Börjeson–Forssman–Lehmann syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Börjeson–Forssman–Lehmann syndrome" in English language version.

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1rarediseases.org

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1socialstyrelsen.se

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bmj.com

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Zweier, Christiane; Kraus, Cornelia; Brueton, Louise; Cole, Trevor; Degenhardt, Franziska; Engels, Hartmut; Gillessen-Kaesbach, Gabriele; Graul-Neumann, Luitgard; Horn, Denise; Hoyer, Juliane; Just, Walter; Rauch, Anita; Reis, André; Wollnik, Bernd; Zeschnigk, Michael (2013-12-01). "A new face of Borjeson–Forssman–Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype". Journal of Medical Genetics. 50 (12): 838–847. doi:10.1136/jmedgenet-2013-101918. ISSN 0022-2593. PMID 24092917. S2CID 44490262.

doi.org

Zweier, Christiane; Kraus, Cornelia; Brueton, Louise; Cole, Trevor; Degenhardt, Franziska; Engels, Hartmut; Gillessen-Kaesbach, Gabriele; Graul-Neumann, Luitgard; Horn, Denise; Hoyer, Juliane; Just, Walter; Rauch, Anita; Reis, André; Wollnik, Bernd; Zeschnigk, Michael (2013-12-01). "A new face of Borjeson–Forssman–Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype". Journal of Medical Genetics. 50 (12): 838–847. doi:10.1136/jmedgenet-2013-101918. ISSN 0022-2593. PMID 24092917. S2CID 44490262.

nih.gov

pubmed.ncbi.nlm.nih.gov

Zweier, Christiane; Kraus, Cornelia; Brueton, Louise; Cole, Trevor; Degenhardt, Franziska; Engels, Hartmut; Gillessen-Kaesbach, Gabriele; Graul-Neumann, Luitgard; Horn, Denise; Hoyer, Juliane; Just, Walter; Rauch, Anita; Reis, André; Wollnik, Bernd; Zeschnigk, Michael (2013-12-01). "A new face of Borjeson–Forssman–Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype". Journal of Medical Genetics. 50 (12): 838–847. doi:10.1136/jmedgenet-2013-101918. ISSN 0022-2593. PMID 24092917. S2CID 44490262.

orpha.net

"Orphanet: Borjeson Forssman Lehmann syndrome". Orphanet. Retrieved 2015-07-24.

rarediseases.org

"Börjeson-Forssman-Lehman Syndrome - NORD (National Organization for Rare Disorders)". Retrieved 2015-07-25.

semanticscholar.org

api.semanticscholar.org

Zweier, Christiane; Kraus, Cornelia; Brueton, Louise; Cole, Trevor; Degenhardt, Franziska; Engels, Hartmut; Gillessen-Kaesbach, Gabriele; Graul-Neumann, Luitgard; Horn, Denise; Hoyer, Juliane; Just, Walter; Rauch, Anita; Reis, André; Wollnik, Bernd; Zeschnigk, Michael (2013-12-01). "A new face of Borjeson–Forssman–Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype". Journal of Medical Genetics. 50 (12): 838–847. doi:10.1136/jmedgenet-2013-101918. ISSN 0022-2593. PMID 24092917. S2CID 44490262.

socialstyrelsen.se

"Börjeson-Forssman-Lehmann syndrome". www.socialstyrelsen.se. Archived from the original on 2019-04-08. Retrieved 2015-07-24.

web.archive.org

"Börjeson-Forssman-Lehmann syndrome". www.socialstyrelsen.se. Archived from the original on 2019-04-08. Retrieved 2015-07-24.

worldcat.org

search.worldcat.org

Zweier, Christiane; Kraus, Cornelia; Brueton, Louise; Cole, Trevor; Degenhardt, Franziska; Engels, Hartmut; Gillessen-Kaesbach, Gabriele; Graul-Neumann, Luitgard; Horn, Denise; Hoyer, Juliane; Just, Walter; Rauch, Anita; Reis, André; Wollnik, Bernd; Zeschnigk, Michael (2013-12-01). "A new face of Borjeson–Forssman–Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype". Journal of Medical Genetics. 50 (12): 838–847. doi:10.1136/jmedgenet-2013-101918. ISSN 0022-2593. PMID 24092917. S2CID 44490262.