CO, Co a antigen

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Includes two articles on the Co a antibody.

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