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Papers of Dr James Harrison Renwick, 1926-1994, geneticist, University of Glasgow, Scotland
Research material
Renwick pedigrees: disease
HC, Huntingdon's chorea
Huntingdon's chorea pedigrees and related data
Printed pedigrees and coding sheets relating to Renwick's linkage study into Huntingdon's chorea
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Printed pedigrees and coding sheets relating to Renwick's linkage study into Huntingdon's chorea
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Bookmark:
http://archiveshub.jisc.ac.uk/data/gb248-ugc155/ugc155/3/3/44/6/7
This material is held at
University of Glasgow Archive Services
Reference
GB 248 UGC 155/3/3/44/6/7
Dates of Creation
1950s-1990s
Physical Description
6 pages
Access Information
RESTRICTED ACCESS.
Please contact the duty archivist to apply for permission to view this material.
Archive Record
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Table of contents
Table of contents
Expanded
Papers of Dr James Harrison Renwick, 1926-1994, geneticist, University of Glasgow, Scotland
UGC 155
Biographical material
UGC 155/1
University of Glasgow material
UGC 155/2
Research material
UGC 155/3
Renwick coding material
UGC 155/3/1
Research methodology
UGC 155/3/2
Renwick pedigrees: disease
UGC 155/3/3
AA, Congenital analgesia
UGC 155/3/3/1
AC, Hereditary spherocytosis
UGC 155/3/3/2
AD, Adynamia episodica
UGC 155/3/3/3
AE, Angioneurotic oedema
UGC 155/3/3/4
AF, Abnormal fibrinogen
UGC 155/3/3/5
AH, Achondroplasia
UGC 155/3/3/6
AN, Aniridia
UGC 155/3/3/7
AO family pedigree
UGC 155/3/3/8
AT1, Ataxia
UGC 155/3/3/9
AT2, Friedreich's Ataxia
UGC 155/3/3/10
File marked Atcania and Actamia regarding Charcot-Marie-Tooth disease
UGC 155/3/3/11
AZ, Alzheimer's Disease
UGC 155/3/3/12
BM, Bloom's Syndrome
UGC 155/3/3/13
BP, Bishop pedigree correspondence
UGC 155/3/3/14
BR, Brachydactyly
UGC 155/3/3/15
CA, Cataracts
UGC 155/3/3/16
CD, Corneal dystrophy
UGC 155/3/3/17
CK, Polycystic kidneys
UGC 155/3/3/18
CL, Caldwell antigen
UGC 155/3/3/19
CO, Co a antigen
UGC 155/3/3/20
CP, Camptodactyly
UGC 155/3/3/21
CT, Catalase
UGC 155/3/3/22
Cardiomyopathy
UGC 155/3/3/23
DA, Diaphysial aclasis (or multiple exostosis)
UGC 155/3/3/24
DE, Deafness
UGC 155/3/3/25
DG, Dermatoglyphic syndromes
UGC 155/3/3/26
DH, Dermatitis herpetiformis
UGC 155/3/3/27
DM, Dystrophia myotonica
UGC 155/3/3/28
DR, pedigrees
UGC 155/3/3/29
DW, Dwarfism
UGC 155/3/3/30
EA, Epithelioma adenoides
UGC 155/3/3/31
EB, Epidermolysis bullosa
UGC 155/3/3/32
EC, Ectrodactyly
UGC 155/3/3/33
EL, Elliptocytosis
UGC 155/3/3/34
EN, En a antigen
UGC 155/3/3/35
EO, Ectronychia
UGC 155/3/3/36
GA, Galactosaemia
UGC 155/3/3/37
GB, Jobbins antigen
UGC 155/3/3/38
GE, Ge antigen
UGC 155/3/3/39
GI, Giant WBC
UGC 155/3/3/40
GL, Renal glycosuria
UGC 155/3/3/41
GO, Gonzalez antigen
UGC 155/3/3/42
HN, Hereditary benign intraepithelial dyskeratosis
UGC 155/3/3/43
HC, Huntingdon's chorea
UGC 155/3/3/44
Huntingdon's chorea literature
UGC 155/3/3/44/1
Huntingdon's chorea graphs
UGC 155/3/3/44/2
Drafts of Linkage and association studies of Huntington's chorea in relation to fifteen genetic markers, by L Beckman, B Cedergren, B Mattson, J O Ottosson and Renwick
UGC 155/3/3/44/3
Correspondence between Renwick and Professor Lars Beckman
UGC 155/3/3/44/4
Graphs and tables of data relating to Professor Lars Beckman's studies into Huntingdon's chorea
UGC 155/3/3/44/5
Huntingdon's chorea pedigrees and related data
UGC 155/3/3/44/6
Article and cuttings relating to Huntingdon's chorea
UGC 155/3/3/44/6/1
Table of data and coding sheets relating to linkage studies of Huntingdon's chorea
UGC 155/3/3/44/6/2
Correspondence concerning patient's with Huntingdon's chorea
UGC 155/3/3/44/6/3
Huntingdon's chorea pedigrees
UGC 155/3/3/44/6/4
Pedigrees, blood test results, correspondence and notes relating to Huntingdon's chorea
UGC 155/3/3/44/6/5
Pedigrees, patient notes, and coding sheets relating to Renwick's linkage study into Huntingdon's chorea
UGC 155/3/3/44/6/6
Printed pedigrees and coding sheets relating to Renwick's linkage study into Huntingdon's chorea
UGC 155/3/3/44/6/7
HE, Haemolytic anaemia
UGC 155/3/3/45
HM, Holt-Oram
UGC 155/3/3/46
HU, Hunter antigen
UGC 155/3/3/47
H22, unidentified disease
UGC 155/3/3/48
H33, unidentified disease
UGC 155/3/3/49
ICB, Bullous ichthyosiform erythroderma
UGC 155/3/3/50
II, unidentified disease
UGC 155/3/3/51
INH, unidentified disease
UGC 155/3/3/52
KA, Kartagener's Syndrome
UGC 155/3/3/53
KN, Koilonychia
UGC 155/3/3/54
LA, Leucocyte antigens
UGC 155/3/3/55
LE, Ectopia lentis
UGC 155/3/3/56
LI, Lipoma draft pedigree chart
UGC 155/3/3/57
LS, Laustia pedigrees
UGC 155/3/3/58
MA, Marfan's Syndrome
UGC 155/3/3/59
MD, Muscular dystrophy
UGC 155/3/3/60
MI, Milroy's Disease
UGC 155/3/3/61
MT, Mt a antigen
UGC 155/3/3/62
MX, Monilethrix
UGC 155/3/3/63
NE, Neurofibromatosis
UGC 155/3/3/64
Correspondence between Renwick, Dr Atef K Sayed, and Dr Robin M Bannerman
UGC 155/3/3/65
Papers on acoustic neuromania
UGC 155/3/3/66
NP, Nail-Patella Syndrome (Hereditary osteo-onycho-dystrophy/dysplasia)
UGC 155/3/3/67
NV, Nevoid basal cell carcinoma
UGC 155/3/3/68
NY, Nystagmus
UGC 155/3/3/69
OA, Optic atrophy
UGC 155/3/3/70
OI, Osteogenesis imperfecta
UGC 155/3/3/71
OP, Oculo-pharyngeal myopathy
UGC 155/3/3/72
OT, Otosclerosis
UGC 155/3/3/73
PA, Pachyonychia
UGC 155/3/3/74
PD, Polydactyly
UGC 155/3/3/75
PE, Pelger-Huet Anomaly
UGC 155/3/3/76
PK(U), Phenylketonuria
UGC 155/3/3/77
PO1, Familial polyposis coli
UGC 155/3/3/78
PO2, Gardner's Syndrome
UGC 155/3/3/79
PR, Pre-auricular sinus
UGC 155/3/3/80
PV, Acro-Pectoro-Vertebral Dysplasia
UGC 155/3/3/81
PX, Xeroderma pigmentosum
UGC 155/3/3/82
PXE, Pseudoxanthoma elasticum
UGC 155/3/3/83
RA, Red cell antigen
UGC 155/3/3/84
RDD, Honeycomb retinal degeneration of Doyne
UGC 155/3/3/85
RDM, Pseudo-inflammatory macular dystrophy
UGC 155/3/3/86
RN, Radicular neuropathy
UGC 155/3/3/87
RP, retinitus pigmentosa
UGC 155/3/3/88
SC, Spastic paraplegia
UGC 155/3/3/89
SF, Symphalangism (Stiff Fingers)
UGC 155/3/3/90
SH, Short palate
UGC 155/3/3/91
SP, Small Patella Syndrome
UGC 155/3/3/92
SW, Swann antigen
UGC 155/3/3/93
SY, Syndactyly with hypertelorism (Mohr's Syndrome)
UGC 155/3/3/94
SZ, unidentified disease
UGC 155/3/3/95
SSE, Self-healing Squamous Epithelioma
UGC 155/3/3/96
TB, Thyroxine binding
UGC 155/3/3/97
TE, Telangiectasia
UGC 155/3/3/98
TF, Transferrin locus
UGC 155/3/3/99
Torkildsen antigen
UGC 155/3/3/100
TP, Triosephosphate isomerase deficiency
UGC 155/3/3/101
TS, Tuberous sclerosis
UGC 155/3/3/102
TY, Tylosis
UGC 155/3/3/103
WA, Waardenburg's Syndrome
UGC 155/3/3/104
WE, antigen Vel
UGC 155/3/3/105
WM, White Mouth (White sponge naevus)
UGC 155/3/3/106
X chromosome-linked main condition
UGC 155/3/3/107
Y pedigree charts
UGC 155/3/3/108
Z pedigree charts
UGC 155/3/3/109
Pedigrees: chromosomal abnormality
UGC 155/3/4
Pedigrees: non-disease
UGC 155/3/5
Logarithm of Odds (LOD)
UGC 155/3/6
Linkage material
UGC 155/3/7
Maps and clusters
UGC 155/3/8
Work of others geneticists
UGC 155/3/9
Miscellaneous genetics research
UGC 155/3/10
Material relating to Renwick's later research interests
UGC 155/3/11
Renwick material relating to the funding of research
UGC 155/3/12
Publications
UGC 155/4
Lectures and conferences
UGC 155/5
Societies and organisations
UGC 155/6
Correspondence files
UGC 155/7