Difficulty in LW typing as revealed by a family study.

Abstract:

:A family is described in which two members of the second generation are of the phenotype LW3. In the course of the investigation the mother of the LW3 propositus was at first believed to be phenotypically LW3 as well. Eventually, it was shown that she is, in fact, phenotypically LW2 but that her R-1 (no D), LWlw, genotype had resulted in less LW being present on her red blood cells than is expected in LW2 persons. This reduced level of LW could not be detected with one example of anti-LW made by an LW3 individual.

journal_name

Transfusion

journal_title

Transfusion

authors

Behzad O,Pothiawala M,Rolih SD,Issitt PD,Lee CL

doi

10.1046/j.1537-2995.1978.18478251248.x

subject

Has Abstract

pub_date

1978-07-01 00:00:00

pages

488-92

issue

4

eissn

0041-1132

issn

1537-2995

journal_volume

18

pub_type

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