E-LIB Suche - Ergebnisse für: Campos-Xavier, B

1

Corrigendum to "Post-axial polydactyly type A2, overgrowth ..:

Kannu, P. ; Campos-Xavier, A.B. ; Hull, D....
European Journal of Medical Genetics. 57 (2014) 2-3 - p. 123-124 , 2014

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

2

Post-axial polydactyly type A2, overgrowth and autistic tra..:

Kannu, P. ; Campos-Xavier, A.B. ; Hull, D....
European Journal of Medical Genetics. 56 (2013) 8 - p. 452-457 , 2013

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

3

Identification of potential non-invasive biomarkers in dias..:

Paganini, C ; Carroll, R.S ; Gramegna Tota, C...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.bone.2023.116838. , 2023

Link: https://serval.unil.ch/n..

4

Correction to: New Dominant‑Negative IL6ST Variants Expand ..:

Arlabosse, T ; Materna, M ; Riccio, O...
info:eu-repo/semantics/altIdentifier/doi/10.1007/s10875-023-01539-y. , 2023

Link: https://serval.unil.ch/n..

5

Clinical and Molecular Diagnosis of Osteocraniostenosis in ..:

Rosato, S ; Unger, S ; Campos-Xavier, B...
info:eu-repo/semantics/altIdentifier/doi/10.3390/genes13020261. , 2022

Link: https://serval.unil.ch/n..

6

Agenesis of the Corpus Callosum with Facial Dysmorphism and..:

Lebon, S ; Quinodoz, M ; Peter, V.G...
info:eu-repo/semantics/altIdentifier/doi/10.3390/genes12091397. , 2021

Link: https://serval.unil.ch/n..

7

Classical homocystinuria, is it safe to exercise?:

Campos-Xavier, B ; Braissant, O ; Pedro, R.
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ymgmr.2021.100746. , 2021

Link: https://serval.unil.ch/n..

8

Clinical and Genetic Findings in a Series of Eight Families..:

Pollazzon, M ; Caraffi, S.G ; Faccioli, S...
info:eu-repo/semantics/altIdentifier/doi/10.3390/genes13010029. , 2021

Link: https://serval.unil.ch/n..

9

Correction to: Elevated lactate in Mauriac syndrome: still ..:

Touilloux, B ; Lu, H ; Campos-Xavier, B...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s12902-021-00858-8. , 2021

Link: https://serval.unil.ch/n..

10

Osteogenesis imperfecta: towards an individualised interdis..:

Aubry-Rozier, B ; Richard, C ; Unger, S...
info:eu-repo/semantics/altIdentifier/doi/10.4414/smw.2020.20285. , 2020

Link: https://serval.unil.ch/n..

11

Cardiospondylocarpofacial syndrome as a distinct hereditary..:

Salgado, JR ; Pereira, J ; McEntagart, M...
https://openaccess.sgul.ac.uk/id/eprint/111970/1/Cardiospondylocarpofacial%20syndrome%20as%20a%20distinct%20hereditary%20connective%20tissue%20disorder.pdf. , 2020

Link: https://openaccess.sgul...

12

The Connective Tissue Disorder Associated with Recessive Va..:

Kumps, C ; Campos-Xavier, B ; Hilhorst-Hofstee, Y...
info:eu-repo/semantics/altIdentifier/doi/10.3390/genes11040420. , 2020

Link: https://serval.unil.ch/n..

13

Severe Peripheral Joint Laxity is a Distinctive Clinical Fe..:

Caraffi, S.G ; Maini, I ; Ivanovski, I...
info:eu-repo/semantics/altIdentifier/doi/10.3390/genes10100799. , 2019

Link: https://serval.unil.ch/n..

14

The Liberfarb syndrome, a multisystem disorder affecting ey..:

Peter, V.G ; Quinodoz, M ; Pinto-Basto, J...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41436-019-0595-x. , 2019

Link: https://serval.unil.ch/n..

15

Urinary pyridinoline cross-links as biomarkers of osteogene..:

Lindert, U ; Kraenzlin, M ; Campos-Xavier, A.B...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s13023-015-0315-9. , 2015

Link: https://serval.unil.ch/n..