Donnai–Barrow syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Donnai–Barrow syndrome" in English language version.

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Donnai, D; Barrow, M (1993). "Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness: a newly recognized autosomal recessive disorder?". American Journal of Medical Genetics. 47 (5): 679–682. doi:10.1002/ajmg.1320470518. PMID 8266995.
Kantarci S; Al-Gazali L; Hill RS; et al. (August 2007). "Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes". Nat. Genet. 39 (8): 957–9. doi:10.1038/ng2063. PMC 2891728. PMID 17632512.
The sources below were used to develop this article's condition summary on Donnai-Barrow syndrome.
- Chassaing, N; Lacombe, D; Carles, D; Calvas, P; Saura, R; Bieth, E (2003). "Donnai-Barrow syndrome: four additional patients". American Journal of Medical Genetics Part A. 121A (3): 258–62. doi:10.1002/ajmg.a.20266. PMID 12923867. S2CID 38409652.

"Donnai-Barrow syndrome" (online). MedlinePlus. U.S. National Library of Medicine of the National Institutes of Health. 1 April 2013. Archived from the original on 2020-10-21. Retrieved 8 May 2021. This article incorporates text from the United States National Library of Medicine, which is in the public domain.

Donnai, D; Barrow, M (1993). "Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness: a newly recognized autosomal recessive disorder?". American Journal of Medical Genetics. 47 (5): 679–682. doi:10.1002/ajmg.1320470518. PMID 8266995.
Kantarci S; Al-Gazali L; Hill RS; et al. (August 2007). "Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes". Nat. Genet. 39 (8): 957–9. doi:10.1038/ng2063. PMC 2891728. PMID 17632512.
The sources below were used to develop this article's condition summary on Donnai-Barrow syndrome.
- Chassaing, N; Lacombe, D; Carles, D; Calvas, P; Saura, R; Bieth, E (2003). "Donnai-Barrow syndrome: four additional patients". American Journal of Medical Genetics Part A. 121A (3): 258–62. doi:10.1002/ajmg.a.20266. PMID 12923867. S2CID 38409652.
ncbi.nlm.nih.gov
- Kantarci S; Al-Gazali L; Hill RS; et al. (August 2007). "Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes". Nat. Genet. 39 (8): 957–9. doi:10.1038/ng2063. PMC 2891728. PMID 17632512.

The sources below were used to develop this article's condition summary on Donnai-Barrow syndrome.
- Chassaing, N; Lacombe, D; Carles, D; Calvas, P; Saura, R; Bieth, E (2003). "Donnai-Barrow syndrome: four additional patients". American Journal of Medical Genetics Part A. 121A (3): 258–62. doi:10.1002/ajmg.a.20266. PMID 12923867. S2CID 38409652.

"Donnai-Barrow syndrome" (online). MedlinePlus. U.S. National Library of Medicine of the National Institutes of Health. 1 April 2013. Archived from the original on 2020-10-21. Retrieved 8 May 2021. This article incorporates text from the United States National Library of Medicine, which is in the public domain.