Results
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1841.
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1842.
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1843.
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1844.
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1845.
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The frequency and the effects of 21-hydroxylase gene defects in congenital adrenal hyperplasia patients. [electronic resource] by
- Kirac, Deniz
- Guney, Ahmet Ilter
- Akcay, Teoman
- Guran, Tulay
- Ulucan, Korkut
- Turan, Serap
- Ergec, Deniz
- Koc, Gulsah
- Eren, Fatih
- Kaspar, Elif Cigdem
- Bereket, Abdullah
Producer: 20151112
In:
Annals of human genetics vol. 78
Availability: No items available.
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1851.
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1852.
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High variability in CYP21A2 mutated alleles in Spanish 21-hydroxylase deficiency patients, six novel mutations and a founder effect. [electronic resource] by
- Loidi, Lourdes
- Quinteiro, Celsa
- Parajes, Silvia
- Barreiro, Jesús
- Lestón, Domingo G
- Cabezas-Agrícola, José M
- Sueiro, Aurelio M
- Araujo-Vilar, David
- Catro-Feijóo, Lidia
- Costas, Javier
- Pombo, Manuel
- Domínguez, Fernando
Producer: 20060721
In:
Clinical endocrinology vol. 64
Availability: No items available.
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1853.
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1854.
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1855.
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De novo intrachromosomal gene conversion from OPN1MW to OPN1LW in the male germline results in Blue Cone Monochromacy. [electronic resource] by
- Buena-Atienza, Elena
- Rüther, Klaus
- Baumann, Britta
- Bergholz, Richard
- Birch, David
- De Baere, Elfride
- Dollfus, Helene
- Greally, Marie T
- Gustavsson, Peter
- Hamel, Christian P
- Heckenlively, John R
- Leroy, Bart P
- Plomp, Astrid S
- Pott, Jan Willem R
- Rose, Katherine
- Rosenberg, Thomas
- Stark, Zornitza
- Verheij, Joke B G M
- Weleber, Richard
- Zobor, Ditta
- Weisschuh, Nicole
- Kohl, Susanne
- Wissinger, Bernd
Producer: 20180424
In:
Scientific reports vol. 6
Availability: No items available.
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