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:"Morash, B A"'
Refine your search
Availability
Limit to records with available items
Authors
Guernsey, D L
Lee, C L
Morash, B A
Nassar, B A
Riddell, D C
Rowden, G
Tan, M H
Too, C K
Ur, E
Wilkinson, M
Show more
Show less
Topics
Adult
Aged
Aging
Animals
Animals, Newborn
Carcinoma, Renal Cell
Cell Division
Chromosome Aberrations
Codon
DNA
Exons
Female
Gene Expression
Heterozygote
Humans
Hyperlipoproteinemia Type II
Immunohistochemistry
Male
genetics
metabolism
Show more
Show less
Languages
English
Your search returned 3 results.
Sort
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
1.
Pituitary leptin gene expression is reduced by neonatal androgenization of female rats.
[electronic resource]
by
Morash, B A
Ur, E
Wilkinson, M
Producer:
20020705
In:
Pituitary
vol. 4
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
2.
Establishment and characterization of a renal cell carcinoma line from a patient with von Hippel-Lindau syndrome.
[electronic resource]
by
Morash, B A
Lee, C L
Rowden, G
Riddell, D C
Guernsey, D L
Producer:
19970717
In:
Cancer genetics and cytogenetics
vol. 96
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
3.
A novel mutation in Exon 4 of the low density lipoprotein receptor gene resulting in heterozygous familial hypercholesterolemia associated with decreased ligand binding.
[electronic resource]
by
Morash, B A
Tan, M H
Nassar, B A
Too, C K
Guernsey, D L
Producer:
19980526
In:
Atherosclerosis
vol. 136
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)