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You searched for: Author/Creator Martin, HowardLimit your search
- Martin, Howard [remove] 6
- Medical genetics -- Periodicals 4
- 616.042 2
- 616.14205 2
- 616.079 1
- 616.4 1
- AGH, array genome hybridisation -- CNV, copy number variants -- DECIPHER, DatabasE of Chromosomal Imbalance and Phenotype in Humans using Ensembl Resources -- DEI, duplication enrichment index -- FACT, FACT, facilitates chromatin transcription -- FISH, fluorescence in situ hybridisation -- LCR, low copy repeat -- MR, mental retardation -- SNP, single nucleotide polymorphism -- UCSC, University of California at Santa Cruz 1
- AMER1 gene -- FAM123B gene -- mosaic -- osteopathia striata with cranial sclerosis -- WTX gene 1
- Bisulfite sequencing -- FOXP3 -- Methylation -- Next‐generation sequencing -- Regulatory T cell 1
- Clinical genetics -- molecular genetics 1
- Endocrine System Diseases -- Periodicals 1