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Items: 11

1.

Characterization of 12 silent alleles of the human butyrylcholinesterase (BCHE) gene.

Primo-Parmo SL, Bartels CF, Wiersema B, van der Spek AF, Innis JW, La Du BN.

Am J Hum Genet. 1996 Jan;58(1):52-64.

2.
3.

A family segregating for E1j and E1k at cholinesterase locus 1.

Evans RT, Iqbal J, Dietz AA, Lubrano T, Rubinstein HM.

J Med Genet. 1980 Dec;17(6):464-7.

4.

Cause of the heterogeneity of 'silent' plasma cholinesterase variants.

Das PK.

Biochem J. 1971 Oct;124(5):45P-46P. No abstract available.

5.

Improved method for the differentiation of cholinesterase variants.

Dietz AA, Rubinstein HM, Lubrano T, Hodges LK.

Am J Hum Genet. 1972 Jan;24(1):58-64. No abstract available.

6.

Properties of the C5 variant form of human serum cholinesterase.

Scott EM, Rowers RF.

Am J Hum Genet. 1974 Mar;26(2):189-94. No abstract available.

7.

Identification of a frameshift mutation responsible for the silent phenotype of human serum cholinesterase, Gly 117 (GGT----GGAG).

Nogueira CP, McGuire MC, Graeser C, Bartels CF, Arpagaus M, Van der Spek AF, Lightstone H, Lockridge O, La Du BN.

Am J Hum Genet. 1990 May;46(5):934-42.

8.

New allele at cholinesterase locus 1.

Garry PJ, Dietz AA, Lubrano T, Ford PC, James K, Rubinstein HM.

J Med Genet. 1976 Feb;13(1):38-42.

9.

A third type of serum cholinesterase deficiency in Eskimos.

Scott EM, Wright RC.

Am J Hum Genet. 1976 May;28(3):253-6.

10.

E1j, a quantitative variant at cholinesterase locus 1: immunological evidence.

Rubinstein HM, Dietz AA, Lubrano T, Garry PJ.

J Med Genet. 1976 Feb;13(1):43-5.

11.

E1k, another quantitative variant at cholinesterase locus 1.

Rubinstein HM, Dietz AA, Lubrano T.

J Med Genet. 1978 Feb;15(1):27-9.

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