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Genomics|October 1, 1992
Exclusion of linkage between hypokalemic periodic paralysis (HOKPP) and three candidate lociW L Casley, M Allon, H K Cousin, et al.Cell|July 9, 2019
VEGAS as a Platform for Facile Directed Evolution in Mammalian CellsJustin G English, Reid H J Olsen, Katherine Lansu, et al.Iscience|August 30, 2022
Behavioral variation across the days and lives of honey beesMichael L Smith, Jacob D Davidson, Benjamin Wild, et al.American Journal of Medical Genetics|June 8, 2001
Exclusion of linkage to the CDL1 gene region on chromosome 3q26.3 in some familial cases of Cornelia de Lange syndromeI D Krantz, E Tonkin, M Smith, et al.Mechanisms of Development|September 24, 1999
Expression of steroidogenic factor 1 and Wilms' tumour 1 during early human gonadal development and sex determinationN A Hanley, S G Ball, M Clement-Jones, et al.Developmental Dynamics : an Official Publication of the American Association of Anatomists|October 1, 2003
Major role of BAX in apoptosis during retinal development and in establishment of a functional postnatal retinaM O Péquignot, A C Provost, S Sallé, et al.The Journal of Biological Chemistry|March 30, 2001
New splicing-site mutations in the SURF1 gene in Leigh syndrome patientsM O Pequignot, I Desguerre, R Dey, et al.American Journal of Human Genetics|September 22, 2001
Syndromic short stature in patients with a germline mutation in the LIM homeobox LHX4K Machinis, J Pantel, I Netchine, et al.Human Mutation|April 11, 2001
Mutation analysis of the tyrosinase gene in oculocutaneous albinismO Camand, D Marchant, S Boutboul, et al.Journal of Dairy Science|March 31, 2023
Amplifying local serotonin signaling prior to dry-off hastens mammary gland involution and redevelopment in dairy cowsS L Field, B D Davidson, A F Hoerl, et al.Pageof 96