Language
English
German
^M
Dutch
Spanish
Title:
Homozygosity mapping identifies a novel GIPC3 mutation causing congenital nonsyndromic hearing loss in a Saudi family
Source:
Gene [0378-1119] Ramzan, Khushnooda yr:2013
Basic
Sorry, no full text available...
Please use the document delivery service (see below)
Holding information
Holdings in library search engine
ALBERT
Document delivery
Request document via
Library/Bibliothek
Users interested in this article also expressed an interest in the following:
description
1.
Galjaard, Robert-Jan H.
"0.5Mb Array as a First-Line Prenatal Cytogenetic Test in Cases without Ultrasound Abnormalities and its Implementation in Clinical Practice."
Human mutation
(2013): 1298-1303.
description
2.
Liebmann, M.
"Astrocytic Cx43 and Cx30 differentially modulate adult neurogenesis in mice."
Neuroscience Letters
545 (2013): 40-45.
description
3.
Ain, Q.
"The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3."
Human genetics
122.5 (2007): 445-50.
description
4.
Lo Giudice, M.
"The 9-bp deletion in region v of mtDNA: A risk factor of hearing loss and encephalomyopathy in Caucasian populations?"
Neurological sciences
34.7 (2013): 1223-1226.
description
5.
Rooryck, C.
"Prenatal diagnosis using array-CGH: a French experience."
European journal of medical genetics
56.7 (2013): 341-345.
description
6.
Wasielewski, B.
"Neuroglial activation and Cx43 expression are reduced upon transplantation of human umbilical cord blood cells after perinatal hypoxic-ischemic injury."
Brain research
1487 (2012): 39-53.
description
7.
Wichterle, H.
"What can pluripotent stem cells teach us about neurodegenerative diseases?"
Nature Neuroscience
13.7 (2010): 800-804.
description
8.
Sajnani-Perez, G.
"Isoform-specific binding of the tyrosine phosphatase PTPsigma to a ligand in developing muscle."
Molecular and cellular neurosciences
22.1 (2002): 37-48.
description
9.
Chen, G.
"New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p."
American journal of medical genetics
71.4: 467-471.
description
10.
Yatsenko, Sa.
"Application of chromosomal microarray in the evaluation of abnormal prenatal findings."
Clinical genetics
84.1 (2012): 47-54.
description
11.
Jain, Pawan K.
"A gene for recessive nonsyndromic sensorineural deafness (DFNB18) maps to the chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C gene."
Genomics
50.2 (1998): 290-292.
description
12.
Fujimoto, A.
"GJB6, of which mutations underlie Clouston syndrome, is a potential direct target gene of p63."
Journal of dermatological science
69.2 (2013): 159-166.
description
13.
Mikhaelian, M.
"Prenatal chromosomal microarray analysis: a survey of prenatal genetic counselors' experiences and attitudes."
Prenatal diagnosis
33.4 (2013): 1-7.
description
14.
Corsello, G.
"Congenital malformations."
Journal of Maternal - Fetal & Neonatal Medicine
25.S1 (2012): 25-29.
description
15.
Hargus, G.
"Differentiated Parkinson patient-derived induced pluripotent stem cells grow in the adult rodent brain and reduce motor asymmetry in Parkinsonian rats."
Proceedings of the National Academy of Sciences of the United States of America
107.36 (2010): 15921-15926.
description
16.
Liu, Su-Chun n.
"Human stem cells as a model of motoneuron development and diseases."
Annals of the New York Academy of Sciences
1198.1 (2010): 192-200.
description
17.
Inoue, H.
"Neurodegenerative disease-specific induced pluripotent stem cells research."
Journal of Pharmacological Sciences
112 (2010): 29-29.
description
18.
Schou, K V.
"Increased nuchal translucency with normal karyotype: a follow-up study of 100 cases supplemented with CGH and MLPA analyses."
Ultrasound in obstetrics & gynecology
34.6 (2009): 618-622.
description
19.
Naegele, Janice R.
"Recent advancements in stem cell and gene therapies for neurological disorders and intractable epilepsy."
Neuropharmacology
58.6 (2010): 855-864.
description
20.
Bell, F.
"Parkinson's Disease Patient-Derived Induced Pluripotent Stem Cells Free of Viral Reprogramming Factors."
Cell
136.5 (2009): 964-977.
View More...
View Less...
Select All
Clear All
Save Citations
Select Format
ProCite
EndNote
RefWorks
Reference Manager
Submit citation export
Advanced
Author
Other articles by this author? -- in
GeoRef
author:
Ramzan, Khushnooda
Al Owain, Mohammed
Allam, Rabab
Berhan, Amal
Abuharb, Gheid
Taibah, Khalid
Imtiaz, Faiqa
last name
initials
Other articles by this author? -- in
Online Contents Geosciences
author:
Ramzan, Khushnooda
Al Owain, Mohammed
Allam, Rabab
Berhan, Amal
Abuharb, Gheid
Taibah, Khalid
Imtiaz, Faiqa
last name
initials
Other articles by this author? -- using
Web of Science
author:
Ramzan, Khushnooda
Al Owain, Mohammed
Allam, Rabab
Berhan, Amal
Abuharb, Gheid
Taibah, Khalid
Imtiaz, Faiqa
last name
initials
Web Search
Find related information in
a Web Search Engine
Excite
Google
HotBot
Ixquick
ZOO
Ask
Yahoo!
Bing
Naver
Search Terms:
Search for related information in
Google Scholar
Article Title
Author Name
Journal Title
Other Search
Search Terms:
A service provided by the
Library of the Wissenschaftspark Albert Einstein
, Potsdam, Germany.
© 2005 SFX by Ex Libris Inc.