Edwards, J H: Dermatoglyphic Analysis of Male Infant With Chromosomal Anomaly

Letters between J H Edwards, Institute of Child Health, University of Birmingham, and Penrose regarding a chromosomal anomaly in a male infant, and dermatoglyphic testing on the family. Encloses hand and foot prints from the patient and his parents, drawings of dermal ridge patterns for the family, a chromosome analysis from the Galton Laboratory, and two photographs of the patient.

Sep 1962 - Jul 1964

45 folios

This material contains sensitive personal data. Access to this material will not be granted until after the last date of closure, unless written permission is given by the individual(s) concerned. Closed until 1 January 2064.

A digitised copy is held by the Wellcome Library as part of Codebreakers: Makers of Modern Genetics.

The original material is held at UCL Special Collections. This catalogue is held by the Wellcome Library as part of Codebreakers: Makers of Modern Genetics.