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Best Practice & Research: Clinical Endocrinology & Metabolism, ISSN 1521-690X, 2009, Volume 24, Issue 2, pp. 163 - 186
The process of sexual differentiation is central for reproduction of almost all metazoan, and therefore, for maintenance of practically all multicellular... 
Endocrinology & Metabolism | sex differentiation | ovary | disorders of sex development (DSD) | bipotential state | sex development | testis | sex determination | Life Sciences & Biomedicine | Science & Technology | Gonads - embryology | Sexual Development - genetics | Humans | Intramolecular Oxidoreductases - physiology | DAX-1 Orphan Nuclear Receptor - genetics | Male | Forkhead Transcription Factors - physiology | X-linked Nuclear Protein | Repressor Proteins - physiology | Anti-Mullerian Hormone - genetics | Hedgehog Proteins - genetics | SOXB1 Transcription Factors - genetics | Lipocalins - physiology | Female | SOXB1 Transcription Factors - physiology | Disorders of Sex Development - physiopathology | Nuclear Proteins - genetics | DNA Helicases - genetics | WT1 Proteins - genetics | Forkhead Box Protein L2 | DNA-Binding Proteins - physiology | Transcription Factors - physiology | DAX-1 Orphan Nuclear Receptor - physiology | Gonadal Dysgenesis - genetics | Sex Differentiation - genetics | Polycomb-Group Proteins | Transcription Factors - genetics | Disorders of Sex Development - genetics | Anti-Mullerian Hormone - physiology | Steroidogenic Factor 1 - physiology | Homeodomain Proteins - genetics | GATA4 Transcription Factor - physiology | WT1 Proteins - physiology | Sex Differentiation - physiology | Phenotype | Animals | PAX2 Transcription Factor - physiology | Sexual Development - physiology | LIM-Homeodomain Proteins | Nuclear Proteins - physiology | Wnt Proteins - physiology | Homeodomain Proteins - physiology | Wnt4 Protein | Bone morphogenetic proteins | Development and progression | Genetic disorders | Mental illness | Analysis | Index Medicus
Journal Article
Diabetes (New York, N.Y.), ISSN 1939-327X, 07/2002, Volume 51, Issue 7, pp. 2301 - 2305
Loss of Kinase Activity in a Patient With Wolcott-Rallison Syndrome Caused By a Novel Mutation in the EIF2AK3 Gene Anna Biason-Lauber , Mariarosaria Lang-Muritano , Tindara Vaccaro and Eugen J... 
Life Sciences & Biomedicine | Endocrinology & Metabolism | Science & Technology | Pedigree | Base Sequence | Humans | Polymerase Chain Reaction | Pancreas - pathology | Female | Infant | Male | Mutation | Abnormalities, Multiple - genetics | eIF-2 Kinase - genetics | Genetic aspects | Genetic disorders | Research | Type 1 diabetes | Complications | Diabetes in children | Index Medicus | Abridged Index Medicus
Journal Article
Scientific reports, ISSN 2045-2322, 11/2019, Volume 9, Issue 1, pp. 17033 - 18
Journal Article
Molecular endocrinology (Baltimore, Md.), ISSN 1944-9917, 02/2015, Volume 29, Issue 2, pp. 247 - 257
Journal Article