SOX10 Mutation Screening for 117 Patients with Kallmann Syndrome. [PDF]
Shima H +10 more
europepmc +1 more source
Two cases of Kallmann syndrome caused by a novel mutation in ANOS1: A case report. [PDF]
Xiong JK, Tu SK, Shi M, Song K, Li M.
europepmc +1 more source
Seminal Plasma Lipidomics Profiling to Identify Signatures of Kallmann Syndrome. [PDF]
Li X, Wang X, Li H, Li Y, Guo Y.
europepmc +1 more source
Advances in Genetic Diagnosis of Kallmann Syndrome and Genetic Interruption. [PDF]
Liu Y, Zhi X.
europepmc +1 more source
An Effective Outcome Despite Delayed Treatment Initiation in a Female With Kallmann Syndrome: A Case Report. [PDF]
Taniguchi K +4 more
europepmc +1 more source
A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome. [PDF]
Ben-Mahmoud A +18 more
europepmc +1 more source
Kallmann syndrome and paranoid schizophrenia: a rare combination [PDF]
W.M.A. Verhoeven +3 more
openalex +1 more source
Kallmann syndrome in a patient with Weiss-Kruszka syndrome and a de novo deletion in 9q31.2. [PDF]
Iivonen AP +6 more
europepmc +1 more source

