chromosome No. 4]”. Humangenetik (на језику: German). 1 (5): 397—413. 1965. PMID 5868696.

orpha.net

„Wolf-Hirschhorn syndrome” (PDF). Orphanet encyclopedia. септембар 2003. Архивирано из оригинала (PDF) 09. 03. 2021. г. Приступљено 03. 12. 2022.

web.archive.org

„Wolf-Hirschhorn syndrome” (PDF). Orphanet encyclopedia. септембар 2003. Архивирано из оригинала (PDF) 09. 03. 2021. г. Приступљено 03. 12. 2022.