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4.0 étoiles sur 5 de 475 notations client
2001-12-01
Hope and Destiny: A Patient's and Parent's Guide to Sickle Cell Disease and Sickle Cell Trait - de Alan Sacerdote, Allen Platt (Author)
Caractéristiques Hope and Destiny: A Patient's and Parent's Guide to Sickle Cell Disease and Sickle Cell Trait
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Le Titre Du Fichier | Hope and Destiny: A Patient's and Parent's Guide to Sickle Cell Disease and Sickle Cell Trait |
Date de publication | 2001-12-01 |
Traducteur | Kaisie Elio |
Numéro de Pages | 401 Pages |
La taille du fichier | 30.16 MB |
Langage | Anglais & Français |
Éditeur | Shambhala |
ISBN-10 | 0556035657-TPK |
Type de E-Book | ePub AMZ PDF CWK Mobi |
de (Auteur) | Alan Sacerdote, Allen Platt |
Digital ISBN | 182-0839543594-IVO |
Nom de Fichier | Hope-and-Destiny-A-Patient's-and-Parent's-Guide-to-Sickle-Cell-Disease-and-Sickle-Cell-Trait.pdf |
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Hope and Destiny The Patient and Parent s Guide to Sickle Cell Disease and Sickle Cell Trait book
Noté 005 Retrouvez Hope and Destiny The Patient and Parents Guide to Sickle Cell Disease and Sickle Cell Trait by Platt Jr C Allan F Eckman Dr James 2011 Paperback et des millions de livres en stock sur Achetez neuf ou doccasion
Noté 005 Retrouvez Hope and Destiny The Patient and Parents Guide to Sickle Cell Disease and Sickle Cell Trait et des millions de livres en stock sur Achetez neuf ou doccasion
Noté 005 Retrouvez Hope and Destiny A Patients and Parents Guide to Sickle Cell Disease and Sickle Cell Trait et des millions de livres en stock sur Achetez neuf ou doccasion
PDF Hope and Destiny The Patient and Parent s Guide to Sickle Cell Disease and Sickle Cell
Hi I have a 4 month old baby girl and I found out she has SC when she was born I read alot and I just want to know what to expect from someone living with the disease Im concerned about daycare infections colds sports how to know if she is in pain I appreciate any advice
Neonatal screening for sickle cell disease SCD the most common of recessive autosomic hemoglobin disorders allows detection of affected babies homozygous sickle cell disease compound heterozygote SC and S bthalassemia in a target population