Associated Papers
Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomalies.
Zeidler C et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology, 2014
The results of CHD7 analysis in clinically well-characterized patients with Kallmann syndrome.
Bergman JE et al.
The Journal of Clinical Endocrinology and Metabolism, 2012
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