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Ophthalmic Research|September 30, 2005
Exclusion of four candidate genes, KHDRBS2, PTP4A1, KIAA1411 and OGFRL1, as causative of autosomal recessive retinitis pigmentosaMai M Abd El-Aziz, Reshma J Patel, Mohamed F El-Ashry, et al.
Journal of Experimental & Clinical Cancer Research : CR|March 6, 2002
Boron compounds against human leukemic cellsN Murmu, S Mitra, M Das, et al.
Tropical and Geographical Medicine|March 1, 1986
Density of Culex vishnui and appearance of JE antibody in sentinel chicks and wild birds in relation to Japanese encephalitis casesS Bhattacharya, S K Chakraborty, S Chakraborty, et al.
Human Reproduction Open|February 28, 2022
Trends in research on pain relief during oocyte retrieval for IVF/ICSI: a systematic, methodological reviewE T I A Buisman, H Grens, R Wang, et al.
American Journal of Human Genetics|October 1, 1987
Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14A F Wright, S S Bhattacharya, J F Clayton, et al.
Human Molecular Genetics|January 4, 2001
The destabilization of human GCAP1 by a proline to leucine mutation might cause cone-rod dystrophyR J Newbold, E C Deery, C E Walker, et al.
Human Reproduction (Oxford, England)|February 21, 2012
Assisted reproductive technology in Europe, 2007: results generated from European registers by ESHREJ de Mouzon, V Goossens, S Bhattacharya, et al.
Genomics|September 1, 1995
cDNA sequence and gene locus of the human retinal phosphoinositide-specific phospholipase-C beta 4 (PLCB4)R A Alvarez, A J Ghalayini, P Xu, et al.
Human Reproduction (Oxford, England)|June 24, 2010
Assisted reproductive technology in Europe, 2006: results generated from European registers by ESHREJ de Mouzon, V Goossens, S Bhattacharya, et al.
Human Molecular Genetics|July 1, 1996
The gene responsible for autosomal dominant Doyne's honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16C Y Gregory, K Evans, S D Wijesuriya, et al.
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