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Publications by Bernardo D. Pereira
Novel FGFR1 Mutations in Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism: Evidence for the Involvement of an Alternatively Spliced Isoform
Fertility and Sterility
Gynecology
Reproductive Medicine
Obstetrics
Related publications
Nasal Embryonic LHRH Factor (NELF) Mutations in Patients With Normosmic Hypogonadotropic Hypogonadism and Kallmann Syndrome
Fertility and Sterility
Gynecology
Reproductive Medicine
Obstetrics
The Genetic and Molecular Basis of Idiopathic Hypogonadotropic Hypogonadism
Nature Reviews Endocrinology
Endocrinology
Metabolism
Diabetes
Update on the Genetics of Idiopathic Hypogonadotropic Hypogonadism
JCRPE Journal of Clinical Research in Pediatric Endocrinology
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
Novel Mutation in the Gonadotropin-Releasing Hormone Receptor (GNRHR) Gene in a Patient With Normosmic Isolated Hypogonadotropic Hypogonadism
Arquivos Brasileiros de Endocrinologia & Metabologia
GENETICS IN ENDOCRINOLOGY: Genetic Counseling for Congenital Hypogonadotropic Hypogonadism and Kallmann Syndrome: New Challenges in the Era of Oligogenism and Next-Generation Sequencing
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
Cat Eye Syndrome With Hypogonadotropic Hypogonadism.
Internal Medicine
Internal Medicine
Medicine
Hypogonadotropic Hypogonadism and Cleft Lip and Palate Caused by a Balanced Translocation Producing Haploinsufficiency for FGFR1
Journal of Medical Genetics
Genetics
Alternatively Spliced Caspase-6b Isoform Inhibits the Activation of Caspase-6a
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
An Alternatively Spliced Pit-1 Isoform Altered in Its Ability to Trans-Activate
Nucleic Acids Research
Genetics
