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Screening Extended Families for Genetic Hemoglobin Disorders in Pakistan
Author(s) -
Suhaib Ahmed,
Mohammed Saleem,
Bernadette Modell,
Mary Petrou
Publication year - 2002
Publication title -
new england journal of medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 19.889
H-Index - 1030
eISSN - 1533-4406
pISSN - 0028-4793
DOI - 10.1056/nejmsa013234
Subject(s) - genetic counseling , medicine , carrier testing , family history , consanguineous marriage , prenatal diagnosis , pregnancy , demography , pediatrics , consanguinity , family medicine , genetics , surgery , fetus , biology , sociology
We have investigated a strategy for identifying and counseling carriers of recessively inherited disorders in developing countries where consanguineous marriage is common. In such communities, gene variants are trapped within extended families, so that an affected child is a marker of a group at high genetic risk.

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