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Familial Hypoplastic Anaemia with Congenital Abnormalities (Fanconi's Syndrome): Report of a Case

Detalles Bibliográficos
Autor principal: McAlpine, Stuart G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Medico-Chirurgical Society of Glasgow 1954
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5973674/
https://www.ncbi.nlm.nih.gov/pubmed/13151451
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author McAlpine, Stuart G.
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spelling pubmed-59736742018-11-15 Familial Hypoplastic Anaemia with Congenital Abnormalities (Fanconi's Syndrome): Report of a Case McAlpine, Stuart G. Glasgow Med J Clinical Memoranda Royal Medico-Chirurgical Society of Glasgow 1954-02 /pmc/articles/PMC5973674/ /pubmed/13151451 Text en http://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) , which permits non-commercial use and redistribution provided that the original author and source are credited.
spellingShingle Clinical Memoranda
McAlpine, Stuart G.
Familial Hypoplastic Anaemia with Congenital Abnormalities (Fanconi's Syndrome): Report of a Case
title Familial Hypoplastic Anaemia with Congenital Abnormalities (Fanconi's Syndrome): Report of a Case
title_full Familial Hypoplastic Anaemia with Congenital Abnormalities (Fanconi's Syndrome): Report of a Case
title_fullStr Familial Hypoplastic Anaemia with Congenital Abnormalities (Fanconi's Syndrome): Report of a Case
title_full_unstemmed Familial Hypoplastic Anaemia with Congenital Abnormalities (Fanconi's Syndrome): Report of a Case
title_short Familial Hypoplastic Anaemia with Congenital Abnormalities (Fanconi's Syndrome): Report of a Case
title_sort familial hypoplastic anaemia with congenital abnormalities (fanconi's syndrome): report of a case
topic Clinical Memoranda
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5973674/
https://www.ncbi.nlm.nih.gov/pubmed/13151451
work_keys_str_mv AT mcalpinestuartg familialhypoplasticanaemiawithcongenitalabnormalitiesfanconissyndromereportofacase