L1CAM-Syndrom (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "L1CAM-Syndrom" in German language version.

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F. J. Gareis, J. D. Mason: X-linked mental retardation associated with bilateral clasp thumb anomaly. In: American journal of medical genetics. Band 17, Nummer 1, Januar 1984, S. 333–338, ISSN 0148-7299. doi:10.1002/ajmg.1320170126. PMID 6538753.
P. J. Willems, O. F. Brouwer, I. Dijkstra, J. Wilmink: X-linked hydrocephalus. In: American journal of medical genetics. Band 27, Nummer 4, August 1987, S. 921–928, ISSN 0148-7299. doi:10.1002/ajmg.1320270419. PMID 3425602.

E. Fransen, V. Lemmon, G. Van Camp, L. Vits, P. Coucke, P. J. Willems: CRASH syndrome: clinical spectrum of corpus callosum hypoplasia, retardation, adducted thumbs, spastic paraparesis and hydrocephalus due to mutations in one single gene, L1. In: European journal of human genetics : EJHG. Band 3, Nummer 5, 1995, S. 273–284, ISSN 1018-4813. PMID 8556302. (Review).
F. J. Gareis, J. D. Mason: X-linked mental retardation associated with bilateral clasp thumb anomaly. In: American journal of medical genetics. Band 17, Nummer 1, Januar 1984, S. 333–338, ISSN 0148-7299. doi:10.1002/ajmg.1320170126. PMID 6538753.
GeneReviews
C. Schrander-Stumpel, J. P. Fryns: Congenital hydrocephalus: nosology and guidelines for clinical approach and genetic counselling. In: European Journal of Pediatrics. Band 157, Nummer 5, Mai 1998, S. 355–362, ISSN 0340-6199. PMID 9625330. (Review).
J. W. Bianchine, R. C. Lewis: The MASA syndrome: a new heritable mental retardation syndrome. In: Clinical genetics. Band 5, Nummer 4, 1974, S. 298–306, ISSN 0009-9163. PMID 4855169.
P. J. Willems, O. F. Brouwer, I. Dijkstra, J. Wilmink: X-linked hydrocephalus. In: American journal of medical genetics. Band 27, Nummer 4, August 1987, S. 921–928, ISSN 0148-7299. doi:10.1002/ajmg.1320270419. PMID 3425602.

E. Fransen, V. Lemmon, G. Van Camp, L. Vits, P. Coucke, P. J. Willems: CRASH syndrome: clinical spectrum of corpus callosum hypoplasia, retardation, adducted thumbs, spastic paraparesis and hydrocephalus due to mutations in one single gene, L1. In: European journal of human genetics : EJHG. Band 3, Nummer 5, 1995, S. 273–284, ISSN 1018-4813. PMID 8556302. (Review).
F. J. Gareis, J. D. Mason: X-linked mental retardation associated with bilateral clasp thumb anomaly. In: American journal of medical genetics. Band 17, Nummer 1, Januar 1984, S. 333–338, ISSN 0148-7299. doi:10.1002/ajmg.1320170126. PMID 6538753.
C. Schrander-Stumpel, J. P. Fryns: Congenital hydrocephalus: nosology and guidelines for clinical approach and genetic counselling. In: European Journal of Pediatrics. Band 157, Nummer 5, Mai 1998, S. 355–362, ISSN 0340-6199. PMID 9625330. (Review).
J. W. Bianchine, R. C. Lewis: The MASA syndrome: a new heritable mental retardation syndrome. In: Clinical genetics. Band 5, Nummer 4, 1974, S. 298–306, ISSN 0009-9163. PMID 4855169.
P. J. Willems, O. F. Brouwer, I. Dijkstra, J. Wilmink: X-linked hydrocephalus. In: American journal of medical genetics. Band 27, Nummer 4, August 1987, S. 921–928, ISSN 0148-7299. doi:10.1002/ajmg.1320270419. PMID 3425602.