Found: 3
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Human MAMLD1 Gene Variations Seem Not Sufficient to Explain a 46,XY DSD Phenotype.
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- PLoS ONE, 2015, v. 10, n. 11, p. 1, doi. 10.1371/journal.pone.0142831
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- Article
High prevalence of variants in skeletal dysplasia associated genes in individuals with short stature and minor skeletal anomalies.
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- European Journal of Endocrinology, 2021, v. 185, n. 5, p. 691, doi. 10.1530/EJE-21-0557
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- Article
Deficiencia nutricional de yodo en gestantes pertenecientes al distrito sanitario Sierra de Huelva-Andévalo, sur de España.
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- Clinical & Translational Investigation / Revista de Investigación Clínica, 2011, v. 63, n. 5, p. 467
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- Article