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Up a levelGroup by: Author | Type
Number of items: 4.
A
Andoniadou, CL;
Signore, M;
Sajedi, E;
Gaston-Massuet, C;
Kelberman, D;
Burns, AJ;
Itasaki, N;
... Martinez-Barbera, JP; + view all
(2007)
Lack of the murine homeobox gene Hesx1 leads to a posterior transformation of the anterior forebrain.
DEVELOPMENT
, 134
(8)
1499 - 1508.
10.1242/dev.02829.
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L
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Lin, L;
Hindmarsh, PC;
Metherell, LA;
Alzyoud, M;
Al-Ali, M;
Brain, CE;
Clark, AJL;
... Achermann, JC; + view all
(2007)
Severe loss-of-function mutations in the adrenocorticotropin receptor (ACTHR, MC2R) can be found in patients diagnosed with salt-losing adrenal hypoplasia.
Clinical Endocrinology
, 66
(2)
205 - 210.
10.1111/j.1365-2265.2006.02709.x.
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Lin, L;
Philibert, P;
Ferraz-de-Souza, B;
Kelberman, D;
Homfray, T;
Albanese, A;
Molini, V;
... Achermann, JC; + view all
(2007)
Heterozygous missense mutations in steroidogenic factor 1 (SF1/Ad4BP, NR5A1) are associated with 46,XY disorders of sex development with normal adrenal function.
The Journal of Clinical Endocrinology & Metabolism
, 92
(3)
991 - 999.
10.1210/jc.2006-1672.
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R
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Runne, H;
Kuhn, A;
Wild, EJ;
Pratyaksha, W;
Kristiansen, M;
Isaacs, JD;
Regulier, E;
... Luthi-Carter, R; + view all
(2007)
Analysis of potential transcriptomic biomarkers for Huntington's disease in peripheral blood.
Proceedings of the National Academy of Sciences
, 104
(36)
14424 - 14429.
10.1073/pnas.0703652104.
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