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A genomic screen of autism: evidence for a multilocus etiology.
Risch N, Spiker D, Lotspeich L, Nouri N, Hinds D, Hallmayer J, Kalaydjieva L, McCague P, Dimiceli S, Pitts T, Nguyen L, Yang J, Harper C, Thorpe D, Vermeer S, Young H, Hebert J, Lin A, Ferguson J, Chiotti C, Wiese-Slater S, Rogers T, Salmon B, Nicholas P, Petersen PB, Pingree C, McMahon W, Wong DL, Cavalli-Sforza LL, Kraemer HC, Myers RM. Risch N, et al. Among authors: hebert j. Am J Hum Genet. 1999 Aug;65(2):493-507. doi: 10.1086/302497. Am J Hum Genet. 1999. PMID: 10417292 Free PMC article.
Demographic history of India and mtDNA-sequence diversity.
Mountain JL, Hebert JM, Bhattacharyya S, Underhill PA, Ottolenghi C, Gadgil M, Cavalli-Sforza LL. Mountain JL, et al. Among authors: hebert jm. Am J Hum Genet. 1995 Apr;56(4):979-92. Am J Hum Genet. 1995. PMID: 7717409 Free PMC article.
Autism and the X chromosome. Multipoint sib-pair analysis.
Hallmayer J, Hebert JM, Spiker D, Lotspeich L, McMahon WM, Petersen PB, Nicholas P, Pingree C, Lin AA, Cavalli-Sforza LL, Risch N, Ciaranello RD. Hallmayer J, et al. Among authors: hebert jm. Arch Gen Psychiatry. 1996 Nov;53(11):985-9. doi: 10.1001/archpsyc.1996.01830110021003. Arch Gen Psychiatry. 1996. PMID: 8911221
Geographic clustering of human Y-chromosome haplotypes.
Ruiz Linares A, Nayar K, Goldstein DB, Hebert JM, Seielstad MT, Underhill PA, Lin AA, Feldman MW, Cavalli Sforza LL. Ruiz Linares A, et al. Among authors: hebert jm. Ann Hum Genet. 1996 Sep;60(5):401-8. doi: 10.1111/j.1469-1809.1996.tb00438.x. Ann Hum Genet. 1996. PMID: 8912793
Wilson's disease in Israel: a genetic and epidemiological study.
Bonné-Tamir B, Frydman M, Agger MS, Bekeer R, Bowcock AM, Hebert JM, Cavalli-Sforza LL, Farrer LA. Bonné-Tamir B, et al. Among authors: hebert jm. Ann Hum Genet. 1990 May;54(2):155-68. doi: 10.1111/j.1469-1809.1990.tb00372.x. Ann Hum Genet. 1990. PMID: 2382969
1,819 results