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Detection of the S252W mutation in fibroblast growth factor receptor 2 (FGFR2) in fetal DNA from maternal plasma in a pregnancy affected by Apert syndrome.
Prenat Diagn. 2011 Feb; 31(2):218-20.PD

Authors

No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Letter

Language

eng

PubMed ID

21268044

Citation

Au, Patrick K C., et al. "Detection of the S252W Mutation in Fibroblast Growth Factor Receptor 2 (FGFR2) in Fetal DNA From Maternal Plasma in a Pregnancy Affected By Apert Syndrome." Prenatal Diagnosis, vol. 31, no. 2, 2011, pp. 218-20.
Au PK, Kwok YK, Leung KY, et al. Detection of the S252W mutation in fibroblast growth factor receptor 2 (FGFR2) in fetal DNA from maternal plasma in a pregnancy affected by Apert syndrome. Prenat Diagn. 2011;31(2):218-20.
Au, P. K., Kwok, Y. K., Leung, K. Y., Tang, L. Y., Tang, M. H., & Lau, E. T. (2011). Detection of the S252W mutation in fibroblast growth factor receptor 2 (FGFR2) in fetal DNA from maternal plasma in a pregnancy affected by Apert syndrome. Prenatal Diagnosis, 31(2), 218-20. https://doi.org/10.1002/pd.2672
Au PK, et al. Detection of the S252W Mutation in Fibroblast Growth Factor Receptor 2 (FGFR2) in Fetal DNA From Maternal Plasma in a Pregnancy Affected By Apert Syndrome. Prenat Diagn. 2011;31(2):218-20. PubMed PMID: 21268044.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Detection of the S252W mutation in fibroblast growth factor receptor 2 (FGFR2) in fetal DNA from maternal plasma in a pregnancy affected by Apert syndrome. AU - Au,Patrick K C, AU - Kwok,Yvonne K Y, AU - Leung,K Y, AU - Tang,Linda Y F, AU - Tang,Mary H Y, AU - Lau,Elizabeth T, Y1 - 2011/01/04/ PY - 2010/07/22/received PY - 2010/10/06/revised PY - 2010/11/06/accepted PY - 2011/1/27/entrez PY - 2011/1/27/pubmed PY - 2011/4/16/medline SP - 218 EP - 20 JF - Prenatal diagnosis JO - Prenat Diagn VL - 31 IS - 2 SN - 1097-0223 UR - https://www.unboundmedicine.com/medline/citation/21268044/Detection_of_the_S252W_mutation_in_fibroblast_growth_factor_receptor_2__FGFR2__in_fetal_DNA_from_maternal_plasma_in_a_pregnancy_affected_by_Apert_syndrome_ L2 - https://doi.org/10.1002/pd.2672 DB - PRIME DP - Unbound Medicine ER -