Results 121 to 130 of about 3,243 (180)

SOX10 Mutation Screening for 117 Patients with Kallmann Syndrome. [PDF]

open access: yesJ Endocr Soc, 2021
Shima H   +10 more
europepmc   +1 more source

Seminal Plasma Lipidomics Profiling to Identify Signatures of Kallmann Syndrome. [PDF]

open access: yesFront Endocrinol (Lausanne), 2021
Li X, Wang X, Li H, Li Y, Guo Y.
europepmc   +1 more source

Kallmann syndrome

open access: yes, 2009
Frank Gaillard   +2 more
openaire   +2 more sources

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]

open access: yesSci Rep, 2023
Ben-Mahmoud A   +18 more
europepmc   +1 more source

Kallmann syndrome and paranoid schizophrenia: a rare combination [PDF]

open access: bronze, 2013
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]

open access: yesEur J Endocrinol, 2021
Iivonen AP   +6 more
europepmc   +1 more source

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