AF, Abnormal fibrinogen

Archive Unit

For more information, email the repository
Advice on accessing these materials
Cite this description
Bookmark:https://archiveshub.jisc.ac.uk/data/gb248-ugc155/ugc155/3/3/5

This material is held at
Reference
Dates of Creation
Physical Description

Scope and Content

Includes family pedigrees and typing data and a letter from Dr Wilma B Bias asking Renwick to put the data "through the system".

Access Information

RESTRICTED ACCESS.

Please contact the duty archivist to apply for permission to view this material.

Personal Names

Bias, Wilma B, fl 1970s,

Archive Record|Table of contents

Papers of Dr James Harrison Renwick, 1926-1994, geneticist, University of Glasgow, ScotlandUGC 155

Biographical materialUGC 155/1

University of Glasgow materialUGC 155/2

Research materialUGC 155/3

Renwick coding materialUGC 155/3/1

Research methodologyUGC 155/3/2

Renwick pedigrees: diseaseUGC 155/3/3

AA, Congenital analgesiaUGC 155/3/3/1

AC, Hereditary spherocytosisUGC 155/3/3/2

AD, Adynamia episodicaUGC 155/3/3/3

AE, Angioneurotic oedemaUGC 155/3/3/4

AF, Abnormal fibrinogenUGC 155/3/3/5

AH, AchondroplasiaUGC 155/3/3/6

AN, AniridiaUGC 155/3/3/7

AO family pedigreeUGC 155/3/3/8

AT1, AtaxiaUGC 155/3/3/9

AT2, Friedreich's AtaxiaUGC 155/3/3/10

File marked Atcania and Actamia regarding Charcot-Marie-Tooth diseaseUGC 155/3/3/11

AZ, Alzheimer's DiseaseUGC 155/3/3/12

BM, Bloom's SyndromeUGC 155/3/3/13

BP, Bishop pedigree correspondenceUGC 155/3/3/14

BR, BrachydactylyUGC 155/3/3/15

CA, CataractsUGC 155/3/3/16

CD, Corneal dystrophyUGC 155/3/3/17

CK, Polycystic kidneysUGC 155/3/3/18

CL, Caldwell antigenUGC 155/3/3/19

CO, Co a antigenUGC 155/3/3/20

CP, CamptodactylyUGC 155/3/3/21

CT, CatalaseUGC 155/3/3/22

CardiomyopathyUGC 155/3/3/23

DA, Diaphysial aclasis (or multiple exostosis)UGC 155/3/3/24

DE, DeafnessUGC 155/3/3/25

DG, Dermatoglyphic syndromesUGC 155/3/3/26

DH, Dermatitis herpetiformisUGC 155/3/3/27

DM, Dystrophia myotonicaUGC 155/3/3/28

DR, pedigreesUGC 155/3/3/29

DW, DwarfismUGC 155/3/3/30

EA, Epithelioma adenoidesUGC 155/3/3/31

EB, Epidermolysis bullosaUGC 155/3/3/32

EC, EctrodactylyUGC 155/3/3/33

EL, ElliptocytosisUGC 155/3/3/34

EN, En a antigenUGC 155/3/3/35

EO, EctronychiaUGC 155/3/3/36

GA, GalactosaemiaUGC 155/3/3/37

GB, Jobbins antigenUGC 155/3/3/38

GE, Ge antigenUGC 155/3/3/39

GI, Giant WBCUGC 155/3/3/40

GL, Renal glycosuriaUGC 155/3/3/41

GO, Gonzalez antigenUGC 155/3/3/42

HN, Hereditary benign intraepithelial dyskeratosisUGC 155/3/3/43

HC, Huntingdon's choreaUGC 155/3/3/44

HE, Haemolytic anaemiaUGC 155/3/3/45

HM, Holt-OramUGC 155/3/3/46

HU, Hunter antigenUGC 155/3/3/47

H22, unidentified diseaseUGC 155/3/3/48

H33, unidentified diseaseUGC 155/3/3/49

ICB, Bullous ichthyosiform erythrodermaUGC 155/3/3/50

II, unidentified diseaseUGC 155/3/3/51

INH, unidentified diseaseUGC 155/3/3/52

KA, Kartagener's SyndromeUGC 155/3/3/53

KN, KoilonychiaUGC 155/3/3/54

LA, Leucocyte antigensUGC 155/3/3/55

LE, Ectopia lentisUGC 155/3/3/56

LI, Lipoma draft pedigree chartUGC 155/3/3/57

LS, Laustia pedigreesUGC 155/3/3/58

MA, Marfan's SyndromeUGC 155/3/3/59

MD, Muscular dystrophyUGC 155/3/3/60

MI, Milroy's DiseaseUGC 155/3/3/61

MT, Mt a antigenUGC 155/3/3/62

MX, MonilethrixUGC 155/3/3/63

NE, NeurofibromatosisUGC 155/3/3/64

Correspondence between Renwick, Dr Atef K Sayed, and Dr Robin M BannermanUGC 155/3/3/65

Papers on acoustic neuromaniaUGC 155/3/3/66

NP, Nail-Patella Syndrome (Hereditary osteo-onycho-dystrophy/dysplasia)UGC 155/3/3/67

NV, Nevoid basal cell carcinomaUGC 155/3/3/68

NY, NystagmusUGC 155/3/3/69

OA, Optic atrophyUGC 155/3/3/70

OI, Osteogenesis imperfectaUGC 155/3/3/71

OP, Oculo-pharyngeal myopathyUGC 155/3/3/72

OT, OtosclerosisUGC 155/3/3/73

PA, PachyonychiaUGC 155/3/3/74

PD, PolydactylyUGC 155/3/3/75

PE, Pelger-Huet AnomalyUGC 155/3/3/76

PK(U), PhenylketonuriaUGC 155/3/3/77

PO1, Familial polyposis coliUGC 155/3/3/78

PO2, Gardner's SyndromeUGC 155/3/3/79

PR, Pre-auricular sinusUGC 155/3/3/80

PV, Acro-Pectoro-Vertebral DysplasiaUGC 155/3/3/81

PX, Xeroderma pigmentosumUGC 155/3/3/82

PXE, Pseudoxanthoma elasticumUGC 155/3/3/83

RA, Red cell antigenUGC 155/3/3/84

RDD, Honeycomb retinal degeneration of DoyneUGC 155/3/3/85

RDM, Pseudo-inflammatory macular dystrophyUGC 155/3/3/86

RN, Radicular neuropathyUGC 155/3/3/87

RP, retinitus pigmentosaUGC 155/3/3/88

SC, Spastic paraplegiaUGC 155/3/3/89

SF, Symphalangism (Stiff Fingers)UGC 155/3/3/90

SH, Short palateUGC 155/3/3/91

SP, Small Patella SyndromeUGC 155/3/3/92

SW, Swann antigenUGC 155/3/3/93

SY, Syndactyly with hypertelorism (Mohr's Syndrome)UGC 155/3/3/94

SZ, unidentified diseaseUGC 155/3/3/95

SSE, Self-healing Squamous EpitheliomaUGC 155/3/3/96

TB, Thyroxine bindingUGC 155/3/3/97

TE, TelangiectasiaUGC 155/3/3/98

TF, Transferrin locusUGC 155/3/3/99

Torkildsen antigenUGC 155/3/3/100

TP, Triosephosphate isomerase deficiencyUGC 155/3/3/101

TS, Tuberous sclerosisUGC 155/3/3/102

TY, TylosisUGC 155/3/3/103

WA, Waardenburg's SyndromeUGC 155/3/3/104

WE, antigen VelUGC 155/3/3/105

WM, White Mouth (White sponge naevus)UGC 155/3/3/106

X chromosome-linked main conditionUGC 155/3/3/107

Y pedigree chartsUGC 155/3/3/108

Z pedigree chartsUGC 155/3/3/109

Pedigrees: chromosomal abnormalityUGC 155/3/4

Pedigrees: non-diseaseUGC 155/3/5

Logarithm of Odds (LOD)UGC 155/3/6

Linkage materialUGC 155/3/7

Maps and clustersUGC 155/3/8

Work of others geneticistsUGC 155/3/9

Miscellaneous genetics researchUGC 155/3/10

Material relating to Renwick's later research interestsUGC 155/3/11

Renwick material relating to the funding of researchUGC 155/3/12

PublicationsUGC 155/4

Lectures and conferencesUGC 155/5

Societies and organisationsUGC 155/6

Correspondence filesUGC 155/7