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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Genetics of Reproductive Disorders (Including Kallmann Syndrome) and Cleft Lip and/or Palate46 XY differences of sex development, Adnexal Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, Cysts, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Genital Diseases, Jaw Abnormalities, Jaw Diseases, Kallmann syndrome, Male Urogenital Diseases, Maxillofacial Abnormalities, Mouth Abnormalities, Musculoskeletal Abnormalities, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, Stomatognathic Diseases, Stomatognathic System Abnormalities, Urogenital Abnormalities, Urogenital Diseases, anosmia, cleft lip, cleft lip/palate, cleft palate, cryptorchidism, disorder of sexual differentiation, endocrine system disorder, female reproductive system disorder, gonadal disorder, hereditary disease, hypogonadism, hypogonadotropic hypogonadism, infertility disorder, lip disorder, male reproductive system disorder, mouth disorder, musculoskeletal system disorder, neoplasm, nervous system disorder, ovarian cyst, ovarian disorder, penile agenesis, polycystic ovary syndrome, precocious puberty, testicular disorderRecruitingNot stated2022-06-21NCT01601171

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Research sitesCityCountryLinked trials
Centre Hospitalier Universitaire Vaudois (CHUV)LausanneSwitzerland15