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Papers of Dr James Harrison Renwick, 1926-1994, geneticist, University of Glasgow, Scotland

Papers of Dr James Harrison Renwick, research material

Renwick pedigrees: disease

Pedigrees, associated data and article on Hereditary ataxia

Pedigrees and associated family data

'Familial peroneal muscular atrophy and its association with the familial ataxias and tremor and longevity' in <i>Journal of Neurology, Neurosurgery and Psychiatry,</i> (1956), 19, 155, by Raymond Herons

AA, Congenital analgesia

AC, Hereditary spherocytosis

AD, Adynamia episodica

AE, Angioneurotic oedema

AF, Abnormal fibrinogen

AH, Achondroplasia

AN, Aniridia

AO family pedigree

AT2, Friedreich's Ataxia

File marked 'Atcania' and 'Actamia' regarding Charcot-Marie-Tooth disease

AZ, Alzheimer's Disease

BM, Bloom's Syndrome

BP, Bishop pedigree correspondence

BR, Brachydactyly

CA, Cataracts

CD, Corneal dystrophy

CK, Polycystic kidneys

CL, Caldwell antigen

CO, Co a antigen

CP, Camptodactyly

CT, Catalase

Cardiomyopathy

DA, Diaphysial aclasis (or multiple exostosis)

DE, Deafness

DG, Dermatoglyphic syndromes

DH, Dermatitis herpetiformis

DM, Dystrophia myotonica

DR, pedigrees

DW, Dwarfism

EA, Epithelioma adenoides

EB, Epidermolysis bullosa

EC, Ectrodactyly

EL, Elliptocytosis

EN, 'En a' antigen

EO, Ectronychia

GA, Galactosaemia

GB, 'Jobbins' antigen

GE, Ge antigen

GI, Giant WBC

GL, Renal glycosuria

GO, Gonzalez antigen

HN, Hereditary benign intraepithelial dyskeratosis

HC, Huntingdon's chorea

HE, Haemolytic anaemia

HM, 'Holt-Oram'

HU, Hunter antigen

H22, unidentified disease

H33, unidentified disease

ICB, Bullous ichthyosiform erythroderma

II, unidentified disease

INH, unidentified disease

KA, Kartagener's Syndrome

KN, Koilonychia

LA, Leucocyte antigens

LE, Ectopia lentis

LI, Lipoma draft pedigree chart

LS, Laustia pedigrees

MA, Marfan's Syndrome

MD, Muscular dystrophy

MI, Milroy's Disease

MT, 'Mt a' antigen

MX, Monilethrix

NE, Neurofibromatosis

Correspondence between Renwick, Dr Atef K Sayed, and Dr Robin M Bannerman

Papers on acoustic neuromania

NP, Nail-Patella Syndrome (Hereditary osteo-onycho-dystrophy/dysplasia)

NV, Nevoid basal cell carcinoma

NY, Nystagmus

OA, Optic atrophy

OI, Osteogenesis imperfecta

OP, Oculo-pharyngeal myopathy

OT, Otosclerosis

PA, Pachyonychia

PD, Polydactyly

PE, Pelger-Huet Anomaly

PK(U), Phenylketonuria

PO1, Familial polyposis coli

PO2, Gardner's Syndrome

PR, Pre-auricular sinus

PV, Acro-Pectoro-Vertebral Dysplasia

PX, Xeroderma pigmentosum

PXE, Pseudoxanthoma elasticum

RA, Red cell antigen

RDD, Honeycomb retinal degeneration of Doyne

RDM, Pseudo-inflammatory macular dystrophy

RN, Radicular neuropathy

RP, retinitus pigmentosa

SC, Spastic paraplegia

SF, Symphalangism (Stiff Fingers)

SH, Short palate

SP, Small Patella Syndrome

SW, Swann antigen

SY, Syndactyly with hypertelorism (Mohr's Syndrome)

SZ, unidentified disease

SSE, Self-healing Squamous Epithelioma

TB, Thyroxine binding

TE, Telangiectasia

TF, Transferrin locus

Torkildsen antigen

TP, Triosephosphate isomerase deficiency

TS, Tuberous sclerosis

TY, Tylosis

WA, Waardenburg's Syndrome

WE, antigen Vel

WM, White Mouth (White sponge naevus)

X chromosome-linked main condition

'Y'pedigree charts

'Z'pedigree charts

AT1, Ataxia

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AT1, Ataxia

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