Edwards, J H: Dermatoglyphic Analysis of Female Infant With Congenital Disorder

Date:
1961
Reference:
PENROSE/2/20/16/32
Part of:
L. S. Penrose Papers
  • Archives and manuscripts

About this work

Description

Letters predominantly between J H Edwards, Institute of Child Health, University of Birmingham, and Penrose regarding palm and foot prints of a female infant with a congenital disorder, and karyotype results for the family from blood testing.



Also includes letters between M Fraccaro and Penrose regarding prints of the child, and a copy of a letter from R Wigglesworth to Dr Emanuel, January 1964, about the case.



Also contains palm and hand prints for the family of the patient, drawings of dermal ridge patterns on the hands and feet for three generations of the family, dermatoglyphic and chromosomal analysis reports from the Galton Laboratory, and a karyogram and karyotype for the patient.

Publication/Creation

1961

Physical description

67 folios

Terms of use

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.

Location of duplicates

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

Languages

Where to find it

Location of original

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.

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