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European Journal of Human Genetics : EJHG|January 1, 1996
Pure familial spastic paraplegia: clinical and genetic analysis of nine Belgian pedigreesP De Jonghe, L Krols, A Michalik, et al.
Endocrinology, Diabetes & Metabolism Case Reports|April 5, 2024
Selective peripheral tissue response to high testosterone levels in an infertile woman without virilization signsViviana Ostrovsky, Mira Ulman, Rina Hemi, et al.
STAR Protocols|May 1, 2024
Protocol for phage matching, treatment, and monitoring for compassionate bacteriophage use in non-resolving infectionsHadil Onallah, Ortal Yerushalmy, Ron Braunstein, et al.
Prenatal Diagnosis|October 27, 2019
Prenatal diagnosis and postnatal outcome of anterior urethral anomaliesSharon Perlman, Yael Borovitz, David Ben-Meir, et al.
The Journal of Pediatrics|February 13, 2021
Prediction of Childhood Obesity from Nationwide Health RecordsHagai Rossman, Smadar Shilo, Shiri Barbash-Hazan, et al.
Bio-Protocol|March 3, 2021
Isolation and Characterization of Live Yeast Cells from Ancient Clay VesselsTzemach Aouizerat, Aren M Maeir, Yitzhak Paz, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 17, 2015
Two different patterns of mini-puberty in two 46,XY newborns with 17β-hydroxysteroid dehydrogenase type 3 deficiencyKorcan Demir, Melek Yıldız, Özlem Nalbantoğlu Elmas, et al.
Frontiers in Genetics|July 11, 2022
A Null Mutation of <i>TNFRSF11A</i> Causes Dysosteosclerosis, Not OsteopetrosisTarık Kırkgöz, Behzat Özkan, Filiz Hazan, et al.
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