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American Journal of Human Genetics|August 1, 1990
Microdissection of the fragile X regionR N MacKinnon, M C Hirst, M V Bell, et al.American Journal of Human Genetics|August 1, 1990
Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell linesG K Suthers, V J Hyland, D F Callen, et al.American Journal of Human Genetics|August 1, 1990
A multivariate method for detecting genetic linkage, with application to a pedigree with an adverse lipoprotein phenotypeC I Amos, R C Elston, G E Bonney, et al.American Journal of Human Genetics|August 1, 1990
Genetic epidemiology of hereditary tyrosinemia in Quebec and in Saguenay-Lac-St-JeanM De Braekeleer, J LarochelleAmerican Journal of Human Genetics|July 23, 2013
Imprinted chromatin around DIRAS3 regulates alternative splicing of GNG12-AS1, a long noncoding RNAMalwina Niemczyk, Yoko Ito, Joanna Huddleston, et al.American Journal of Human Genetics|July 30, 2013
Mutations in ZMYND10, a gene essential for proper axonemal assembly of inner and outer dynein arms in humans and flies, cause primary ciliary dyskinesiaDaniel J Moore, Alexandros Onoufriadis, Amelia Shoemark, et al.American Journal of Human Genetics|November 20, 2012
Recurrent de novo mutations in PACS1 cause defective cranial-neural-crest migration and define a recognizable intellectual-disability syndromeJanneke H M Schuurs-Hoeijmakers, Edwin C Oh, Lisenka E L M Vissers, et al.American Journal of Human Genetics|November 20, 2012
Copy-number disorders are a common cause of congenital kidney malformationsSimone Sanna-Cherchi, Krzysztof Kiryluk, Katelyn E Burgess, et al.American Journal of Human Genetics|May 22, 2012
Cantú syndrome is caused by mutations in ABCC9Bregje W M van Bon, Christian Gilissen, Dorothy K Grange, et al.American Journal of Human Genetics|May 29, 2012
Genome-wide association study identifies candidate genes for male fertility traits in humansGülüm Kosova, Nicole M Scott, Craig Niederberger, et al.Pageof 980