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pregnancy combined with hemophilia gene carrier相关文献:
Four Decades of Carrier Detection and Prenatal Diagnosis in Hemophilia A: Historical Overview, State of the Art and Future Directions.
Dardik R, Janczar S, Lalezari S, Avishai E, Levy-Mendelovich S, Barg AA, Martinowitz U, Babol-Pokora K, Mlynarski W, Kenet G.
Int J Mol Sci. 2023 Jul 24;24(14):11846. doi: 10.3390/ijms241411846.
PMID:37511607
Carrier detection in the hemophilias.
Lillicrap DP, White BN, Holden JJ, Giles AR.
Am J Hematol. 1987 Nov;26(3):285-96. doi: 10.1002/ajh.2830260311.
PMID:2890293
Cost-effectiveness in establishing hemophilia carrier detection and prenatal diagnosis services in a developing country with limited health resources.
Sasanakul W, Chuansumrit A, Ajjimakorn S, Krasaesub S, Sirachainan N, Chotsupakarn S, Kadegasem P, Rurgkhum S.
Southeast Asian J Trop Med Public Health. 2003 Dec;34(4):891-8.
PMID:15115107
Detection of hemophilia carriers during pregnancy.
Hoyer LW, Carta CA, Mahoney MJ.
Blood. 1982 Dec;60(6):1407-10.
PMID:6814553
Prenatal diagnosis for hemophilia A (intron 22 inversion) reveals a rare association with Klinefelter syndrome with diagnostic difficulties in molecular interpretation.
Sharma R, Jamwal M, Senee H, Kaur J, Kumar N, Arora A, Gainder S, Ahluwalia J, Das R.
Blood Coagul Fibrinolysis. 2023 Jan 1;34(1):82-83. doi: 10.1097/MBC.0000000000001165. Epub 2022 Aug 30.
PMID:36165062
The status of carrier and prenatal diagnosis of haemophilia in China.
Dai J, Lu Y, Ding Q, Wang H, Xi X, Wang X.
Haemophilia. 2012 Mar;18(2):235-40. doi: 10.1111/j.1365-2516.2011.02630.x. Epub 2011 Sep 12.
PMID:21910785
Hemophilia A: carrier detection and prenatal diagnosis by DNA analysis.
Pecorara M, Casarino L, Mori PG, Morfini M, Mancuso G, Scrivano AM, Boeri E, Molinari AC, De Biasi R, Ciavarella N, et al.
Blood. 1987 Aug;70(2):531-5.
PMID:3111562
Prenatal diagnosis and genetic analysis of novel missense mutation in FVIII gene.
Guo Y, Liu L, Mao B, Xie Z, Tian Q, Zhang C, Ma X.
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2024 Sept 28;49(9):1523-1530. doi: 10.11817/j.issn.1672-7347.2024.230520.
PMID:39931783
The contribution of DNA analysis to carrier detection and prenatal diagnosis of hemophilia A and B.
Bröcker-Vriends AH, Bakker E, Kanhai HH, van Ommen GJ, Reitsma PH, van de Kamp JJ, Briët E.
Ann Hematol. 1992 Jan;64(1):2-11. doi: 10.1007/BF01811464.
PMID:1739755
Carrier detection and prenatal diagnosis of hemophilia A: 5-years experience at a hemophilia center.
Sacchi E, Randi AM, Tagliavacca L, Sampietro M, Primignani P, Mannucci PM.
Int J Clin Lab Res. 1992;21(4):310-3. doi: 10.1007/BF02591668.
PMID:1350470
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