متلازمة سنيدرز بلوك كامبو (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "متلازمة سنيدرز بلوك كامبو" in Arabic language version.

refsWebsite

Global rank Arabic rank

12nih.gov

4^th place

6^th place

6doi.org

2^nd place

5^th place

5worldcat.org

5^th place

4^th place

3web.archive.org

1^st place

1harvard.edu

18^th place

33^rd place

1semanticscholar.org

11^th place

86^th place

1medlineplus.gov

1,581^st place

332^nd place

doi.org

Fan، Xi-Yong (15 سبتمبر 2021). "Snijders Blok-Campeau syndrome caused by CHD3 gene mutation: a case report". Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics. ج. 23 ع. 9: 965–968. DOI:10.7499/j.issn.1008-8830.2106091. ISSN:1008-8830. PMC:8480161. PMID:34535214.
Snijders Blok، Lot؛ Rousseau، Justine؛ Twist، Joanna؛ Ehresmann، Sophie؛ Takaku، Motoki؛ Venselaar، Hanka؛ Rodan، Lance H.؛ Nowak، Catherine B.؛ Douglas، Jessica؛ Swoboda، Kathryn J.؛ Steeves، Marcie A. (5 نوفمبر 2018). "CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language". Nature Communications. ج. 9 ع. 1: 4619. Bibcode:2018NatCo...9.4619S. DOI:10.1038/s41467-018-06014-6. ISSN:2041-1723. PMC:6218476. PMID:30397230.
Hoffmann، Anke؛ Spengler، Dietmar (24 يوليو 2019). "Chromatin Remodeling Complex NuRD in Neurodevelopment and Neurodevelopmental Disorders". Front Genet. ج. 10: 682. DOI:10.3389/fgene.2019.00682. PMC:6667665. PMID:31396263.
Malinger، Gustavo؛ Hoffmann، Chen؛ Achiron، Reuven؛ Berkenstadt، Michal (2021). "Prenatal Diagnosis of Snijders Blok-Campeau Syndrome in a Fetus with Macrocephaly". Fetal Diagnosis and Therapy. ج. 48 ع. 5: 407–410. DOI:10.1159/000514326. ISSN:1421-9964. PMID:34000720. S2CID:234768265. مؤرشف من الأصل في 2022-07-20.
Drivas، Theodore G.؛ Li، Dong؛ Nair، Divya؛ Alaimo، Joseph T.؛ Alders، Mariëlle؛ Altmüller، Janine؛ Barakat، Tahsin Stefan؛ Bebin، E. Martina؛ Bertsch، Nicole L.؛ Blackburn، Patrick R.؛ Blesson، Alyssa (أكتوبر 2020). "A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome". European Journal of Human Genetics. ج. 28 ع. 10: 1422–1431. DOI:10.1038/s41431-020-0654-4. ISSN:1476-5438. PMC:7608102. PMID:32483341.
Hoffmann، Anke؛ Spengler، Dietmar (2019). "Chromatin Remodeling Complex NuRD in Neurodevelopment and Neurodevelopmental Disorders". Frontiers in Genetics. ج. 10: 682. DOI:10.3389/fgene.2019.00682. ISSN:1664-8021. PMC:6667665. PMID:31396263.

harvard.edu

ui.adsabs.harvard.edu

Snijders Blok، Lot؛ Rousseau، Justine؛ Twist، Joanna؛ Ehresmann، Sophie؛ Takaku، Motoki؛ Venselaar، Hanka؛ Rodan، Lance H.؛ Nowak، Catherine B.؛ Douglas، Jessica؛ Swoboda، Kathryn J.؛ Steeves، Marcie A. (5 نوفمبر 2018). "CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language". Nature Communications. ج. 9 ع. 1: 4619. Bibcode:2018NatCo...9.4619S. DOI:10.1038/s41467-018-06014-6. ISSN:2041-1723. PMC:6218476. PMID:30397230.

medlineplus.gov

"Snijders Blok-Campeau syndrome: MedlinePlus Genetics". medlineplus.gov (بالإنجليزية). Archived from the original on 2023-04-20. Retrieved 2022-07-20.

nih.gov

ncbi.nlm.nih.gov

Fan، Xi-Yong (15 سبتمبر 2021). "Snijders Blok-Campeau syndrome caused by CHD3 gene mutation: a case report". Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics. ج. 23 ع. 9: 965–968. DOI:10.7499/j.issn.1008-8830.2106091. ISSN:1008-8830. PMC:8480161. PMID:34535214.
"Snijders Blok-Campeau syndrome (Concept Id: C4748701) - MedGen - NCBI". www.ncbi.nlm.nih.gov (بالإنجليزية). Archived from the original on 2023-04-20. Retrieved 2022-07-20.
Snijders Blok، Lot؛ Rousseau، Justine؛ Twist، Joanna؛ Ehresmann، Sophie؛ Takaku، Motoki؛ Venselaar، Hanka؛ Rodan، Lance H.؛ Nowak، Catherine B.؛ Douglas، Jessica؛ Swoboda، Kathryn J.؛ Steeves، Marcie A. (5 نوفمبر 2018). "CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language". Nature Communications. ج. 9 ع. 1: 4619. Bibcode:2018NatCo...9.4619S. DOI:10.1038/s41467-018-06014-6. ISSN:2041-1723. PMC:6218476. PMID:30397230.
Hoffmann، Anke؛ Spengler، Dietmar (24 يوليو 2019). "Chromatin Remodeling Complex NuRD in Neurodevelopment and Neurodevelopmental Disorders". Front Genet. ج. 10: 682. DOI:10.3389/fgene.2019.00682. PMC:6667665. PMID:31396263.
Drivas، Theodore G.؛ Li، Dong؛ Nair، Divya؛ Alaimo، Joseph T.؛ Alders، Mariëlle؛ Altmüller، Janine؛ Barakat، Tahsin Stefan؛ Bebin، E. Martina؛ Bertsch، Nicole L.؛ Blackburn، Patrick R.؛ Blesson، Alyssa (أكتوبر 2020). "A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome". European Journal of Human Genetics. ج. 28 ع. 10: 1422–1431. DOI:10.1038/s41431-020-0654-4. ISSN:1476-5438. PMC:7608102. PMID:32483341.
Hoffmann، Anke؛ Spengler، Dietmar (2019). "Chromatin Remodeling Complex NuRD in Neurodevelopment and Neurodevelopmental Disorders". Frontiers in Genetics. ج. 10: 682. DOI:10.3389/fgene.2019.00682. ISSN:1664-8021. PMC:6667665. PMID:31396263.

pubmed.ncbi.nlm.nih.gov

Fan، Xi-Yong (15 سبتمبر 2021). "Snijders Blok-Campeau syndrome caused by CHD3 gene mutation: a case report". Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics. ج. 23 ع. 9: 965–968. DOI:10.7499/j.issn.1008-8830.2106091. ISSN:1008-8830. PMC:8480161. PMID:34535214.
Snijders Blok، Lot؛ Rousseau، Justine؛ Twist، Joanna؛ Ehresmann، Sophie؛ Takaku، Motoki؛ Venselaar، Hanka؛ Rodan، Lance H.؛ Nowak، Catherine B.؛ Douglas، Jessica؛ Swoboda، Kathryn J.؛ Steeves، Marcie A. (5 نوفمبر 2018). "CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language". Nature Communications. ج. 9 ع. 1: 4619. Bibcode:2018NatCo...9.4619S. DOI:10.1038/s41467-018-06014-6. ISSN:2041-1723. PMC:6218476. PMID:30397230.
Hoffmann، Anke؛ Spengler، Dietmar (24 يوليو 2019). "Chromatin Remodeling Complex NuRD in Neurodevelopment and Neurodevelopmental Disorders". Front Genet. ج. 10: 682. DOI:10.3389/fgene.2019.00682. PMC:6667665. PMID:31396263.
Malinger، Gustavo؛ Hoffmann، Chen؛ Achiron، Reuven؛ Berkenstadt، Michal (2021). "Prenatal Diagnosis of Snijders Blok-Campeau Syndrome in a Fetus with Macrocephaly". Fetal Diagnosis and Therapy. ج. 48 ع. 5: 407–410. DOI:10.1159/000514326. ISSN:1421-9964. PMID:34000720. S2CID:234768265. مؤرشف من الأصل في 2022-07-20.
Drivas، Theodore G.؛ Li، Dong؛ Nair، Divya؛ Alaimo، Joseph T.؛ Alders، Mariëlle؛ Altmüller، Janine؛ Barakat، Tahsin Stefan؛ Bebin، E. Martina؛ Bertsch، Nicole L.؛ Blackburn، Patrick R.؛ Blesson، Alyssa (أكتوبر 2020). "A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome". European Journal of Human Genetics. ج. 28 ع. 10: 1422–1431. DOI:10.1038/s41431-020-0654-4. ISSN:1476-5438. PMC:7608102. PMID:32483341.
Hoffmann، Anke؛ Spengler، Dietmar (2019). "Chromatin Remodeling Complex NuRD in Neurodevelopment and Neurodevelopmental Disorders". Frontiers in Genetics. ج. 10: 682. DOI:10.3389/fgene.2019.00682. ISSN:1664-8021. PMC:6667665. PMID:31396263.

semanticscholar.org

api.semanticscholar.org

Malinger، Gustavo؛ Hoffmann، Chen؛ Achiron، Reuven؛ Berkenstadt، Michal (2021). "Prenatal Diagnosis of Snijders Blok-Campeau Syndrome in a Fetus with Macrocephaly". Fetal Diagnosis and Therapy. ج. 48 ع. 5: 407–410. DOI:10.1159/000514326. ISSN:1421-9964. PMID:34000720. S2CID:234768265. مؤرشف من الأصل في 2022-07-20.

web.archive.org

"Snijders Blok-Campeau syndrome (Concept Id: C4748701) - MedGen - NCBI". www.ncbi.nlm.nih.gov (بالإنجليزية). Archived from the original on 2023-04-20. Retrieved 2022-07-20.
Malinger، Gustavo؛ Hoffmann، Chen؛ Achiron، Reuven؛ Berkenstadt، Michal (2021). "Prenatal Diagnosis of Snijders Blok-Campeau Syndrome in a Fetus with Macrocephaly". Fetal Diagnosis and Therapy. ج. 48 ع. 5: 407–410. DOI:10.1159/000514326. ISSN:1421-9964. PMID:34000720. S2CID:234768265. مؤرشف من الأصل في 2022-07-20.
"Snijders Blok-Campeau syndrome: MedlinePlus Genetics". medlineplus.gov (بالإنجليزية). Archived from the original on 2023-04-20. Retrieved 2022-07-20.

worldcat.org

Fan، Xi-Yong (15 سبتمبر 2021). "Snijders Blok-Campeau syndrome caused by CHD3 gene mutation: a case report". Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics. ج. 23 ع. 9: 965–968. DOI:10.7499/j.issn.1008-8830.2106091. ISSN:1008-8830. PMC:8480161. PMID:34535214.
Snijders Blok، Lot؛ Rousseau، Justine؛ Twist، Joanna؛ Ehresmann، Sophie؛ Takaku، Motoki؛ Venselaar، Hanka؛ Rodan، Lance H.؛ Nowak، Catherine B.؛ Douglas، Jessica؛ Swoboda، Kathryn J.؛ Steeves، Marcie A. (5 نوفمبر 2018). "CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language". Nature Communications. ج. 9 ع. 1: 4619. Bibcode:2018NatCo...9.4619S. DOI:10.1038/s41467-018-06014-6. ISSN:2041-1723. PMC:6218476. PMID:30397230.
Malinger، Gustavo؛ Hoffmann، Chen؛ Achiron، Reuven؛ Berkenstadt، Michal (2021). "Prenatal Diagnosis of Snijders Blok-Campeau Syndrome in a Fetus with Macrocephaly". Fetal Diagnosis and Therapy. ج. 48 ع. 5: 407–410. DOI:10.1159/000514326. ISSN:1421-9964. PMID:34000720. S2CID:234768265. مؤرشف من الأصل في 2022-07-20.
Drivas، Theodore G.؛ Li، Dong؛ Nair، Divya؛ Alaimo، Joseph T.؛ Alders، Mariëlle؛ Altmüller، Janine؛ Barakat، Tahsin Stefan؛ Bebin، E. Martina؛ Bertsch، Nicole L.؛ Blackburn، Patrick R.؛ Blesson، Alyssa (أكتوبر 2020). "A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome". European Journal of Human Genetics. ج. 28 ع. 10: 1422–1431. DOI:10.1038/s41431-020-0654-4. ISSN:1476-5438. PMC:7608102. PMID:32483341.
Hoffmann، Anke؛ Spengler، Dietmar (2019). "Chromatin Remodeling Complex NuRD in Neurodevelopment and Neurodevelopmental Disorders". Frontiers in Genetics. ج. 10: 682. DOI:10.3389/fgene.2019.00682. ISSN:1664-8021. PMC:6667665. PMID:31396263.