Roberts syndrome: clinical and cytogenetic aspects
- 1 April 1982
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 19 (2) , 116-119
- https://doi.org/10.1136/jmg.19.2.116
Abstract
A newborn female with intrauterine growth retardation, bilateral cleft lip and palate, absent external nares and eyelids, low set ears, short contracted limbs, webbed digits, intestinal malrotation, and unilateral renal agenesis is reported. These multiple malformations are considered part of the Neu-Laxova syndrome.This publication has 8 references indexed in Scilit:
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- Genetic counselling: the one-in-four risk of a rare disease.1980
- Roberts's syndrome and clonidine.Journal of Medical Genetics, 1979
- Roberts' syndrome.I. Cytological evidence for a disturbance in chromatid pairingClinical Genetics, 1979
- The SC phocomelia and the Roberts syndrome: Nosologic aspectsEuropean Journal of Nuclear Medicine and Molecular Imaging, 1977
- A SIBSHIP WITH THE PSEUDOTHALIDOMIDE SYNDROME AND AN ASSOCIATION WITH Rh INCOMPATIBILITYThe Medical Journal of Australia, 1973
- Familial holoprosencephaly with endocrine dysgenesisThe Journal of Pediatrics, 1968