- Title: Subtitle
- Split hand/split foot malformation associated with sensorineural deafness, inner and middle ear malformation, hypodontia, congenital vertical talus, and deletion of eight microsatellite markers in 7q21.1-q21.3
- Creators
- Edda HaberlandtJudith LöfflerAlmut Hirst-StadlmannBernd StöcklWerner JudmaierHelmut FischerPeter Heinz-ErianThomas MüllerGerd UtermannRichard J H SmithAndreas R Janecke
- Resource Type
- Letter/Communication
- Publication Details
- Journal of medical genetics, Vol.38(6), pp.405-409
- DOI
- 10.1136/jmg.38.6.405
- PMID
- 11424924
- PMCID
- PMC1734906
- NLM abbreviation
- J Med Genet
- ISSN
- 0022-2593
- eISSN
- 1468-6244
- Language
- English
- Date published
- 06/2001
- Academic Unit
- Roy J. Carver Department of Biomedical Engineering; Molecular Physiology and Biophysics; Anatomy and Cell Biology; Stead Family Department of Pediatrics; Iowa Neuroscience Institute; Otolaryngology; Internal Medicine
- Record Identifier
- 9984006319202771
Letter/Communication
Split hand/split foot malformation associated with sensorineural deafness, inner and middle ear malformation, hypodontia, congenital vertical talus, and deletion of eight microsatellite markers in 7q21.1-q21.3
Journal of medical genetics, Vol.38(6), pp.405-409
06/2001
DOI: 10.1136/jmg.38.6.405
PMCID: PMC1734906
PMID: 11424924
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