Holt–Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12q - Concepedia

Concepedia

Publication | Closed Access

Holt–Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12q

89

Citations

14

References

1994

Year

Jonathan Terrett, Ruth Newbury‐Ecob, Gareth Cross, Iain Fenton, J. A. Raeburn, I D Young, J. David Brook

Nature Genetics

Genetic DisorderGeneticsLocus MappingPathologyHuman Chromosome 12QMolecular GeneticsHolt–oram SyndromeDisease Gene IdentificationMedicineChromosome 9Clinical Genetics

References

	Year	Citations

Page 1

Page 1