3M-Syndrom (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "3M-Syndrom" in German language version.

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M. Le Merrer, R. Brauner, P. Maroteaux: Dwarfism with gloomy face: a new syndrome with features of 3-M syndrome. In: Journal of Medical Genetics. Band 28, Nummer 3, März 1991, S. 186–191, doi:10.1136/jmg.28.3.186, PMID 2051454, PMC 1016803 (freier Volltext).
N. Maksimova, K. Hara, A. Miyashia et al.: Clinical, molecular and histopathological features of short stature syndrome with novel CUL7 mutation in Yakuts: new population isolate in Asia. In: Journal of Medical Genetics. Band 44, Nummer 12, Dezember 2007, S. 772–778, doi:10.1136/jmg.2007.051979, PMID 17675530, PMC 2652813 (freier Volltext).
A. G. Tsiotou, A. Malisiova, E. Kalliardou: Anaesthesia and orphan disease: the child with 3M syndrome. In: European journal of anaesthesiology. Band 29, Nummer 12, Dezember 2012, S. 598–600, ISSN 1365-2346. doi:10.1097/EJA.0b013e32835a9a6c. PMID 23080434.

M: Irving, M. Holder-Espinasse: Three M Syndrome. In: GeneReviews®
J. D. Miller, V. A. McKusick, P. Malvaux, S. Temtamy, C. Salinas: The 3-M syndrome: a heritable low birthweight dwarfism. In: Birth defects original article series. Band 11, Nummer 5, 1975, S. 39–47, ISSN 0547-6844. PMID 1218233.
M. Le Merrer, R. Brauner, P. Maroteaux: Dwarfism with gloomy face: a new syndrome with features of 3-M syndrome. In: Journal of Medical Genetics. Band 28, Nummer 3, März 1991, S. 186–191, doi:10.1136/jmg.28.3.186, PMID 2051454, PMC 1016803 (freier Volltext).
N. Maksimova, K. Hara, A. Miyashia et al.: Clinical, molecular and histopathological features of short stature syndrome with novel CUL7 mutation in Yakuts: new population isolate in Asia. In: Journal of Medical Genetics. Band 44, Nummer 12, Dezember 2007, S. 772–778, doi:10.1136/jmg.2007.051979, PMID 17675530, PMC 2652813 (freier Volltext).
F. Meo, V. Pinto, V. D’Addario: 3-M syndrome: a prenatal ultrasonographic diagnosis. In: Prenatal diagnosis. Band 20, Nummer 11, November 2000, S. 921–923, ISSN 0197-3851. PMID 11113897.
A. G. Tsiotou, A. Malisiova, E. Kalliardou: Anaesthesia and orphan disease: the child with 3M syndrome. In: European journal of anaesthesiology. Band 29, Nummer 12, Dezember 2012, S. 598–600, ISSN 1365-2346. doi:10.1097/EJA.0b013e32835a9a6c. PMID 23080434.

Eintrag zu 3M-Syndrom. In: Orphanet (Datenbank für seltene Krankheiten), abgerufen am 28. Juli 2024.

J. D. Miller, V. A. McKusick, P. Malvaux, S. Temtamy, C. Salinas: The 3-M syndrome: a heritable low birthweight dwarfism. In: Birth defects original article series. Band 11, Nummer 5, 1975, S. 39–47, ISSN 0547-6844. PMID 1218233.
F. Meo, V. Pinto, V. D’Addario: 3-M syndrome: a prenatal ultrasonographic diagnosis. In: Prenatal diagnosis. Band 20, Nummer 11, November 2000, S. 921–923, ISSN 0197-3851. PMID 11113897.
A. G. Tsiotou, A. Malisiova, E. Kalliardou: Anaesthesia and orphan disease: the child with 3M syndrome. In: European journal of anaesthesiology. Band 29, Nummer 12, Dezember 2012, S. 598–600, ISSN 1365-2346. doi:10.1097/EJA.0b013e32835a9a6c. PMID 23080434.