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American Journal of Human Genetics|August 27, 2004
Sequence-based linkage analysisItay Furman, Mark J Rieder, Suzanne Da Ponte, et al.American Journal of Human Genetics|June 9, 2004
Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardationPatrick Tarpey, Josep Parnau, Matthew Blow, et al.American Journal of Human Genetics|June 9, 2004
Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35Mary L Marazita, Jeffrey C Murray, Andrew C Lidral, et al.American Journal of Human Genetics|August 11, 2004
Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility regionP Paschou, Y Feng, A J Pakstis, et al.American Journal of Human Genetics|July 17, 2004
High frequency of mosaicism among patients with neurofibromatosis type 1 (NF1) with microdeletions caused by somatic recombination of the JJAZ1 geneH Kehrer-Sawatzki, L Kluwe, C Sandig, et al.American Journal of Human Genetics|July 24, 2004
A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD StudyElizabeth R Hauser, David C Crossman, Christopher B Granger, et al.American Journal of Human Genetics|August 13, 2004
A susceptibility locus for myopia in the normal population is linked to the PAX6 gene region on chromosome 11: a genomewide scan of dizygotic twinsChristopher J Hammond, Toby Andrew, Ying Tat Mak, et al.American Journal of Human Genetics|September 1, 1992
Selection bias in genetic-epidemiological studies of cleft lip and palateK Christensen, N V Holm, J Olsen, et al.American Journal of Human Genetics|May 12, 2004
Hypergonadotropic ovarian failure associated with an inherited mutation of human bone morphogenetic protein-15 (BMP15) geneElisa Di Pasquale, Paolo Beck-Peccoz, Luca PersaniAmerican Journal of Human Genetics|May 27, 2004
Mutations in the FTSJ1 gene coding for a novel S-adenosylmethionine-binding protein cause nonsyndromic X-linked mental retardationKristine Freude, Kirsten Hoffmann, Lars-Riff Jensen, et al.Pageof 979