Ling Ma (L Ma)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 6

Top Topics

Intellectual Disability

Genome Wide Identification

Top Venues

Transfusion medicine (Oxford, England)

This page only lists publications with an associated author ORCID identifier.

Publications

Lili Shi, Ling Ma, Chenchen Feng, Qinping Yang
A novel FUT1*932A allele associated with the para-Bombay A phenotype in a Chinese individual. Transfusion 64 (8) (2024)
Lili Shi, Ling Ma, Chenchen Feng, Qinping Yang
A novel FUT1*932A allele associated with the para-Bombay A phenotype in a Chinese individual. Transfusion (2024)
Lili Shi, Ling Ma, Chenchen Feng, Qinping Yang
A novel FUT1*932A allele associated with the para-Bombay A phenotype in a Chinese individual. Transfusion (2024)
Lili Shi, Ling Ma, Chenchen Feng, Qinping Yang
A novel FUT1*932A allele associated with the para-Bombay A phenotype in a Chinese individual. Transfusion 64 (8) (2024)
Ling Ma, Enbo Wang, Taixiang Liu, Chengyin Huang, Wenyi Ding
Rare P k phenotype caused by a novel frameshift mutation in B3GALNT1. Transfusion medicine (Oxford, England) (2022)
Ling Ma, Y Liu
Novel missense mutation (c.284 T>C) in the ABO gene associated with the Ael phenotype. Transfusion medicine (Oxford, England) 29 (2) (2019)