A novel polymorphism associated with lactose tolerance in Africa: multiple causes for lactase persistence? (English)
- New search for: Ingram, Catherine J. E.
- New search for: Elamin, Mohamed F.
- New search for: Mulcare, Charlotte A.
- New search for: Weale, Michael E.
- New search for: Tarekegn, Ayele
- New search for: Raga, Tamiru Oljira
- New search for: Bekele, Endashaw
- New search for: Elamin, Farouk M.
- New search for: Thomas, Mark G.
- New search for: Bradman, Neil
- New search for: Swallow, Dallas M.
- New search for: Ingram, Catherine J. E.
- New search for: Elamin, Mohamed F.
- New search for: Mulcare, Charlotte A.
- New search for: Weale, Michael E.
- New search for: Tarekegn, Ayele
- New search for: Raga, Tamiru Oljira
- New search for: Bekele, Endashaw
- New search for: Elamin, Farouk M.
- New search for: Thomas, Mark G.
- New search for: Bradman, Neil
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In:
Human Genetics
;
120
, 6
; 779-788
;
2006
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ISSN:
- Article (Journal) / Electronic Resource
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Title:A novel polymorphism associated with lactose tolerance in Africa: multiple causes for lactase persistence?
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Contributors:Ingram, Catherine J. E. ( author ) / Elamin, Mohamed F. ( author ) / Mulcare, Charlotte A. ( author ) / Weale, Michael E. ( author ) / Tarekegn, Ayele ( author ) / Raga, Tamiru Oljira ( author ) / Bekele, Endashaw ( author ) / Elamin, Farouk M. ( author ) / Thomas, Mark G. ( author ) / Bradman, Neil ( author )
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Published in:Human Genetics ; 120, 6 ; 779-788
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Publisher:
- New search for: Springer-Verlag
- New search for: Springer
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Place of publication:Berlin
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Publication date:2006
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ISSN:
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ZDBID:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
- New search for: 44.48
- Further information on Basic classification
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Keywords:
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Classification:
BKL: 44.48 Medizinische Genetik -
Source:
Table of contents – Volume 120, Issue 6
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 749
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My last visit with Friedrich Vogel: a personal remembranceRappold, Gudrun et al. | 2006
- 751
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Friedrich Vogel 1925–2006Propping, Peter / Bartram, Claus R. et al. | 2006
- 755
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Obituary: Prof. Dr. med. Dr. h. c. Friedrich Vogel (1925–2006)Sperling, Karl et al. | 2006
- 759
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Structural divergence between the human and chimpanzee genomesKehrer-Sawatzki, Hildegard / Cooper, David N. et al. | 2006
- 779
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A novel polymorphism associated with lactose tolerance in Africa: multiple causes for lactase persistence?Ingram, Catherine J. E. / Elamin, Mohamed F. / Mulcare, Charlotte A. / Weale, Michael E. / Tarekegn, Ayele / Raga, Tamiru Oljira / Bekele, Endashaw / Elamin, Farouk M. / Thomas, Mark G. / Bradman, Neil et al. | 2006
- 789
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Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2–q13.3Khan, Shahid Y. / Riazuddin, Saima / Tariq, Muhammad / Anwar, Saima / Shabbir, Muhammad I. / Riazuddin, S. Amer / Khan, Shaheen N. / Husnain, Tayyab / Ahmed, Zubair M. / Friedman, Thomas B. et al. | 2006
- 795
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Cytogenetically balanced translocations are associated with focal copy number alterationsWatson, Spencer K. / deLeeuw, Ronald J. / Horsman, Doug E. / Squire, Jeremy A. / Lam, Wan L. et al. | 2006
- 807
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Admixture in Mexico City: implications for admixture mapping of Type 2 diabetes genetic risk factorsMartinez-Marignac, Veronica L. / Valladares, Adan / Cameron, Emily / Chan, Andrea / Perera, Arjuna / Globus-Goldberg, Rachel / Wacher, Niels / Kumate, Jesús / McKeigue, Paul / O’Donnell, David et al. | 2006
- 821
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The possible role of 10398A and 16189C mtDNA variants in providing susceptibility toT2DM in two North Indian populations: a replicative studyBhat, Audesh / Koul, Anil / Sharma, Swarkar / Rai, Ekta / Bukhari, S. I. A. / Dhar, M. K. / Bamezai, R. N. K. et al. | 2006
- 827
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Mitochondrial haplogroup N9b is protective against myocardial infarction in Japanese malesNishigaki, Yutaka / Yamada, Yoshiji / Fuku, Noriyuki / Matsuo, Hitoshi / Segawa, Tomonori / Watanabe, Sachiro / Kato, Kimihiko / Yokoi, Kiyoshi / Yamaguchi, Sachiyo / Nozawa, Yoshinori et al. | 2006
- 837
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Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndromeWeksberg, Rosanna / Stachon, Andrea C. / Squire, Jeremy A. / Moldovan, Laura / Bayani, Jane / Meyn, Stephen / Chow, Eva / Bassett, Anne S. et al. | 2006
- 847
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Sequence variant in the laminin γ1 (LAMC1) gene associated with familial pelvic organ prolapseNikolova, Ganka / Lee, Hane / Berkovitz, Suzanne / Nelson, Stanley / Sinsheimer, Janet / Vilain, Eric / Rodríguez, Larissa V. et al. | 2006
- 857
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The LRRK2 Gly2385Arg variant is associated with Parkinson’s disease: genetic and functional evidenceTan, E. K. / Zhao, Y. / Skipper, L. / Tan, M. G. / Di Fonzo, A. / Sun, L. / Fook-Chong, S. / Tang, S. / Chua, E. / Yuen, Y. et al. | 2006
- 865
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Subsets of SNPs define rare genotype classes that predict ischemic heart diseaseFrikke-Schmidt, Ruth / Sing, Charles F. / Nordestgaard, Børge G. / Steffensen, Rolf / Tybjærg-Hansen, Anne et al. | 2006
- 879
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Identification of a regulatory SNP in the retinol binding protein 4 gene associated with type 2 diabetes in MongoliaMunkhtulga, Lkhagvasuren / Nakayama, Kazuhiro / Utsumi, Nanami / Yanagisawa, Yoshiko / Gotoh, Takaya / Omi, Toshinori / Kumada, Maki / Erdenebulgan, Batmunkh / Zolzaya, Khadbaatar / Lkhagvasuren, Tserenkhuu et al. | 2006
- 889
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Evidence for statistical epistasis between catechol-O-methyltransferase (COMT) and polymorphisms in RGS4, G72 (DAOA), GRM3, and DISC1: influence on risk of schizophreniaNicodemus, Kristin K. / Kolachana, Bhaskar S. / Vakkalanka, Radhakrishna / Straub, Richard E. / Giegling, Ina / Egan, Michael F. / Rujescu, Dan / Weinberger, Daniel R. et al. | 2006
- 907
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Novel human pathological mutations| 2006