Skip to main content
مکتبة رقمیه للعلوم الطبيه
Your cart is empty.
Cart
Lists
Your lists
Log in to create your own lists
Log in to your account
Your cookies
Search history
Search the catalog by:
Library catalog
Title
Author
Subject
ISBN
ISSN
Series
Call number
Search the catalog by keyword
Advanced search
Authority search
Tag cloud
Library
Log in to your account
Home
Advanced search
Results of search for 'au:"Crawfurd, M"', page 2 of 2
Refine your search
Availability
Limit to records with available items
Authors
Arnott, E J
Bannister, R
Barber, J C
Barnes, P M
Blackie, R A
Bronstein, A M
Brough, C
CRAWFURD, M D
Crawfurd, M
Crawfurd, M A
Crawfurd, M D
Gibbs, D A
JACOBS, A
MURPHY, B
Morgan, S H
PETERS, D K
Portch, J
Toghill, P J
Wilson, T M
Winter, R M
Show more
Show less
Topics
Abnormalities, Multiple
Adolescent
Adult
Child, Preschool
Chromosome Aberrations
Chromosome Disorders
Dermatoglyphics
Female
Genetic Counseling
Heterozygote
Humans
Infant, Newborn
Karyotyping
Male
Pedigree
Pregnancy
Prenatal Diagnosis
abnormalities
diagnosis
genetics
Show more
Show less
Languages
English
Your search returned 40 results.
Sort
First
Previous
1
2
Sort by:
Relevance
Popularity (most to least)
Popularity (least to most)
Author (A-Z)
Author (Z-A)
Call number (0-9 to A-Z)
Call number (Z-A to 9-0)
Publication/Copyright date: Newest to oldest
Publication/Copyright date: Oldest to newest
Acquisition date: Newest to oldest
Acquisition date: Oldest to newest
Title (A-Z)
Title (Z-A)
Unhighlight
Highlight
Select all
Clear all
Select titles to:
Add to cart
Add to list
New list
Place hold
Results
21.
Distal muscular dystrophy in an English family.
[electronic resource]
by
Sumner, D
Crawfurd, M D
Harriman, D G
Producer:
19710601
In:
Brain : a journal of neurology
vol. 94
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
22.
Inhibition of gill cilial activity and of Proteus vulgaris motility as tests for aspirin idiosyncrasy.
[electronic resource]
by
Delaney, J C
Crawfurd, M D
Roberts, C
Producer:
19760823
In:
Annals of allergy
vol. 36
Availability:
No items available.
Save to lists
Add to cart
(remove)
23.
Non-progressive cerebellar ataxia, aplasia of pupillary zone of iris, and mental subnormality (Gillespie's syndrome) affecting 3 members of a non-consanguineous family in 2 generations.
[electronic resource]
by
Crawfurd, M D
Harcourt, R B
Shaw, P A
Producer:
19800228
In:
Journal of medical genetics
vol. 16
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
24.
Studies on human phenylalanine Mono-oxygenase. I. Restricted expression.
[electronic resource]
by
Crawfurd, M D
Gibbs, D A
Sheppard, D M
Producer:
19820222
In:
Journal of inherited metabolic disease
vol. 4
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
25.
Anterior lenticonus and Alport's syndrome.
[electronic resource]
by
Arnott, E J
Crawfurd, M D
Toghill, P J
Producer:
19661023
In:
The British journal of ophthalmology
vol. 50
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
26.
A monopodal sireniform monster with dermatoglyphic and cytogenetic studies.
[electronic resource]
by
Crawfurd, M D
Ismail, S R
Wigglesworth, J S
Producer:
19670907
In:
Journal of medical genetics
vol. 3
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
27.
PATERSON-KELLY SYNDROME IN ADOLESCENCE: A REPORT OF FIVE CASES.
[electronic resource]
by
CRAWFURD, M D
JACOBS, A
MURPHY, B
PETERS, D K
Producer:
19961201
In:
British medical journal
vol. 1
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
28.
Interstitial deletions without phenotypic effect: prenatal diagnosis of a new family and brief review.
[electronic resource]
by
Barber, J C
Mahl, H
Portch, J
Crawfurd, M D
Producer:
19911108
In:
Prenatal diagnosis
vol. 11
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
29.
PATERSON-KELLY SYNDROME IN ADOLESCENCE.
[electronic resource]
by
CRAWFURD, M D
JACOBS, A
MURPHY, B
PETERS, D K
Producer:
19961201
In:
British medical journal
vol. 1
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
30.
The demonstration of monozygosity in twins discordant for sacral agenesis.
[electronic resource]
by
Crawfurd, M D
Cheshire, J
Wilson, T M
Woodhouse, C R
Producer:
19920731
In:
Journal of medical genetics
vol. 29
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
31.
Recognising placental steroid sulphatase deficiency.
[electronic resource]
by
Harkness, R A
Taylor, N F
Crawfurd, M A
Rose, F A
Producer:
19830826
In:
British medical journal (Clinical research ed.)
vol. 287
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
32.
A report on genetic registers. Based on the report of the Clinical Genetics Society Working Party.
[electronic resource]
by
Emery, A E
Brough, C
Crawfurd, M
Harper, P
Harris, R
Oakshott, G
Producer:
19790523
In:
Journal of medical genetics
vol. 15
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
33.
A further family with congenital renal proximal tubular dysgenesis.
[electronic resource]
by
MacMahon, P
Blackie, R A
House, M J
Risdon, R A
Crawfurd, M D
Producer:
19900727
In:
Journal of medical genetics
vol. 27
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
34.
Anderson-Fabry disease--family linkage studies using two polymorphic X-linked DNA probes.
[electronic resource]
by
Morgan, S H
Cheshire, J K
Wilson, T M
MacDermot, K
Crawfurd, M A
Producer:
19901227
In:
Pediatric nephrology (Berlin, Germany)
vol. 1
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
35.
Partial monosomy 7 with interstitial deletions in two infants with differing congenital abnormalities.
[electronic resource]
by
Crawfurd, M D
Kessel, I
Liberman, M
McKeown, J A
Mandalia, P Y
Ridler, M A
Producer:
19800523
In:
Journal of medical genetics
vol. 16
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
36.
Early prenatal diagnosis of Hurler's syndrome with termination of pregnancy and confirmatory findings on the fetus.
[electronic resource]
by
Crawfurd, M
Dean, M F
Hunt, D M
Johnson, D R
MacDonald, R R
Muir, H
Wright, E A
Wright, C R
Producer:
19730831
In:
Journal of medical genetics
vol. 10
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
37.
Congenital haemolytic anaemia resulting from glucose phosphate isomerase deficiency: genetics, clinical picture, and prenatal diagnosis.
[electronic resource]
by
Whitelaw, A G
Rogers, P A
Hopkinson, D A
Gordon, H
Emerson, P M
Darley, J H
Reid, C
Crawfurd, M A
Producer:
19791017
In:
Journal of medical genetics
vol. 16
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
38.
The neurological complications of Anderson-Fabry disease (alpha-galactosidase A deficiency)--investigation of symptomatic and presymptomatic patients.
[electronic resource]
by
Morgan, S H
Rudge, P
Smith, S J
Bronstein, A M
Kendall, B E
Holly, E
Young, E P
Crawfurd, M D
Bannister, R
Producer:
19900924
In:
The Quarterly journal of medicine
vol. 75
Availability:
No items available.
Save to lists
Add to cart
(remove)
39.
Investigation of three patients with the "ring syndrome", including familial transmission of ring 5, and estimation of reproductive risks.
[electronic resource]
by
MacDermot, K D
Jack, E
Cooke, A
Turleau, C
Lindenbaum, R H
Pearson, J
Patel, C
Barnes, P M
Portch, J
Crawfurd, M D
Producer:
19901205
In:
Human genetics
vol. 85
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
40.
First-trimester diagnosis of Lesch-Nyhan syndrome.
[electronic resource]
by
Gibbs, D A
McFadyen, I R
Crawfurd, M D
De Muinck Keizer, E E
Headhouse-Benson, C M
Wilson, T M
Farrant, P H
Producer:
19841231
In:
Lancet (London, England)
vol. 2
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
First
Previous
1
2