Results 141 to 150 of about 274,249 (195)

Prenatal molecularly supported diagnosis of a fetus with urinary malformation caused by novel compound heterozygous variants in the <i>FAM149B1</i> gene. [PDF]

Intractable Rare Dis Res
Liu J, Wu Y, Xu S, Qin Y, Li G, Chen Y, Li L, Liu F, Li S, Li N, Wang J.   +10 more
europepmc   +1 more source

Clinico-Pathological Discordance in a Partial Hydatidiform Mole With Coexisting Live Fetus and Subsequent Aggressive Gestational Trophoblastic Neoplasia: A Case Report. [PDF]

Cureus
Turri-Vasquez GA, Eman-Greci GA, Castro-El Fakhri S, Patino-Sepulveda D, Bosque V, Cortes-Charry R.   +5 more
europepmc   +1 more source

Prenatal Etiology Diagnosis of Rare Compound Heterozygous PROC Gene Variants in a Fetus With Ocular Ultrasonic Anomaly Using Whole Exome Sequencing. [PDF]

Mol Genet Genomic Med
Zhuang J, Huang N, Gu L, Fu W.
europepmc   +1 more source

Correction to "Investigation and Care of a Small-for-Gestational-Age Fetus and a Growth Restricted Fetus (Green-top Guideline No. 31)". [PDF]

BJOG
europepmc   +1 more source

A Rare Case of Acardiac Acephalus Fetus in Monochorionic Twins. [PDF]

Cureus
Raman S, Murmu S.
europepmc   +1 more source

The maternal-fetal communicatome: a scoping review and network physiology perspective on a unified, adaptive, and multiscale interaction network. [PDF]

Front Netw Physiol
Lakhno IV.
europepmc   +1 more source