Insight Into the Genetics of Glaucoma
WEDNESDAY, March three, 2021 Scientists have determined 44 new genetic variants connected with glaucoma, a
Genetics
CYLD cutaneous syndrome: MedlinePlus Genetics
CYLD cutaneous syndrome is a genetic condition characterized by the growth of multiple noncancerous (benign)
Genetics Might Explain Some Cases of Cerebral Palsy
THURSDAY, Oct. one, 2020 (HealthDay News) Genetic challenges result in about fourteen% of cerebral palsy
Maturity-onset diabetes of the young – Genetics Home Reference
Maturity-onset diabetes of the young (MODY) is a team of many problems characterized by abnormally
Hailey-Hailey disease – Genetics Home Reference
Behne MJ, Tu CL, Aronchik I, Epstein E, Bench G, Bikle DD, Pozzan T, Mauro
Snijders Blok-Campeau syndrome – Genetics Home Reference
Snijders Blok L, Rousseau J, Twist J, Ehresmann S, Takaku M, Venselaar H, Rodan LH,
Blood Type, Genetics, Odds for COVID-19
By Robin Foster and E.J. MundellHealthDay Reporters THURSDAY, June eighteen, 2020 — A person’s genes
Nonketotic hyperglycinemia – Genetics Home Reference
Aliefendioğlu D, Tana Aslan Ay, Coşkun T, Dursun A, Cakmak FN, Kesimer M. Transient nonketotic
Constitutional mismatch repair deficiency syndrome – Genetics Home Reference
Constitutional mismatch fix deficiency (CMMRD) syndrome is a scarce problem that significantly improves the risk
Saul-Wilson syndrome – Genetics Home Reference
Ferreira CR, Xia ZJ, Clément A, Parry DA, Davids M, Taylan F, Sharma P, Turgeon
ADPEAF – Genetics Home Reference
Autosomal dominant partial epilepsy with auditory features (ADPEAF) is an uncommon form of epilepsy that
STAC3 disorder – Genetics Home Reference
Campiglio M, Flucher BE. STAC3 stably interacts via its C1 domain with Ca(V)one.one in skeletal
Craniofrontonasal syndrome – Genetics Home Reference
Craniofrontonasal syndrome is a uncommon situation characterized by the untimely closure of specified bones of