KBG-Syndrom (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "KBG-Syndrom" in German language version.

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F. Brancati, A. Sarkozy, B. Dallapiccola: KBG syndrome. In: Orphanet Journal of Rare Diseases. Band 1, 2006, S. 50, ISSN 1750-1172. doi:10.1186/1750-1172-1-50. PMID 17163996. PMC 1764006 (freier Volltext). (Review-Artikel im Open Access).
M. Tekin, A. Kavaz u. a.: The KBG syndrome: confirmation of autosomal dominant inheritance and further delineation of the phenotype. In: American journal of medical genetics. Part A. Band 130A, Nummer 3, Oktober 2004, S. 284–287, ISSN 1552-4825. doi:10.1002/ajmg.a.30291. PMID 15378538. (Review).

R. Witkowski, O. Prokop u. a.: Lexikon der Syndrome und Fehlbildungen. Springer, 2003, ISBN 3-540-44305-3, S. 530. eingeschränkte Vorschau in der Google-Buchsuche

F. Brancati, A. Sarkozy, B. Dallapiccola: KBG syndrome. In: Orphanet Journal of Rare Diseases. Band 1, 2006, S. 50, ISSN 1750-1172. doi:10.1186/1750-1172-1-50. PMID 17163996. PMC 1764006 (freier Volltext). (Review-Artikel im Open Access).
M. Tekin, A. Kavaz u. a.: The KBG syndrome: confirmation of autosomal dominant inheritance and further delineation of the phenotype. In: American journal of medical genetics. Part A. Band 130A, Nummer 3, Oktober 2004, S. 284–287, ISSN 1552-4825. doi:10.1002/ajmg.a.30291. PMID 15378538. (Review).
J. Herrmann, P. D. Pallister u. a.: The KBG syndrome-a syndrome of short stature, characteristic facies, mental retardation, macrodontia and skeletal anomalies. In: Birth defects original article series. Band 11, Nummer 5, 1975, S. 7–18, ISSN 0547-6844. PMID 1218237.

F. Brancati, A. Sarkozy, B. Dallapiccola: KBG syndrome. In: Orphanet Journal of Rare Diseases. Band 1, 2006, S. 50, ISSN 1750-1172. doi:10.1186/1750-1172-1-50. PMID 17163996. PMC 1764006 (freier Volltext). (Review-Artikel im Open Access).
M. Tekin, A. Kavaz u. a.: The KBG syndrome: confirmation of autosomal dominant inheritance and further delineation of the phenotype. In: American journal of medical genetics. Part A. Band 130A, Nummer 3, Oktober 2004, S. 284–287, ISSN 1552-4825. doi:10.1002/ajmg.a.30291. PMID 15378538. (Review).
J. Herrmann, P. D. Pallister u. a.: The KBG syndrome-a syndrome of short stature, characteristic facies, mental retardation, macrodontia and skeletal anomalies. In: Birth defects original article series. Band 11, Nummer 5, 1975, S. 7–18, ISSN 0547-6844. PMID 1218237.