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Showing results (431-440 of 464) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|January 4, 2007
Heterozygous missense mutations in steroidogenic factor 1 (SF1/Ad4BP, NR5A1) are associated with 46,XY disorders of sex development with normal adrenal functionLin Lin, Pascal Philibert, Bruno Ferraz-de-Souza, et al.
Scientific Reports|May 6, 2025
Mapping the anatomical and transcriptional landscape of early human fetal ovary developmentSinead M McGlacken-Byrne, Ignacio Del Valle, Theodoros Xenakis, et al.
Academic Pathology|November 19, 2024
Social media in pathology and laboratory medicine: A systematic reviewAllyson Flippo, Bhakti Dixit, Casey P Schukow, et al.
Journal of Neuroscience Methods|January 19, 2023
Construction of a computerized adaptive test (CAT-CCNB) for efficient neurocognitive and clinical psychopathology assessmentTyler M Moore, Akira Di Sandro, J Cobb Scott, et al.
The Journal of Clinical Endocrinology and Metabolism|August 20, 2010
Health status of adults with congenital adrenal hyperplasia: a cohort study of 203 patientsWiebke Arlt, Debbie S Willis, Sarah H Wild, et al.
Nature Communications|March 30, 2024
A conserved NR5A1-responsive enhancer regulates SRY in testis-determinationDenis Houzelstein, Caroline Eozenou, Carlos F Lagos, et al.
Journal of Geophysical Research. Atmospheres : JGR|August 25, 2020
Atmospheric implications of large C<sub>2</sub>-C<sub>5</sub> alkane emissions from the U.S. oil and gas industryZ A Tzompa-Sosa, B H Henderson, C A Keller, et al.
The Journal of Clinical Endocrinology and Metabolism|January 23, 2013
Genotype-phenotype correlation in 153 adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: analysis of the United Kingdom Congenital adrenal Hyperplasia Adult Study Executive (CaHASE) cohortNils Krone, Ian T Rose, Debbie S Willis, et al.
The Journal of Clinical Endocrinology and Metabolism|February 12, 2005
Analysis of multiple data sets reveals no association between the insulin gene variable number tandem repeat element and polycystic ovary syndrome or related traitsBrenda L Powell, Lema Haddad, Amanda Bennett, et al.
The Journal of Clinical Endocrinology and Metabolism|January 22, 2010
Functional consequences of seven novel mutations in the CYP11B1 gene: four mutations associated with nonclassic and three mutations causing classic 11{beta}-hydroxylase deficiencySilvia Parajes, Lourdes Loidi, Nicole Reisch, et al.
Pageof 47

Showing results (431-440 of 464) with videos related to

Sort By:
Pageof 47
The Journal of Clinical Endocrinology and Metabolism|January 4, 2007
Heterozygous missense mutations in steroidogenic factor 1 (SF1/Ad4BP, NR5A1) are associated with 46,XY disorders of sex development with normal adrenal functionLin Lin, Pascal Philibert, Bruno Ferraz-de-Souza, et al.
Scientific Reports|May 6, 2025
Mapping the anatomical and transcriptional landscape of early human fetal ovary developmentSinead M McGlacken-Byrne, Ignacio Del Valle, Theodoros Xenakis, et al.
Academic Pathology|November 19, 2024
Social media in pathology and laboratory medicine: A systematic reviewAllyson Flippo, Bhakti Dixit, Casey P Schukow, et al.
Journal of Neuroscience Methods|January 19, 2023
Construction of a computerized adaptive test (CAT-CCNB) for efficient neurocognitive and clinical psychopathology assessmentTyler M Moore, Akira Di Sandro, J Cobb Scott, et al.
The Journal of Clinical Endocrinology and Metabolism|August 20, 2010
Health status of adults with congenital adrenal hyperplasia: a cohort study of 203 patientsWiebke Arlt, Debbie S Willis, Sarah H Wild, et al.
Nature Communications|March 30, 2024
A conserved NR5A1-responsive enhancer regulates SRY in testis-determinationDenis Houzelstein, Caroline Eozenou, Carlos F Lagos, et al.
Journal of Geophysical Research. Atmospheres : JGR|August 25, 2020
Atmospheric implications of large C<sub>2</sub>-C<sub>5</sub> alkane emissions from the U.S. oil and gas industryZ A Tzompa-Sosa, B H Henderson, C A Keller, et al.
The Journal of Clinical Endocrinology and Metabolism|January 23, 2013
Genotype-phenotype correlation in 153 adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: analysis of the United Kingdom Congenital adrenal Hyperplasia Adult Study Executive (CaHASE) cohortNils Krone, Ian T Rose, Debbie S Willis, et al.
The Journal of Clinical Endocrinology and Metabolism|February 12, 2005
Analysis of multiple data sets reveals no association between the insulin gene variable number tandem repeat element and polycystic ovary syndrome or related traitsBrenda L Powell, Lema Haddad, Amanda Bennett, et al.
The Journal of Clinical Endocrinology and Metabolism|January 22, 2010
Functional consequences of seven novel mutations in the CYP11B1 gene: four mutations associated with nonclassic and three mutations causing classic 11{beta}-hydroxylase deficiencySilvia Parajes, Lourdes Loidi, Nicole Reisch, et al.
Pageof 47