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American Journal of Human Genetics|October 1, 1996
Genetic homogeneity of autoimmune polyglandular disease type IP Björses, J Aaltonen, A Vikman, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 22, 2009
A survey on Prader-Willi syndrome in the Italian population: prevalence of historical and clinical signsA Crinò, G Di Giorgio, C Livieri, et al.
Human Genetics|January 1, 1981
HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiencyM S Pollack, M I New, G J O'Neill, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1980
Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasiaL S Levine, B Dupont, F Lorenzen, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1981
Genetic and hormonal characterization of cryptic 21-hydroxylase deficiencyL S Levine, B Dupont, F Lorenzen, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|June 7, 2005
Cortical visual areas in monkeys: location, topography, connections, columns, plasticity and cortical dynamicsRicardo Gattass, Sheila Nascimento-Silva, Juliana G M Soares, et al.
Scientific Reports|March 19, 2022
A late Middle Pleistocene Middle Stone Age sequence identified at Wadi Lazalim in southern TunisiaEmanuele Cancellieri, Hedi Bel Hadj Brahim, Jaafar Ben Nasr, et al.
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