Letter/Communication
Hypogonadotrophic hypogonadism, short stature, cerebellar ataxia, rod-cone retinal dystrophy, and hypersegmented neutrophils: a novel disorder or a new variant of Boucher-Neuhauser syndrome?
Journal of medical genetics, Vol.40(1), pp.e2-2
01/2003
DOI: 10.1136/jmg.40.1.e2
PMCID: PMC1735249
PMID: 12525550
Abstract
no abstract
Details
- Title: Subtitle
- Hypogonadotrophic hypogonadism, short stature, cerebellar ataxia, rod-cone retinal dystrophy, and hypersegmented neutrophils: a novel disorder or a new variant of Boucher-Neuhauser syndrome?
- Creators
- A-K Jbour - National Centre for Diabetes, Endocrinology and Genetics, Amman, JordanA F Mubaidin - Department of Internal Medicine, King Hussein Medical Centre, Amman, JordanM Till - Department of Ophthalmology, Jordan University Hospital, Amman, JordanH El-Shanti - National Centre for Diabetes, Endocrinology and Genetics, Amman, JordanA Hadidi - Department of Radiology, Jordan University Hospital, Amman, JordanK M Ajlouni - National Centre for Diabetes, Endocrinology and Genetics, Amman, Jordan
- Resource Type
- Letter/Communication
- Publication Details
- Journal of medical genetics, Vol.40(1), pp.e2-2
- DOI
- 10.1136/jmg.40.1.e2
- PMID
- 12525550
- PMCID
- PMC1735249
- NLM abbreviation
- J Med Genet
- ISSN
- 0022-2593
- eISSN
- 1468-6244
- Publisher
- BMJ Publishing Group Ltd
- Language
- English
- Date published
- 01/2003
- Academic Unit
- Stead Family Department of Pediatrics; Medical Genetics and Genomics
- Record Identifier
- 9984353836302771
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