Related Experiment Videos
[Genetic aspects of the adrenogenital syndrome]
Minerva Endocrinologica
|April 1, 1987
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
In an elite cross of maize a major quantitative trait locus controls one-fourth of the genetic variation for grain yield.
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik·2013
Prenatal features of Noonan syndrome: prevalence and prognostic value.
Prenatal diagnosis·2011
Eyebrow anomalies as a diagnostic sign of genomic disorders.
Clinical genetics·2010
Expanding CEP290 mutational spectrum in ciliopathies.
American journal of medical genetics. Part A·2009
Mowat-Wilson syndrome: facial phenotype changing with age: study of 19 Italian patients and review of the literature.
American journal of medical genetics. Part A·2009
Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients.
Journal of medical genetics·2007
Polycystic ovary syndrome, amenorrhea and the diagnostic role of anti-Müllerian hormone.
Minerva endocrinologica·2021
Effects of Mediterranean diet on semen parameters in healthy young adults: a randomized controlled trial.
Minerva endocrinologica·2021
Codon bias analyses on thyroid carcinoma genes.
Minerva endocrinologica·2020
The possible role of endocrine dysfunction of adipose tissue in gestational diabetes mellitus.
Minerva endocrinologica·2020
Male hypogonadism: therapeutic choices and pharmacological management.
Minerva endocrinologica·2020
Homozygous variants in ZSWIM6 cause severe syndromic short stature and developmental delay.
Hormone research in paediatrics·2026
Before hormones: early sex-specific mechanisms shaping nervous system development, function, and postnatal disease susceptibility.
Frontiers in behavioral neuroscience·2026
The genome sequence of the Silver Colonel, Odontomyia argentata (Fabricius, 1794) (Diptera: Stratiomyidae).
Wellcome open research·2026
The genome sequence of a nematode, Thelazia callipaeda Railliet & Henry, 1910 (Rhabditida: Thelaziidae).
Wellcome open research·2026
Long-read sequencing resolves complex CYP21A2 variants and identifies 2+0 carriers in 21-hydroxylase deficiency.
The Journal of molecular diagnostics : JMD·2026