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- 2024
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Mark
A genomic mutational constraint map using variation in 76,156 human genomes
(
- Contribution to journal › Article
- 2022
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Mark
Multi-Omic Investigations of a 17-19 Translocation Links MINK1 Disruption to Autism, Epilepsy and Osteoporosis
(
- Contribution to journal › Article
- 2012
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Mark
Characterization of mutations in barley fch2 encoding chlorophyllide a oxygenase
(
- Contribution to journal › Article
- 2008
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Mark
An investigation into whether deletions in 9p reflect prognosis in adult precursor B-cell acute lymphoblastic leukemia : a multi-center study of 381 patients
(
- Contribution to journal › Article
- 2006
-
Mark
Chromosome aberrations including der(6)t(2;6)(p15;p21.3) and der(22)t(3;22)(p21;p11) in the evolution of essential thrombocythemia to myelofibrosis with myeloid metaplasia
(
- Contribution to journal › Article
- 2005
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Mark
Interspecies synteny mapping identifies a quantitative trait locus for bone mineral density on human chromosome Xp22
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- Contribution to journal › Article
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Mark
A manually curated functional annotation of the human X chromosome
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- Contribution to journal › Letter
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Mark
Genetic dissection of neurodegeneration and CNS inflammation
(
- Contribution to journal › Article
- 2004
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Mark
Amplification of chromosome 1 sequences in lipomatous tumors and other sarcomas
(
- Contribution to journal › Article
- 2003
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Mark
Comparative cytogenetic and DNA flow cytometric analysis of 242 primary breast carcinomas
(
- Contribution to journal › Article