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Rivera‐Pedroza, Carlos I.
6
results:
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Online (6)
Mediatypes
Articles (Online) (5)
OpenAccess-fulltext (1)
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1
FGF9 mutation causes craniosynostosis along with multiple s..:
Rodriguez‐Zabala, Maria
;
Aza‐Carmona, Miriam
;
Rivera‐Pedroza, Carlos I.
...
Human Mutation. 38 (2017) 11 - p. 1471-1476 , 2017
Link:
https://doi.org/10.1002/..
?
2
Early severe scoliosis in a patient with atypical progressi..:
Montané, Lucia Sentchordi
;
Marín, Oliver R.
;
Rivera‐Pedroza, Carlos I.
...
American Journal of Medical Genetics Part A. 170 (2016) 6 - p. 1595-1599 , 2016
Link:
https://doi.org/10.1002/..
?
3
A novel SMARCAL1 missense mutation that affects splicing in..:
Barraza-García, Jimena
;
Rivera-Pedroza, Carlos I.
;
Belinchón, Alberta
...
European Journal of Medical Genetics. 59 (2016) 8 - p. 363-366 , 2016
Link:
https://doi.org/10.1016/..
?
4
Expanding the mutation spectrum in 182 Spanish probands wit..:
Paumard-Hernández, Beatriz
;
Berges-Soria, Julia
;
Barroso, Eva
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4463497/. , 2015
Link:
http://www.ncbi.nlm.nih...
?
5
Identification of the fourth duplication of upstream IHH re..:
Barroso, Eva
;
Berges‐Soria, Julia
;
Benito‐Sanz, Sara
...
American Journal of Medical Genetics Part A. 167 (2015) 4 - p. 902-906 , 2015
Link:
https://doi.org/10.1002/..
?
6
Two novel POC1A mutations in the primordial dwarfism, SOFT ..:
Barraza‐García, Jimena
;
Iván Rivera‐Pedroza, Carlos
;
Salamanca, Luis
...
American Journal of Medical Genetics Part A. 170 (2015) 1 - p. 210-216 , 2015
Link:
https://doi.org/10.1002/..
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