E-LIB Suche - Ergebnisse für: Cole, William G.

1

Primary osteoporosis without features of OI in children and..:

Laine, Christine M. ; Koltin, Dror ; Susic, Miki...
American Journal of Medical Genetics Part A. 158A (2012) 6 - p. 1252-1261 , 2012

Link: https://doi.org/10.1002/..

2

Bone Matrix and Mineralization:

, In: Pediatric Bone,

McKee, Marc D. ; Cole, William G. - p. 9-37 , 2012

Link: https://doi.org/10.1016/..

3

List of Contributors:

, In: Pediatric Bone,

Adams, Judith E. ; Bachrach, Laura K. ; Bastepe, Murat... - p. xi-xiii , 2012

Link: https://doi.org/10.1016/..

4

Mutations in LRP5 cause primary osteoporosis without featur..:

Korvala, Johanna ; Jüppner, Harald ; Mäkitie, Outi...
BMC Medical Genetics. 13 (2012) 1 - p. , 2012

Link: https://doi.org/10.1186/..

5

Rare variations in WNT3A and DKK1 may predispose carriers t..:

Korvala, Johanna ; Löija, Marika ; Mäkitie, Outi...
European Journal of Medical Genetics. 55 (2012) 10 - p. 515-519 , 2012

Link: https://doi.org/10.1016/..

6

How Stand Productivity Results from Size- and Competition-D..:

Caspersen, John P. ; Vanderwel, Mark C. ; Cole, William G...
PLoS ONE. 6 (2011) 12 - p. e28660 , 2011

Link: https://doi.org/10.1371/..

7

Mutations in TRPV4 cause an inherited arthropathy of hands ..:

Lamandé, Shireen R ; Yuan, Yuan ; Gresshoff, Irma L...
Nature Genetics. 43 (2011) 11 - p. 1142-1146 , 2011

Link: https://doi.org/10.1038/..

8

Early‐onset metaphyseal chondrodysplasia type Schmid associ..:

Mäkitie, Outi ; Susic, Miki ; Cole, William G.
Journal of Orthopaedic Research. 28 (2010) 11 - p. 1497-1501 , 2010

Link: https://doi.org/10.1002/..

9

Low density lipoprotein receptor‐related protein 5 (LRP5) m..:

Saarinen, Anne ; Saukkonen, Tero ; Kivelä, Tero...
Clinical Endocrinology. 72 (2010) 4 - p. 481-488 , 2010

Link: https://doi.org/10.1111/..

10

Long-term clinical outcome and carrier phenotype in autosom..:

Mäkitie, Outi ; Pereira, Renata C ; Kaitila, Ilkka...
Journal of Bone and Mineral Research. 25 (2010) 10 - p. 2165-2174 , 2010

Link: https://doi.org/10.1002/..

11

Characterization of the six zebrafish clade B fibrillar pro..:

Hoffman, Guy G. ; Branam, Amanda M. ; Huang, Guorui...
Matrix Biology. 29 (2010) 4 - p. 261-275 , 2010

Link: https://doi.org/10.1016/..

12

Absence of apparent disease causing mutations in COL5A3 in ..:

Hoffman, Guy G. ; Dodson, Gerald E. ; Cole, William G..
American Journal of Medical Genetics Part A. 146A (2008) 24 - p. 3240-3241 , 2008

Link: https://doi.org/10.1002/..

13

COL10A1 nonsense and frame-shift mutations have a gain-of-f..:

Ho, Matthew S.P. ; Tsang, Kwok Yeung ; Lo, Rebecca L.K....
Human Molecular Genetics. 16 (2007) 10 - p. 1201-1215 , 2007

Link: https://doi.org/10.1093/..

14

Shwachman–Diamond syndrome is associated with low-turnover ..:

Toiviainen-Salo, Sanna ; Mäyränpää, Mervi K. ; Durie, Peter R....
Bone. 41 (2007) 6 - p. 965-972 , 2007

Link: https://doi.org/10.1016/..

15

HOXD10 M319K mutation in a family with isolated congenital ..:

Dobbs, Matthew B. ; Gurnett, Christina A. ; Pierce, Brandon...
Journal of Orthopaedic Research. 24 (2006) 3 - p. 448-453 , 2006

Link: https://doi.org/10.1002/..