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NARA Subscribed8
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Springer Nature8
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Familial Cancer1
Human Genetics3
Metabolic Brain Disease2
NeuroMolecular Medicine2
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20142
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Rajkumar Ramesar results 8 · Newest (Page 1/1, per page 25)
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Fertility and apparent genetic anticipation in Lynch syndromeNARA Subscribed
Familial Cancer · 2014 · Vol. 13 · Issue 3 · Springer
Douglas Stupart; Aung Ko Win; Mark Jenkins; Ingrid M. Winship; Paul Goldberg; Rajkumar Ramesar
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Haplotype-based study of the association of alcohol and acetaldehyde-metabolising genes with alcohol dependence (with or without comorbid anxiety symptoms) in a Cape Mixed Ancestry populationNARA Subscribed
Metabolic Brain Disease · 2014 · Vol. 29 · Issue 2 · Springer
Andrew Crawford; Shareefa Dalvie; Sarah Lewis; Anthony King; Israel Liberzon; George Fein; Karestan Koenen; Rajkumar Ramesar; Dan J. Stein
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A linkage and family-based association analysis of a potential neurocognitive endophenotype of bipolar disorderNARA Subscribed
NeuroMolecular Medicine · 2007 · Vol. 9 · Issue 2 · Springer
Jonathan Savitz; Lize van der Merwe; Mark Solms; Rajkumar Ramesar
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A linkage and family-based association analysis of a potential neurocognitive endophenotype of bipolar disorderNARA Subscribed
NeuroMolecular Medicine · 2007 · Vol. 9 · Issue 2 · Springer
Jonathan Savitz; Lize Merwe; Mark Solms; Rajkumar Ramesar
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A brain-behaviour initiative for South Africa: the time is rightNARA Subscribed
Metabolic Brain Disease · 2006 · Vol. 21 · Issue 2-3 · Springer
Dan J. Stein; Willie Daniels; Robin Emsley; Brian Harvey; Jonathan Blackburn; Paul Carey; George Ellis; Nicola Illing; Alan Flisher; Hanlie Moolman-Smook; Kelvin Mwaba; Rajkumar Ramesar; Vivienne Russell; Soraya Seedat; Colin Tredoux; Christopher L. Vaughan; Bavanisha Vythilingum; James Warwick
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Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North AmericaNARA Subscribed
Human Genetics · 2001 · Vol. 108 · Issue 1 · Springer
M. Bassi; Arthur Bergen; Pierre Bitoun; Stephen Charles; Maurizio Clementi; Richard Gosselin; Jane Hurst; Richard Lewis; Birgit Lorenz; Thomas Meitinger; Ludwine Messiaen; Rajkumar Ramesar; Andrea Ballabio; M. Schiaffino
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Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutationsNARA Subscribed
Human Genetics · 1998 · Vol. 102 · Issue 5 · Springer
Anita L. DeStefano; L. Adrienne Cupples; Kathleen S. Arnos; J. H. Jr. Asher; Clinton T. Baldwin; Susan Blanton; Melisa L. Carey; Elias O. da Silva; T. B. Friedman; Jacquie Greenberg; Anil K. Lalwani; Aubrey Milunsky; Walter E. Nance; Arti Pandya; Rajkumar S. Ramesar; Andrew P. Read; May Tassabejhi; Edward R. Wilcox; L. A. Farrer
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Retinitis pigmentosa locus on 17q (RP17): fine localization to 17q22 and exclusion of the PDEG and TIMP2 genesNARA Subscribed
Human Genetics · 1997 · Vol. 101 · Issue 1 · Springer
Soraya Bardien; Rajkumar Ramesar; Shomi Bhattacharya; J. Greenberg
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