Language
English
German
^M
Dutch
Spanish
Title:
Thalassemias: models of genetic diseases
Source:
Science [0036-8075] Kolata, G B yr:1980
Basic
Sorry, no full text available...
Please use the document delivery service (see below)
Holding information
Holdings in library search engine
ALBERT
Document delivery
Request document via
Library/Bibliothek
Users interested in this article also expressed an interest in the following:
description
1.
Carella, M.
"Genetic diseases."
Minerva biotecnologica
14.3/4 (2002): 237-240.
description
2.
Naevdal, E.
"Optimal Screening for Genetic Diseases."
Economics and human biology
15 (2014): 129-139.
description
3.
Anonymous, Y.
"Genetic Diseases/Gene Regulation/Gene Therapy."
Journal of investigative dermatology
132.S1 (2012).
description
4.
Wilkie, Andrew O M M.
"Prevalence and complications of single-gene and chromosomal disorders in craniosynostosis."
Pediatrics
126.2 (2010): 391-400.
description
5.
Jeschke, Marc G.
"Pathophysiologic Response to Burns in the Elderly."
EBioMedicine
2.10 (2015): 1536-1548.
description
6.
Pang, Ronald T.K..
"Ethics/education: Designer babies."
Obstetrics, gynaecology & reproductive medicine
26.2 (2016): 59-60.
description
7.
Shaviro, S.
"GENETIC DISORDER."
Artforum international
42.5 (2004): 42-.
description
8.
Dondorp, W.
"Dynamics of prenatal screening: new developments challenging the ethical framework."
Bioethics
29.1.
description
9.
"Tracking the origins of "sporadic" genetic diseases."
Science
270.5239 (1995): 1120-.
description
10.
Dorland, William Alexander Newman.
"genetic disease."
Dorland's illustrated medical dictionary
(2011).
description
11.
Oliver, A.
"From Nudging to Budging: Using Behavioural Economics to Inform Public Sector Policy."
Journal of Social Policy
42.4 (2013): 685-700.
description
12.
Holmes, G.
"Early onset of craniosynostosis in an Apert mouse model reveals critical features of this pathology."
Developmental biology
328.2 (2009): 273-284.
description
13.
Reardon, W.
"Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome."
Nature genetics
8.1 (1994): 98-103.
description
14.
Ornitz, D.
"FGF signaling pathways in endochondral and intramembranous bone development and human genetic disease."
Genes & development
16.12: 1446-1465.
description
15.
van-Bokhoven, B.
"Erratum: Mutations in different components of FGF signaling in LADD syndrome."
Nature genetics
38.4: 495-495.
description
16.
Gillberg, C.
"Chromosomal Disorders and Autism."
Journal of autism and developmental disorders
28.5 (1998): 415-25.
View More...
View Less...
Select All
Clear All
Save Citations
Select Format
EndNote
RefWorks
Reference Manager
ProCite
Submit citation export
Advanced
Author
Other articles by this author? -- in
GeoRef
author:
Kolata, G B
last name
initials
Other articles by this author? -- in
Online Contents Geosciences
author:
Kolata, G B
last name
initials
Web Search
Find related information in
a Web Search Engine
Excite
Google
HotBot
Ixquick
ZOO
Ask
Yahoo!
Bing
Naver
Search Terms:
Search for related information in
Google Scholar
Article Title
Author Name
Journal Title
Other Search
Search Terms:
A service provided by the
Library of the Wissenschaftspark Albert Einstein
, Potsdam, Germany.
© 2005 SFX by Ex Libris Inc.