Familial transmission of 16p trisomy in an infant
- 1 January 1989
- journal article
- case report
- Published by Springer Nature in Human Genetics
- Vol. 81 (2) , 196-198
- https://doi.org/10.1007/bf00293904
Abstract
Based on four reported cases including the present case, 16p trisomic infants have remarkably similar features. These are severe developmental delay, psychomotor retardation, typical facies, and anomalies of extremities.Keywords
This publication has 9 references indexed in Scilit:
- Segregation analysis in reciprocal translocation carriersAmerican Journal of Medical Genetics, 1984
- Duplication of 16p from insertion of 16p into 16q with subsequent duplication due to crossing over within the inserted segmentAmerican Journal of Medical Genetics, 1983
- ["De novo" partial trisomy 16p (author's transl)].1981
- Five familial cases with a trisomy 16p syndrome due to translocationClinical Genetics, 1979
- DENOVO TRISOMY-16Q11-]PTER1979
- ‘De novo’ trisomy 16q11→pterHuman Genetics, 1979
- Trisomy 16p in a liveborn infant and a review of partial and full trisomy 16.Journal of Medical Genetics, 1978
- Partial trisomy 16q-Human Genetics, 1977
- Chromosome anomalies as a cause of spontaneous abortionAmerican Journal of Obstetrics and Gynecology, 1967