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Serum leptin level is a regulator of bone mass F Elefteriou, S Takeda, K Ebihara, J Magre, N Patano, C Ae Kim, Y Ogawa, ... Proceedings of the National Academy of Sciences 101 (9), 3258-3263, 2004 | 432 | 2004 |
Congenital abnormalities in Brazilian children associated with misoprostol misuse in first trimester of pregnancy CH Gonzalez, MJ Marques-Dias, CA Kim, SMM Sugayama, JA Da Paz, ... The Lancet 351 (9116), 1624-1627, 1998 | 382 | 1998 |
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Mutations in SRCAP, encoding SNF2-related CREBBP activator protein, cause Floating-Harbor syndrome RL Hood, MA Lines, SM Nikkel, J Schwartzentruber, C Beaulieu, ... The American Journal of Human Genetics 90 (2), 308-313, 2012 | 202 | 2012 |
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Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects LA Mavrogiannis, I Antonopoulou, A Baxová, S Kutílek, CA Kim, ... Nature genetics 27 (1), 17-18, 2001 | 158 | 2001 |
Genomic imbalances associated with müllerian aplasia C Cheroki, ACV Krepischi-Santos, K Szuhai, V Brenner, CAE Kim, PA Otto, ... Journal of medical genetics 45 (4), 228-232, 2008 | 155 | 2008 |
A molecular and clinical study of Larsen syndrome caused by mutations in FLNB LS Bicknell, C Farrington-Rock, Y Shafeghati, P Rump, Y Alanay, ... Journal of medical genetics 44 (2), 89-98, 2007 | 152 | 2007 |
Mechanisms of ring chromosome formation, ring instability and clinical consequences RS Guilherme, VF Ayres Meloni, CA Kim, R Pellegrino, SS Takeno, ... BMC medical genetics 12, 1-7, 2011 | 150 | 2011 |
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