Publicações

Genetic Diagnosis of X-Linked Dominant Hypophosphatemic Rickets in a Cohort Study: Tubular Reabsorption of Phosphate and 1,25(Oh)(2)D Serum Levels Are Associated with Phex Mutation Type

AuthID
P-002-MKZ

Author(s)

Morey, M

Castro Feijoo, L

Barreiro, J

Cabanas, P

Pombo, M

Gil, M

Bernabeu, I

Diaz Grande, JM

Rey Cordo, L

Ariceta, G

[+9]·

Garcia Minaur, S

Rodriguez, B

Juaristi, S

Garcia Pardos, C

Martinez Peinado, A

Millan, JM

Medeira, A

Moldovan, O

Fernandez, A

Loidi, L

View all authors

Tipo de Documento

Article

Year published

2011

Publicado

in BMC MEDICAL GENETICS, ISSN: 1471-2350

Volume: 12, Número: 1, Páginas: 116 (11)

Indexing

Wos^®

Scopus^®

Crossref^®

Pubmed^®

Google Scholar^®

Metadata
Fontes

Publication Identifiers

DOI: 10.1186/1471-2350-12-116

Pubmed: 21902834

SCOPUS: 2-s2.0-80052570068

Wos: WOS:000295778300001

Source Identifiers

ISSN: 1471-2350

Export Publication Metadata

Lista Marked

Adicionar à lista Marked

Info

At this moment we don't have any links to full text documens.

All authors

Show entries

Search:

Name Order	Nome	Name Order	Nome	Name Order	Nome
1	Morey, M;	2	Castro Feijoo, L;	3	Barreiro, J;
4	Cabanas, P;	5	Pombo, M;	6	Gil, M;
7	Bernabeu, I;	8	Diaz Grande, JM;	9	Rey Cordo, L;
10	Ariceta, G;	11	Rica, I;	12	Nieto, J;
13	Vilalta, R;	14	Martorell, L;	15	Vila Cots, J;
16	Aleixandre, F;	17	Fontalba, A;	18	Soriano Guillen, L;
19	Garcia Sagredo, JM;	20	Garcia Minaur, S;	21	Rodriguez, B;
22	Juaristi, S;	23	Garcia Pardos, C;	24	Martinez Peinado, A;
25	Millan, JM;	26	Medeira, A;	27	Moldovan, O;
28	Fernandez, A;	29	Loidi, L;

Showing 1 to 10 of 10 entries

Genetic Diagnosis of X-Linked Dominant Hypophosphatemic Rickets in a Cohort Study: Tubular Reabsorption of Phosphate and 1,25(Oh)(2)D Serum Levels Are Associated with Phex Mutation Type

Links Úteis

Ajuda

Autenticação Federada (Clique na imagem)

Genetic Diagnosis of X-Linked Dominant Hypophosphatemic Rickets in a Cohort Study: Tubular Reabsorption of Phosphate and 1,25(Oh)(2)D Serum Levels Are Associated with Phex Mutation Type

Links Úteis

Ajuda