Results
|
21.
|
|
|
22.
|
|
|
23.
|
|
|
24.
|
|
|
25.
|
Four USH2A founder mutations underlie the majority of Usher syndrome type 2 cases among non-Ashkenazi Jews. [electronic resource] by
- Auslender, Noa
- Bandah, Dikla
- Rizel, Leah
- Behar, Doron M
- Shohat, Mordechai
- Banin, Eyal
- Allon-Shalev, Stavit
- Sharony, Reuven
- Sharon, Dror
- Ben-Yosef, Tamar
Producer: 20080811
In:
Genetic testing vol. 12
Availability: No items available.
|
|
26.
|
Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene. [electronic resource] by
- Tzur, Shay
- Rosset, Saharon
- Shemer, Revital
- Yudkovsky, Guennady
- Selig, Sara
- Tarekegn, Ayele
- Bekele, Endashaw
- Bradman, Neil
- Wasser, Walter G
- Behar, Doron M
- Skorecki, Karl
Producer: 20100907
In:
Human genetics vol. 128
Availability: No items available.
|
|
27.
|
Erratum to: Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5. [electronic resource] by
- Magen, Daniella
- Ofir, Ayala
- Berger, Liron
- Goldsher, Dorit
- Eran, Ayelet
- Katib, Nasser
- Nijem, Yousif
- Vlodavsky, Euvgeni
- Tzur, Shay
- Behar, Doron M
- Fellig, Yakov
- Mandel, Hanna
Producer: 20150413
In:
Human genetics vol. 134
Availability: No items available.
|
|
28.
|
Contrasting patterns of Y chromosome variation in Ashkenazi Jewish and host non-Jewish European populations. [electronic resource] by
- Behar, Doron M
- Garrigan, Daniel
- Kaplan, Matthew E
- Mobasher, Zahra
- Rosengarten, Dror
- Karafet, Tatiana M
- Quintana-Murci, Lluis
- Ostrer, Harry
- Skorecki, Karl
- Hammer, Michael F
Producer: 20040427
In:
Human genetics vol. 114
Availability: No items available.
|
|
29.
|
The Genographic Project public participation mitochondrial DNA database. [electronic resource] by
- Behar, Doron M
- Rosset, Saharon
- Blue-Smith, Jason
- Balanovsky, Oleg
- Tzur, Shay
- Comas, David
- Mitchell, R John
- Quintana-Murci, Lluis
- Tyler-Smith, Chris
- Wells, R Spencer
Producer: 20071127
In:
PLoS genetics vol. 3
Availability: No items available.
|
|
30.
|
Insights into the demographic history of African Pygmies from complete mitochondrial genomes. [electronic resource] by
- Batini, Chiara
- Lopes, Joao
- Behar, Doron M
- Calafell, Francesc
- Jorde, Lynn B
- van der Veen, Lolke
- Quintana-Murci, Lluis
- Spedini, Gabriella
- Destro-Bisol, Giovanni
- Comas, David
Producer: 20110224
In:
Molecular biology and evolution vol. 28
Availability: No items available.
|
|
31.
|
The Basque paradigm: genetic evidence of a maternal continuity in the Franco-Cantabrian region since pre-Neolithic times. [electronic resource] by
- Behar, Doron M
- Harmant, Christine
- Manry, Jeremy
- van Oven, Mannis
- Haak, Wolfgang
- Martinez-Cruz, Begoña
- Salaberria, Jasone
- Oyharçabal, Bernard
- Bauduer, Frédéric
- Comas, David
- Quintana-Murci, Lluis
Producer: 20120713
In:
American journal of human genetics vol. 90
Availability: No items available.
|
|
32.
|
A novel 154-bp deletion in the human mitochondrial DNA control region in healthy individuals. [electronic resource] by
- Behar, Doron M
- Blue-Smith, Jason
- Soria-Hernanz, David F
- Tzur, Shay
- Hadid, Yarin
- Bormans, Concetta
- Moen, Alexander
- Tyler-Smith, Chris
- Quintana-Murci, Lluis
- Wells, R Spencer
Producer: 20090108
In:
Human mutation vol. 29
Availability: No items available.
|
|
33.
|
African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans. [electronic resource] by
- Behar, Doron M
- Rosset, Saharon
- Tzur, Shay
- Selig, Sara
- Yudkovsky, Guennady
- Bercovici, Sivan
- Kopp, Jeffrey B
- Winkler, Cheryl A
- Nelson, George W
- Wasser, Walter G
- Skorecki, Karl
Producer: 20100825
In:
Human molecular genetics vol. 19
Availability: No items available.
|
|
34.
|
Complex cytogenetic rearrangements at the DURS1 locus in syndromic Duane retraction syndrome. [electronic resource] by
- Baris, Hagit N
- Chan, Wai-Man
- Andrews, Caroline
- Behar, Doron M
- Donovan, Diana J
- Morton, Cynthia C
- Ranells, Judith
- Pal, Tuya
- Ligon, Azra H
- Engle, Elizabeth C
Publication details: Clinical case reports 10 2013
In:
Clinical case reports vol. 1
Availability: No items available.
|
|
35.
|
Population expansion in the North African late Pleistocene signalled by mitochondrial DNA haplogroup U6. [electronic resource] by
- Pereira, Luísa
- Silva, Nuno M
- Franco-Duarte, Ricardo
- Fernandes, Verónica
- Pereira, Joana B
- Costa, Marta D
- Martins, Haidé
- Soares, Pedro
- Behar, Doron M
- Richards, Martin B
- Macaulay, Vincent
Producer: 20110218
In:
BMC evolutionary biology vol. 10
Availability: No items available.
|
|
36.
|
Identification of a novel mutation in the PNLIP gene in two brothers with congenital pancreatic lipase deficiency. [electronic resource] by
- Behar, Doron M
- Basel-Vanagaite, Lina
- Glaser, Fabian
- Kaplan, Marielle
- Tzur, Shay
- Magal, Nurit
- Eidlitz-Markus, Tal
- Haimi-Cohen, Yishay
- Sarig, Galit
- Bormans, Concetta
- Shohat, Mordechai
- Zeharia, Avraham
Producer: 20140928
In:
Journal of lipid research vol. 55
Availability: No items available.
|
|
37.
|
Multiple origins of Ashkenazi Levites: Y chromosome evidence for both Near Eastern and European ancestries. [electronic resource] by
- Behar, Doron M
- Thomas, Mark G
- Skorecki, Karl
- Hammer, Michael F
- Bulygina, Ekaterina
- Rosengarten, Dror
- Jones, Abigail L
- Held, Karen
- Moses, Vivian
- Goldstein, David
- Bradman, Neil
- Weale, Michael E
Producer: 20031121
In:
American journal of human genetics vol. 73
Availability: No items available.
|
|
38.
|
High-resolution mtDNA evidence for the late-glacial resettlement of Europe from an Iberian refugium. [electronic resource] by
- Pereira, Luísa
- Richards, Martin
- Goios, Ana
- Alonso, Antonio
- Albarrán, Cristina
- Garcia, Oscar
- Behar, Doron M
- Gölge, Mukaddes
- Hatina, Jiri
- Al-Gazali, Lihadh
- Bradley, Daniel G
- Macaulay, Vincent
- Amorim, António
Producer: 20050414
In:
Genome research vol. 15
Availability: No items available.
|
|
39.
|
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5. [electronic resource] by
- Magen, Daniella
- Ofir, Ayala
- Berger, Liron
- Goldsher, Dorit
- Eran, Ayelet
- Katib, Nasser
- Katib, Nassser
- Nijem, Yousif
- Vlodavsky, Euvgeni
- Tzur, Shay
- Zur, Shay
- Behar, Doron M
- Fellig, Yakov
- Mandel, Hanna
Producer: 20150413
In:
Human genetics vol. 134
Availability: No items available.
|
|
40.
|
MtDNA evidence for a genetic bottleneck in the early history of the Ashkenazi Jewish population. [electronic resource] by
- Behar, Doron M
- Hammer, Michael F
- Garrigan, Daniel
- Villems, Richard
- Bonne-Tamir, Batsheva
- Richards, Martin
- Gurwitz, David
- Rosengarten, Dror
- Kaplan, Matthew
- Della Pergola, Sergio
- Quintana-Murci, Lluis
- Skorecki, Karl
Producer: 20041102
In:
European journal of human genetics : EJHG vol. 12
Availability: No items available.
|