Literature DB >> 4805484

Population studies in northern Sweden. IV. Frequency of the blood type p.

B Cedergren.   

Abstract

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Year:  1973        PMID： 4805484

Source DB:  PubMed          Journal:  Hereditas        ISSN： 0018-0661            Impact factor:   3.271


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  3 in total

1.  P-Null Phenotype Due to a Rare Frame-Shift Mutation and with Allo-Anti-PP1Pk Causing a Severe Hemolytic Transfusion Reaction: A Case Report with Clinical Management.

Authors:  Ashish N Kanani; Snehal B Senjaliya; Manisha M Rajapara; Judith Aeschlimann; Connie M Westhoff; Sanmukh R Joshi
Journal:  Transfus Med Hemother       Date:  2021-02-25       Impact factor: 3.747

2.  Blood group glycosphingolipid expression in kidney of an individual with the rare blood group A1 Le(a-b+) p phenotype: absence of blood group structures based on the globoseries.

Authors:  K Lindström; P A Jovall; S Ghardashkani; B E Samuelsson; M E Breimer
Journal:  Glycoconj J       Date:  1996-04       Impact factor: 2.916

3.  Two previously proposed P1/P2-differentiating and nine novel polymorphisms at the A4GALT (Pk) locus do not correlate with the presence of the P1 blood group antigen.

Authors:  Asa Hellberg; M Alan Chester; Martin L Olsson
Journal:  BMC Genet       Date:  2005-10-07       Impact factor: 2.797
  3 in total

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