MEHMO, a novel syndrome: assignment of disease locus to Xp21.1-p22.13. Mental retardation, epileptic seizures, hypogonadism and genitalism, microcephaly, obesity
ContributorsDeLozier-Blanchet, C; Haenggeli, Charles-Antoine; Bottani, Armand
Published inEuropean journal of human genetics, vol. 7, no. 6, p. 621-622
Publication date1999
Keywords
- Abnormalities, Multiple
- Adolescent
- Child, Preschool
- Chromosome Mapping
- Diagnosis, Differential
- Electroencephalography
- Epilepsy/genetics
- Genetic Linkage
- Humans
- Hypogonadism/genetics
- Infant
- Intellectual Disability/genetics
- Male
- Microcephaly/genetics
- Obesity/genetics
- Syndrome
- X Chromosome
Citation (ISO format)
DELOZIER-BLANCHET, C, HAENGGELI, Charles-Antoine, BOTTANI, Armand. MEHMO, a novel syndrome: assignment of disease locus to Xp21.1-p22.13. Mental retardation, epileptic seizures, hypogonadism and genitalism, microcephaly, obesity. In: European journal of human genetics, 1999, vol. 7, n° 6, p. 621–622. doi: 10.1038/sj.ejhg.5200364
Main files (1)
Article (Published version)
Identifiers
- PID : unige:74316
- DOI : 10.1038/sj.ejhg.5200364
- PMID : 10482947
ISSN of the journal1018-4813
