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:"HANHART, E"', page 3 of 3
Refine your search
Availability
Limit to records with available items
Authors
Allen, G
Benda, C E
Böök, J A
Carter, C O
Chu, E H
DOLIVO, G
Denninghof, K
FANCONI, G
Ford, C E
HANHART, E
Hanhart, E
Hanhart, E J
Iqbal, M
Irdani, T
JEQUIER, M
Jervis, G
Johnson, H
Johnson, W D
Kälin, A
Zellweger, H
Show more
Show less
Topics
Adolescent
Adult
Aged
Animals
Child
Diabetes Mellitus
Female
Genetics, Medical
Heredity
Humans
Hypersensitivity
Immune System Diseases
Infant, Newborn
Intellectual Disability
Male
Middle Aged
Pedigree
Switzerland
etiology
genetics
Show more
Show less
Languages
English
French
German
Italian
Undetermined
Your search returned 47 results.
Sort
First
Previous
1
2
3
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
41.
[Dominant heredity of progressive muscular dystrophy in family in Vaud].
[electronic resource]
by
JEQUIER, M
HANHART, E
Producer:
20030501
In:
Acta neurologica et psychiatrica Belgica
vol. 54
Availability:
No items available.
Save to lists
Add to cart
(remove)
42.
[Significance of hereditary homo- and heterogeny in hereditary prognosis of clinical signs, especially diabetes mellitus and recessive deafmutism].
[electronic resource]
by
HANHART, E
LUCHSINGER, R
Producer:
20040215
In:
Schweizerische medizinische Wochenschrift
vol. 81
Availability:
No items available.
Save to lists
Add to cart
(remove)
43.
A new genetic variant of the spinal muscular atrophies in infancy.
[electronic resource]
by
Zellweger, H
Hanhart, E
Schneider, H J
Producer:
19730308
In:
Journal of medical genetics
vol. 9
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
44.
Characterization and sequence analysis of a Streptomyces rochei A2 endoglucanase-encoding gene.
[electronic resource]
by
Perito, B
Hanhart, E
Irdani, T
Iqbal, M
McCarthy, A J
Mastromei, G
Producer:
19941118
In:
Gene
vol. 148
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
45.
[Familial, juvenile nephronophthisis (idiopathic parenchymal contracted kidney)].
[electronic resource]
by
FANCONI, G
HANHART, E
von ALBERTINI, A
UHLINGER, E
DOLIVO, G
PRADER, A
Producer:
20040215
In:
Helvetica paediatrica acta
vol. 6
Availability:
No items available.
Save to lists
Add to cart
(remove)
46.
Tympanic membrane thermometry in the care of out-of-hospital patients.
[electronic resource]
by
Weiss, S J
Hanhart, E J
McBride, R
Johnson, H
Denninghof, K
Johnson, W D
Producer:
19950125
In:
Annals of emergency medicine
vol. 25
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
47.
Mongolism.
[electronic resource]
by
Allen, G
Benda, C E
Böök, J A
Carter, C O
Ford, C E
Chu, E H
Hanhart, E
Jervis, G
Langdon-Down, W
Lejeune, J
Nishimura, H
Oster, J
Penrose, L S
Polani, P E
Potter, E L
Stern, C
Turpin, R
Warkany, J
Yannet, H
Producer:
20071024
In:
American journal of human genetics
vol. 13
Availability:
No items available.
Save to lists
Add to cart
(remove)
First
Previous
1
2
3