Results 41 to 50 of about 138 (79)
The RCK1 domain of the human BKCa channel transduces Ca2+ binding into structural rearrangements. [PDF]
J Gen Physiol, 2010 Yusifov T +4 more
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Detection of aneuploidies by paralogous sequence quantification. [PDF]
J Med Genet, 2004 Deutsch S +5 more
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Primary hip and knee replacement surgery: Ontario criteria for case selection and surgical priority. [PDF]
Qual Health Care, 1996 Naylor CD, Williams JI.
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Alport syndrome and mental retardation: clinical and genetic dissection of the contiguous gene deletion syndrome in Xq22.3 (ATS-MR). [PDF]
J Med Genet, 2002 Meloni I +10 more
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The prevalence of MADH4 and BMPR1A mutations in juvenile polyposis and absence of BMPR2, BMPR1B, and ACVR1 mutations. [PDF]
J Med Genet, 2004 Howe JR +12 more
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Multiple roles of the Y chromosome in the biology of Drosophila melanogaster. [PDF]
ScientificWorldJournal, 2010 Piergentili R.
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Tragic history of the VII International Congress of Genetics. [PDF]
Genetics, 2003 Soyfer VN.
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