متلازمة انعدام الأصابع وخلل التنسج الأديمي (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "متلازمة انعدام الأصابع وخلل التنسج الأديمي" in Arabic language version.

refsWebsite

Global rank Arabic rank

10nih.gov

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7doi.org

2^nd place

5^th place

1web.archive.org

1^st place

1semanticscholar.org

11^th place

86^th place

1qut.edu.au

8,570^th place

7,432^nd place

1archive.org

6^th place

3^rd place

archive.org (Global: 6^th place; Arabic: 3^rd place)

Shprintzen، Robert J. (1997). Genetics, Syndromes, and Communication Disorders. Singular Pub. Group. ISBN:978-1-56593-620-1.

doi.org (Global: 2^nd place; Arabic: 5^th place)

Buss PW، Hughes HE، Clarke A (سبتمبر 1995). "Twenty-four cases of the EEC syndrome: clinical presentation and management". Journal of Medical Genetics. ج. 32 ع. 9: 716–723. DOI:10.1136/jmg.32.9.716. PMC:1051673. PMID:8544192.
Celli J، Duijf P، Hamel BC، وآخرون (1999). "Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome" (PDF). Cell. ج. 99 ع. 2: 143–153. DOI:10.1016/S0092-8674(00)81646-3. PMID:10535733. S2CID:18193864. مؤرشف من الأصل (PDF) في 2020-12-24.
Brunner HG، Hamel BC، Van Bokhoven H (2002). "The p63 gene in EEC and other syndromes". Journal of Medical Genetics. ج. 39 ع. 6: 377–381. DOI:10.1136/jmg.39.6.377. PMC:1735150. PMID:12070241.
Moerman P، Fryns JP (1996). "Ectodermal dysplasia, Rapp–Hodgkin type in a mother and severe ectrodactyly–ectodermal dysplasia–clefting syndrome (EEC) in her child". American Journal of Medical Genetics. ج. 63 ع. 3: 479–481. DOI:10.1002/(SICI)1096-8628(19960614)63:3<479::AID-AJMG12>3.0.CO;2-J. PMID:8737656.
Ruhin B، Martinot V، Lafforgue P، Catteau B، Manouvrier-Hanu S، Ferri J (2001). "Pure ectodermal dysplasia: retrospective study of 16 cases and literature review". Cleft Palate-Craniofacial Journal. ج. 38 ع. 5: 504–518. DOI:10.1597/1545-1569(2001)038<0504:PEDRSO>2.0.CO;2. PMID:11522173.
Peterson-Falzone SJ، Caldarelli DD، Landahl KL (1981). "Abnormal laryngeal vocal quality in ectodermal dysplasia". Archives of Otolaryngology. ج. 107 ع. 5: 300–304. DOI:10.1001/archotol.1981.00790410038010. PMID:7224950.
O'Quinn JR، Hennekam RC، Jorde LB، Bamshad M (1998). "Syndromic ectrodactyly with severe limb, ectodermal, urogenital, and palatal defects maps to chromosome 19". American Journal of Human Genetics. ج. 62 ع. 1: 130–135. DOI:10.1086/301687. PMC:1376811. PMID:9443880.

nih.gov (Global: 4^th place; Arabic: 6^th place)

pubmed.ncbi.nlm.nih.gov

Buss PW، Hughes HE، Clarke A (سبتمبر 1995). "Twenty-four cases of the EEC syndrome: clinical presentation and management". Journal of Medical Genetics. ج. 32 ع. 9: 716–723. DOI:10.1136/jmg.32.9.716. PMC:1051673. PMID:8544192.
Celli J، Duijf P، Hamel BC، وآخرون (1999). "Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome" (PDF). Cell. ج. 99 ع. 2: 143–153. DOI:10.1016/S0092-8674(00)81646-3. PMID:10535733. S2CID:18193864. مؤرشف من الأصل (PDF) في 2020-12-24.
Brunner HG، Hamel BC، Van Bokhoven H (2002). "The p63 gene in EEC and other syndromes". Journal of Medical Genetics. ج. 39 ع. 6: 377–381. DOI:10.1136/jmg.39.6.377. PMC:1735150. PMID:12070241.
Moerman P، Fryns JP (1996). "Ectodermal dysplasia, Rapp–Hodgkin type in a mother and severe ectrodactyly–ectodermal dysplasia–clefting syndrome (EEC) in her child". American Journal of Medical Genetics. ج. 63 ع. 3: 479–481. DOI:10.1002/(SICI)1096-8628(19960614)63:3<479::AID-AJMG12>3.0.CO;2-J. PMID:8737656.
Ruhin B، Martinot V، Lafforgue P، Catteau B، Manouvrier-Hanu S، Ferri J (2001). "Pure ectodermal dysplasia: retrospective study of 16 cases and literature review". Cleft Palate-Craniofacial Journal. ج. 38 ع. 5: 504–518. DOI:10.1597/1545-1569(2001)038<0504:PEDRSO>2.0.CO;2. PMID:11522173.
Peterson-Falzone SJ، Caldarelli DD، Landahl KL (1981). "Abnormal laryngeal vocal quality in ectodermal dysplasia". Archives of Otolaryngology. ج. 107 ع. 5: 300–304. DOI:10.1001/archotol.1981.00790410038010. PMID:7224950.
O'Quinn JR، Hennekam RC، Jorde LB، Bamshad M (1998). "Syndromic ectrodactyly with severe limb, ectodermal, urogenital, and palatal defects maps to chromosome 19". American Journal of Human Genetics. ج. 62 ع. 1: 130–135. DOI:10.1086/301687. PMC:1376811. PMID:9443880.

ncbi.nlm.nih.gov

Buss PW، Hughes HE، Clarke A (سبتمبر 1995). "Twenty-four cases of the EEC syndrome: clinical presentation and management". Journal of Medical Genetics. ج. 32 ع. 9: 716–723. DOI:10.1136/jmg.32.9.716. PMC:1051673. PMID:8544192.
Brunner HG، Hamel BC، Van Bokhoven H (2002). "The p63 gene in EEC and other syndromes". Journal of Medical Genetics. ج. 39 ع. 6: 377–381. DOI:10.1136/jmg.39.6.377. PMC:1735150. PMID:12070241.
O'Quinn JR، Hennekam RC، Jorde LB، Bamshad M (1998). "Syndromic ectrodactyly with severe limb, ectodermal, urogenital, and palatal defects maps to chromosome 19". American Journal of Human Genetics. ج. 62 ع. 1: 130–135. DOI:10.1086/301687. PMC:1376811. PMID:9443880.

qut.edu.au (Global: 8,570^th place; Arabic: 7,432^nd place)

eprints.qut.edu.au

Celli J، Duijf P، Hamel BC، وآخرون (1999). "Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome" (PDF). Cell. ج. 99 ع. 2: 143–153. DOI:10.1016/S0092-8674(00)81646-3. PMID:10535733. S2CID:18193864. مؤرشف من الأصل (PDF) في 2020-12-24.

semanticscholar.org (Global: 11^th place; Arabic: 86^th place)

api.semanticscholar.org

Celli J، Duijf P، Hamel BC، وآخرون (1999). "Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome" (PDF). Cell. ج. 99 ع. 2: 143–153. DOI:10.1016/S0092-8674(00)81646-3. PMID:10535733. S2CID:18193864. مؤرشف من الأصل (PDF) في 2020-12-24.

web.archive.org (Global: 1^st place; Arabic: 1^st place)

Celli J، Duijf P، Hamel BC، وآخرون (1999). "Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome" (PDF). Cell. ج. 99 ع. 2: 143–153. DOI:10.1016/S0092-8674(00)81646-3. PMID:10535733. S2CID:18193864. مؤرشف من الأصل (PDF) في 2020-12-24.

متلازمة انعدام الأصابع وخلل التنسج الأديمي (Arabic Wikipedia)

archive.org (Global: 6th place; Arabic: 3rd place)

doi.org (Global: 2nd place; Arabic: 5th place)

nih.gov (Global: 4th place; Arabic: 6th place)