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:"Khan, Mohammad Nasim"'
Refine your search
Availability
Limit to records with available items
Authors
Ahmad, Wasim
Ansar, Muhammad
Bhatti, Attya
Chahrour, Maria H
Hassan, Muhammad Jawad
Irshad, Saba
Khan, Mohammad Nasim
Leal, Suzanne M
Lee, Kwanghyuk
McArthur, Nathan
Mir, Asif
Pham, Thanh L
Santos, Regie Lyn P
Tariq, Aamira
Wajid, Muhammad
Yan, Kai
Show more
Show less
Topics
Adolescent
Adult
Chromosome Aberrations
Chromosomes, Human, Pair 20
Connexin 26
Connexins
Consanguinity
Female
Genes, Recessive
Genetic Linkage
Genetic Markers
Genetic Variation
Hearing Loss
Humans
India
Lod Score
Male
Membrane Proteins
Pakistan
genetics
Show more
Show less
Languages
English
Your search returned 2 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.
Localization of a novel autosomal recessive nonsyndromic hearing impairment locus DFNB65 to chromosome 20q13.2-q13.32.
[electronic resource]
by
Tariq, Aamira
Santos, Regie Lyn P
Khan, Mohammad Nasim
Lee, Kwanghyuk
Hassan, Muhammad Jawad
Ahmad, Wasim
Leal, Suzanne M
Producer:
20061114
In:
Journal of molecular medicine (Berlin, Germany)
vol. 84
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
2.
Novel sequence variants in the TMC1 gene in Pakistani families with autosomal recessive hearing impairment.
[electronic resource]
by
Santos, Regie Lyn P
Wajid, Muhammad
Khan, Mohammad Nasim
McArthur, Nathan
Pham, Thanh L
Bhatti, Attya
Lee, Kwanghyuk
Irshad, Saba
Mir, Asif
Yan, Kai
Chahrour, Maria H
Ansar, Muhammad
Ahmad, Wasim
Leal, Suzanne M
Producer:
20060619
In:
Human mutation
vol. 26
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)