Results 101 to 110 of about 2,952 (186)
Loss-of-Function Mutations in SOX10 Cause Kallmann Syndrome with Deafness [PDF]
, 2013 Véronique Pingault +19 more
openalex +1 more source
Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome [PDF]
, 2013 Luciana Ribeiro Montenegro +7 more
openalex +1 more source
Olfactory Agenesis in Kallmann Syndrome (KS) [PDF]
Journal of Clinical and Diagnostic Research, 2015 Sahana Shetty +3 more
doaj +1 more source
[Olfactory function and olfactory bulbs in patients with Kallmann syndrome]. [PDF]
Probl Endokrinol (Mosk), 2023 Kokoreva KD +5 more
europepmc +1 more source
Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2
, 2005 Catherine Dodé +17 more
openalex +1 more source
X-linked recessive Kallmann syndrome: A case report. [PDF]
World J Clin Cases, 2022 Zhang P, Fu JY.
europepmc +1 more source
Mutation spectrum of Kallmann syndrome: identification of five novel mutations across ANOS1 and FGFR1. [PDF]
Reprod Biol Endocrinol, 2023 Chu G, Li P, Zhao Q, He R, Zhao Y.
europepmc +1 more source