Clinical Assessment and Mutation Analysis of Kallmann Syndrome 1 (<i>KAL1</i>) and Fibroblast Growth Factor Receptor 1 (<i>FGFR1</i>, or<i>KAL2</i>) in Five Families and 18 Sporadic PatientsNaoko Sato, Tsutomu Ogata, Masayo Kagami et al.|The Journal of Clinical Endocrinology & Metabolism|2004Cited by 220
Molecular cloning and mapping of 10 new probes on the human Y chromosomeYutaka Nakahori, Yasuo Nakagome, Motoyasu Kusano et al.|Genomics|1991Cited by 37