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Items: 10

1.

A "new" blood group character related to the ABO system.

BHENDE YM, DESHPANDE CK, BHATIA HM, SANGER R, RACE RR, MORGAN WT, WATKINS WM.

Lancet. 1952 May 3;1(6714):903-4. No abstract available.

PMID:
14918471
2.
3.

A new h allele detected in Europe has a missense mutationin alpha(1,2)-fucosyltransferase motif II.

Wagner T, Vadon M, Staudacher E, Schmarda A, Gassner C, Helmberg W, Lanzer G, Flegel WA, Wagner FF.

Transfusion. 2001 Jan;41(1):31-8.

PMID:
11161242
4.

Point mutations and deletion responsible for the Bombay H null and the Reunion H weak blood groups.

Fernandez-Mateos P, Cailleau A, Henry S, Costache M, Elmgren A, Svensson L, Larson G, Samuelsson BE, Oriol R, Mollicone R.

Vox Sang. 1998;75(1):37-46.

PMID:
9745152
5.

Missense mutation of FUT1 and deletion of FUT2 are responsible for Indian Bombay phenotype of ABO blood group system.

Koda Y, Soejima M, Johnson PH, Smart E, Kimura H.

Biochem Biophys Res Commun. 1997 Sep 8;238(1):21-5.

PMID:
9299444
6.

Wide variety of point mutations in the H gene of Bombay and para-Bombay individuals that inactivate H enzyme.

Kaneko M, Nishihara S, Shinya N, Kudo T, Iwasaki H, Seno T, Okubo Y, Narimatsu H.

Blood. 1997 Jul 15;90(2):839-49.

7.

Polymorphism of the h allele and the population frequency of sporadic nonfunctional alleles.

Wagner FF, Flegel WA.

Transfusion. 1997 Mar;37(3):284-90. Erratum in: Transfusion 1997 Jun;37(6):674.

PMID:
9122901
8.

Heterogeneity of the human H blood group alpha(1,2)fucosyltransferase gene among para-Bombay individuals.

Yu LC, Yang YH, Broadberry RE, Chen YH, Lin M.

Vox Sang. 1997;72(1):36-40.

PMID:
9031499
9.

Molecular basis for H blood group deficiency in Bombay (Oh) and para-Bombay individuals.

Kelly RJ, Ernst LK, Larsen RD, Bryant JG, Robinson JS, Lowe JB.

Proc Natl Acad Sci U S A. 1994 Jun 21;91(13):5843-7.

10.

H-deficient blood groups ( Bombay) of Reunion Island.

Gerard G, Vitrac D, Le Pendu J, Muller A, Oriol R.

Am J Hum Genet. 1982 Nov;34(6):937-47.

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