Results 241 to 250 of about 110,198 (324)

Can cell-free fetal DNA screening be utilized for the assessment of chromosomal abnormalities in fetuses with mildly increased nuchal translucency? [PDF]

Arch Gynecol Obstet
Su L, Zhao W, Huang H, Li Y, Xie X, Cai M, Zheng L, Xu L, Wu X.   +8 more
europepmc   +1 more source

Factors affecting parental decisions for termination of pregnancy in the presence of a prenatal trisomy 21 diagnosis. [PDF]

Rev Assoc Med Bras (1992)
Peker A, Tanaçan A, Özen N, İpek G, Okutucu G, Ağaoğlu Z, Çakar EŞ, Şahin D.   +7 more
europepmc   +1 more source

Rapid Detection of Fetal Aneuploidies by Quantitative Fluorescent-Polymerase Chain Reaction for Prenatal Diagnosis in the Turkish Population

Balkan Journal of Medical Genetics, 2012
Guzel A, Yilmaz M, Demirhan O, Pazarbasi A, Kocaturk-Sel S, Erkoc M, Inandiklioglu N, Ozgunen F, Sariturk C   +8 more
doaj   +1 more source

Prenatal Screening for Monosomy X in the First Trimester: A Comparison of a Thai Predictive Model and the Fetal Medicine Foundation Algorithm. [PDF]

Int J Womens Health
Kongsung N, Tongprasert F, Kunanukulwatana C, Tongsong T.   +3 more
europepmc   +1 more source

Trisomy 21 and thyroid dysfunction: A study in a cohort of Sri Lankan children [PDF]

Ashangi Madhushinie Weerasinghe, Navoda Atapattu, S M Chaturika Seneviratne, Ruwangi Dissanayake   +3 more
openalex   +1 more source

Trisomy 8-Associated Intestinal Behcet’s Disease That Achieved Complete Remission With Mesalazine

, 2018
Satoshi Tanida, Keiji Ozeki, Tsutomu Mizoshita, Mamoru Tanika, Hirotada Nishie, Yasuyuki Okamoto, Takaya Shimura, Eiji Kubota, Hiromi Kataoka   +8 more
openalex   +2 more sources

In the era of copy number variation sequencing: changes in the target population for prenatal diagnosis and what is the optimal prenatal diagnostic strategy? [PDF]

Front Med (Lausanne)
Yang S, Li R, Xin S, He Y, Teng S, Gao Y, Fu X.   +6 more
europepmc   +1 more source

Cytogenetic profile of chronic myeloid leukaemia patients resistant to imatinib at tertiary level in Indonesia. [PDF]

Mol Cytogenet
Rinaldi I, Louisa M, Arwanih EY, Adibah FF, Kadharusman MM, Remifta Putra MA, Winston K, Shufiyani YM, Salma RA.   +8 more
europepmc   +1 more source

Genetic etiology and pregnancy outcomes of abnormal fluid accumulation in fetus: A retrospective cohort study. [PDF]

PLoS One
Cai M, Lin N, Su L, Fu M, Huang H, Xu L.
europepmc   +1 more source

Characterizing circulating rare cells in peripheral blood for detecting and monitoring multiple myeloma and precursor states. [PDF]

NPJ Precis Oncol
Shishido SN, Mason J, Kamal M, Setayesh SM, Vora AU, Berrios D, Rueda LYM, Patel K, Manasanch EE, Orlowski RZ, Kuhn P.   +10 more
europepmc   +1 more source