متلازمة موات ويلسون (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "متلازمة موات ويلسون" in Arabic language version.

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Mowat، DR؛ Croaker، GD؛ Cass، DT؛ Kerr، BA؛ Chaitow، J؛ Adès، LC؛ Chia، NL؛ Wilson، MJ (1998). "Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: Delineation of a new syndrome and identification of a locus at chromosome 2q22-q23". Journal of Medical Genetics. ج. 35 ع. 8: 617–23. DOI:10.1136/jmg.35.8.617. PMC:1051383. PMID:9719364.
Cordelli، DM؛ Garavelli، L؛ Savasta، S؛ Guerra، A؛ Pellicciari، A؛ Giordano، L؛ Bonetti، S؛ Cecconi، I؛ وآخرون (2013). "Epilepsy in Mowat-Wilson syndrome: Delineation of the electroclinical phenotype". American Journal of Medical Genetics Part A. ج. 161A ع. 2: 273–84. DOI:10.1002/ajmg.a.35717. PMID:23322667.

Mowat، DR؛ Croaker، GD؛ Cass، DT؛ Kerr، BA؛ Chaitow، J؛ Adès، LC؛ Chia، NL؛ Wilson، MJ (1998). "Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: Delineation of a new syndrome and identification of a locus at chromosome 2q22-q23". Journal of Medical Genetics. ج. 35 ع. 8: 617–23. DOI:10.1136/jmg.35.8.617. PMC:1051383. PMID:9719364.
Cordelli، DM؛ Garavelli، L؛ Savasta، S؛ Guerra، A؛ Pellicciari، A؛ Giordano، L؛ Bonetti، S؛ Cecconi، I؛ وآخرون (2013). "Epilepsy in Mowat-Wilson syndrome: Delineation of the electroclinical phenotype". American Journal of Medical Genetics Part A. ج. 161A ع. 2: 273–84. DOI:10.1002/ajmg.a.35717. PMID:23322667.