A 4–5/21–22 Chromosomal Translocation Associated with Multiple Congenital Anomalies1
- 1 March 1964
- journal article
- research article
- Published by Wiley in Acta Paediatrica
- Vol. 53 (2), 172-181
- https://doi.org/10.1111/j.1651-2227.1964.tb07224.x
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- A CASE OF TRANSLOCATION 21-22/17-18The Lancet, 1963
- A chromosome anomaly in an infant with a degenerative disease of the central nervous systemThe Journal of Pediatrics, 1963
- TRISOMY-18 SYNDROME DUE TO DE-NOVO TRANSLOCATIONThe Lancet, 1963
- Autosomal trisomy of a group 16–18 chromosomeThe Journal of Pediatrics, 1962
- AUTOSOMAL TRISOMYThe Lancet, 1962
- Familial Langdon Down anomaly with chromosomal fusionAnnals of Human Genetics, 1962
- CHROMOSOME TRANSLOCATION AS A CAUSE OF FAMILIAL MONGOLISMThe Lancet, 1960
- The Significance of One Umbilical ArteryArchives of Disease in Childhood, 1960
- A MONGOL GIRL WITH 46 CHROMOSOMESThe Lancet, 1960
- CHROMOSOME COMPLEMENT IN A MONGOLOID MOTHER, HER CHILD, AND THE CHILD'S FATHERThe Lancet, 1960