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UGC155/3/3/1
AA, Congenital analgesia
Digitised copy available
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UGC155/3/3/2
AC, Hereditary spherocytosis
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UGC155/3/3/3
AD, Adynamia episodica
Digitised copy available
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UGC155/3/3/4
AE, Angioneurotic oedema
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UGC155/3/3/5
AF, Abnormal fibrinogen
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UGC155/3/3/6
AH, Achondroplasia
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UGC155/3/3/7
AN, Aniridia
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UGC155/3/3/8
AO family pedigree
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UGC155/3/3/9
AT1, Ataxia
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UGC155/3/3/10
AT2, Friedreich's Ataxia
Digitised copy available
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UGC155/3/3/11
File marked 'Atcania' and 'Actamia' regarding Charcot-Marie-Tooth disease
Digitised copy available
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UGC155/3/3/12
AZ, Alzheimer's Disease
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UGC155/3/3/13
BM, Bloom's Syndrome
Digitised copy available
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UGC155/3/3/14
BP, Bishop pedigree correspondence
Digitised copy available
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UGC155/3/3/15
BR, Brachydactyly
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UGC155/3/3/16
CA, Cataracts
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UGC155/3/3/17
CD, Corneal dystrophy
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UGC155/3/3/18
CK, Polycystic kidneys
Digitised copy available
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UGC155/3/3/19
CL, Caldwell antigen
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UGC155/3/3/20
CO, Co a antigen
Digitised copy available
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UGC155/3/3/21
CP, Camptodactyly
Digitised copy available
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UGC155/3/3/22
CT, Catalase
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UGC155/3/3/23
Cardiomyopathy
Digitised copy available
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UGC155/3/3/24
DA, Diaphysial aclasis (or multiple exostosis)
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UGC155/3/3/25
DE, Deafness
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UGC155/3/3/26
DG, Dermatoglyphic syndromes
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UGC155/3/3/27
DH, Dermatitis herpetiformis
Digitised copy available
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UGC155/3/3/28
DM, Dystrophia myotonica
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UGC155/3/3/29
DR, pedigrees
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UGC155/3/3/30
DW, Dwarfism
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UGC155/3/3/31
EA, Epithelioma adenoides
Digitised copy available
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UGC155/3/3/32
EB, Epidermolysis bullosa
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UGC155/3/3/33
EC, Ectrodactyly
Digitised copy available
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UGC155/3/3/34
EL, Elliptocytosis
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UGC155/3/3/35
EN, 'En a' antigen
Digitised copy available
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UGC155/3/3/36
EO, Ectronychia
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UGC155/3/3/37
GA, Galactosaemia
Digitised copy available
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UGC155/3/3/38
GB, 'Jobbins' antigen
Digitised copy available
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UGC155/3/3/39
GE, Ge antigen
Digitised copy available
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UGC155/3/3/40
GI, Giant WBC
Digitised copy available
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UGC155/3/3/41
GL, Renal glycosuria
Digitised copy available
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UGC155/3/3/42
GO, Gonzalez antigen
Digitised copy available
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UGC155/3/3/43
HN, Hereditary benign intraepithelial dyskeratosis
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UGC155/3/3/44
HC, Huntingdon's chorea
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UGC155/3/3/45
HE, Haemolytic anaemia
Digitised copy available
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UGC155/3/3/46
HM, 'Holt-Oram'
Digitised copy available
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UGC155/3/3/47
HU, Hunter antigen
Digitised copy available
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UGC155/3/3/48
H22, unidentified disease
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UGC155/3/3/49
H33, unidentified disease
Digitised copy available
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UGC155/3/3/50
ICB, Bullous ichthyosiform erythroderma
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UGC155/3/3/51
II, unidentified disease
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UGC155/3/3/52
INH, unidentified disease
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UGC155/3/3/53
KA, Kartagener's Syndrome
Digitised copy available
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UGC155/3/3/54
KN, Koilonychia
Digitised copy available
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UGC155/3/3/55
LA, Leucocyte antigens
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UGC155/3/3/56
LE, Ectopia lentis
Digitised copy available
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UGC155/3/3/57
LI, Lipoma draft pedigree chart
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UGC155/3/3/58
LS, Laustia pedigrees
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UGC155/3/3/59
MA, Marfan's Syndrome
Digitised copy available
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UGC155/3/3/60
MD, Muscular dystrophy
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UGC155/3/3/61
MI, Milroy's Disease
Digitised copy available
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UGC155/3/3/62
MT, 'Mt a' antigen
Digitised copy available
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UGC155/3/3/63
MX, Monilethrix
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UGC155/3/3/64
NE, Neurofibromatosis
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UGC155/3/3/65
Correspondence between Renwick, Dr Atef K Sayed, and Dr Robin M Bannerman
Digitised copy available
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UGC155/3/3/66
Papers on acoustic neuromania
Digitised copy available
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UGC155/3/3/67
NP, Nail-Patella Syndrome (Hereditary osteo-onycho-dystrophy/dysplasia)
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UGC155/3/3/68
NV, Nevoid basal cell carcinoma
Digitised copy available
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UGC155/3/3/69
NY, Nystagmus
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UGC155/3/3/70
OA, Optic atrophy
Digitised copy available
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UGC155/3/3/71
OI, Osteogenesis imperfecta
Digitised copy available
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UGC155/3/3/72
OP, Oculo-pharyngeal myopathy
Digitised copy available
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UGC155/3/3/73
OT, Otosclerosis
Digitised copy available
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UGC155/3/3/74
PA, Pachyonychia
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UGC155/3/3/75
PD, Polydactyly
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UGC155/3/3/76
PE, Pelger-Huet Anomaly
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UGC155/3/3/77
PK(U), Phenylketonuria
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UGC155/3/3/78
PO1, Familial polyposis coli
Digitised copy available
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UGC155/3/3/79
PO2, Gardner's Syndrome
Digitised copy available
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UGC155/3/3/80
PR, Pre-auricular sinus
Digitised copy available
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UGC155/3/3/81
PV, Acro-Pectoro-Vertebral Dysplasia
Digitised copy available
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UGC155/3/3/82
PX, Xeroderma pigmentosum
Digitised copy available
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UGC155/3/3/83
PXE, Pseudoxanthoma elasticum
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UGC155/3/3/84
RA, Red cell antigen
Digitised copy available
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UGC155/3/3/85
RDD, Honeycomb retinal degeneration of Doyne
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UGC155/3/3/86
RDM, Pseudo-inflammatory macular dystrophy
Digitised copy available
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UGC155/3/3/87
RN, Radicular neuropathy
Digitised copy available
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UGC155/3/3/88
RP, retinitus pigmentosa
Digitised copy available
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UGC155/3/3/89
SC, Spastic paraplegia
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UGC155/3/3/90
SF, Symphalangism (Stiff Fingers)
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UGC155/3/3/91
SH, Short palate
Digitised copy available
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UGC155/3/3/92
SP, Small Patella Syndrome
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UGC155/3/3/93
SW, Swann antigen
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UGC155/3/3/94
SY, Syndactyly with hypertelorism (Mohr's Syndrome)
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UGC155/3/3/95
SZ, unidentified disease
Digitised copy available
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UGC155/3/3/96
SSE, Self-healing Squamous Epithelioma
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UGC155/3/3/97
TB, Thyroxine binding
Digitised copy available
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UGC155/3/3/98
TE, Telangiectasia
Digitised copy available
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UGC155/3/3/99
TF, Transferrin locus
Digitised copy available
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UGC155/3/3/100
Torkildsen antigen
Digitised copy available
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UGC155/3/3/101
TP, Triosephosphate isomerase deficiency
Digitised copy available
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UGC155/3/3/102
TS, Tuberous sclerosis
Digitised copy available
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UGC155/3/3/103
TY, Tylosis
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UGC155/3/3/104
WA, Waardenburg's Syndrome
Digitised copy available
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UGC155/3/3/105
WE, antigen Vel
Digitised copy available
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UGC155/3/3/106
WM, White Mouth (White sponge naevus)
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UGC155/3/3/107
X chromosome-linked main condition
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UGC155/3/3/108
'Y'pedigree charts
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UGC155/3/3/109
'Z'pedigree charts