Predisposition to the fragile X syndrome in Jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotype (Q35239079)
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(P31) (Q13442814)
(P304) 103-112
(P407) (Q1860)
(P433) 1
(P478) 60
(P577) Wednesday, January 1, 1997
(P921) (Q221472)
(P1433) (Q4744249)
(P1476) "Predisposition to the fragile X syndrome in Jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotype" (language: en)
(P2093) T C Falik-Zaccai
E Shachak
M Yalon
Z Lis
Z Borochowitz
J N Macpherson
D L Nelson
E E Eichler
(P2860) (Q52008919)
(Q52012043)
(Q41653200)
(Q33595415)
(Q52221941)
(Q34061045)
(Q36756225)
(Q35194459)
(Q47379137)
(Q39111985)
(Q39111532)
(Q35644624)
(Q35643934)
(Q36652793)
(Q33672066)
(Q33673680)
(Q52078138)
(Q45158087)
(Q28235115)
(Q35195860)
(Q37600444)
(Q46557296)
(Q52201278)
(Q52039937)
(Q45285212)
(Q44176077)
(Q52025538)
(Q50344958)
(Q52069572)
(Q72092175)
(Q72761290)
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(Q70024577)
(Q72449243)
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(Q67482175)
(Q67482177)
(Q70497047)
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