A biastellited marker chromosome in an infant with the caudal regression anomalad
- 1 February 1981
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 19 (2) , 126-129
- https://doi.org/10.1111/j.1399-0004.1981.tb00682.x
Abstract
An infant with the caudal regression anomalad is described. Karyotypic analysis revealed mosaicism for a bisatellited microchromosome. Using banding techniques, an attempt was made to further identify the marker chromosome. It is suggested that a causal relationship exists between the cytogenetic findings and the clinical observations.Keywords
This publication has 15 references indexed in Scilit:
- Trisomy 22 in a newborn girl with multiple malformationsHereditas, 2009
- C-bands in seven cases of accessory small chromosomesClinical Genetics, 2008
- Malformation syndrome associated with small extra chromosomeAmerican Journal of Medical Genetics, 1980
- Cat Eye SyndromeAmerican Journal of Diseases of Children, 1977
- A bisatellited marker chromosome in a mentally retarded girl with infantile autismHereditas, 1976
- Bisatellited extra small metacentric chromosome in newbornsClinical Genetics, 1974
- Cat-eye syndrome, a partial trisomy 22Human Genetics, 1972
- A monopodal sireniform monster with dermatoglyphic and cytogenetic studies.Journal of Medical Genetics, 1966
- Potter's SyndromeAmerican Journal of Diseases of Children, 1965
- From the Mermaid to Anal Imperforation: The Syndrome of Caudal RegressionArchives of Disease in Childhood, 1961