Associated Papers
Novel compound heterozygous variants in lectin mannose-binding 2-like gene identified in a Chinese autosomal recessive mental retardation-52 (MRT52) patient with phenotype expansion.
Zhou C et al.
Chinese Medical Journal, 2023
37667433 (PubMed )
Supplement: cm9-136-2107-s002.xls › SHEET
Novel combined insulin-like 3 variations of a single nucleotide in cryptorchidism.
Sinopidis X et al.
Journal of Pediatric Endocrinology & Metabolism : Jpem, 2019
Genetic analysis of the human Insulin-like 3 gene: absence of mutations in a Greek paediatric cohort with testicular maldescent.
Mamoulakis C et al.
Andrologia, 2014
Morphogenetic targets and genetics of undescended testis.
Massart F et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation, 2010
INSL3/RXFP2 signaling in testicular descent.
Feng S et al.
Annals of the New York Academy of Sciences, 2009
Hormonal and genetic control of testicular descent.
Ferlin A et al.
Reproductive Biomedicine Online, 2007
Genetic causes of male infertility.
Ferlin A et al.
Reproductive Toxicology (elmsford, N.y.), 2006
Mutation analysis of INSL3 and GREAT/LGR8 genes in familial cryptorchidism.
Feng S et al.
Urology, 2004
Insulin-like 3 signalling in testicular descent.
Adham IM et al.
International Journal of Andrology, 2004
GREAT/LGR8 is the only receptor for insulin-like 3 peptide.
Bogatcheva NV et al.
Molecular Endocrinology (baltimore, Md.), 2003
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