scholarly journals The Founder Mutation MSH2*1906G→C Is an Important Cause of Hereditary Nonpolyposis Colorectal Cancer in the Ashkenazi Jewish Population

2002 ◽  
Vol 71 (6) ◽  
pp. 1395-1412 ◽  
Author(s):  
W.D. Foulkes ◽  
I. Thiffault ◽  
S.B. Gruber ◽  
M. Horwitz ◽  
N. Hamel ◽  
...  
Keyword(s):  
Colorectal Cancer ◽  
Jewish Population ◽  
Hereditary Nonpolyposis Colorectal Cancer ◽  
Founder Mutation ◽  
Ashkenazi Jewish ◽  
Ashkenazi Jewish Population ◽  
Hereditary Nonpolyposis

A founder mutation inCOL4A3causes autosomal recessive Alport syndrome in the Ashkenazi Jewish population

2013 ◽  
Vol 86 (2) ◽  
pp. 155-160 ◽  
Author(s):  
B.D. Webb ◽  
T. Brandt ◽  
L. Liu ◽  
C. Jalas ◽  
J. Liao ◽  
...  
Keyword(s):  
Jewish Population ◽  
Alport Syndrome ◽  
Autosomal Recessive ◽  
Founder Mutation ◽  
Ashkenazi Jewish ◽  
Ashkenazi Jewish Population

A founder mutation in the MPL gene causes congenital amegakaryocytic thrombocytopenia (CAMT) in the Ashkenazi Jewish population

2011 ◽  
Vol 47 (1) ◽  
pp. 79-83 ◽  
Author(s):  
Chaim Jalas ◽  
Sylvia L. Anderson ◽  
Tova Laufer ◽  
Kristina Martimucci ◽  
Alex Bulanov ◽  
...  
Keyword(s):  
Jewish Population ◽  
Founder Mutation ◽  
Ashkenazi Jewish ◽  
Ashkenazi Jewish Population

A founder mutation in theTCIRG1gene causes osteopetrosis in the Ashkenazi Jewish population

2014 ◽  
Vol 88 (1) ◽  
pp. 74-79 ◽  
Author(s):  
S.L. Anderson ◽  
C. Jalas ◽  
A. Fedick ◽  
K.F. Reid ◽  
T.O. Carpenter ◽  
...  
Keyword(s):  
Jewish Population ◽  
Founder Mutation ◽  
Ashkenazi Jewish ◽  
Ashkenazi Jewish Population
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