Results 191 to 200 of about 8,284 (304)
Falciform Ligament Laparoscopic Approach for Preperitoneal Ventral Hernia Repair. [PDF]
JSLSDeed JS.
europepmc +1 more source
Totally Umbilical Hemislant Submanifolds Of Lorentzian (A)-Sasakian Manifold
, 2015 Barnali Laha, Arindam Bhattacharyya
openalex +2 more sources
TOTALLY UMBILICAL CR-SUBMANIFOLDS OF KÄHLER MANIFOLDS [PDF]
, 1985 TOSHITAKA TOYONARI, Hiroaki Nemoto
openalex +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT To investigate the correlation between genetic abnormalities and fetal genitourinary (GU) anomalies in Eastern China and to provide assistance for the clinical management of fetuses with different types of GU anomalies. Five hundred forty‐five fetuses with GU anomalies were enrolled, undergoing karyotyping, copy number variation sequencing ...
Jie Liang +6 more
wiley +1 more source
Comparison of Reduced-Port Totally Robotic Pancreaticoduodenectomy with Conventional Totally Robotic and Laparoscopic Pancreaticoduodenectomy. [PDF]
J Clin MedLee B, Han HS, Yoon YS, Lee JS.
europepmc +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken +4 more
wiley +1 more source
Bilateral Inguinal Hernia Repair: Laparoscopic Totally Extraperitoneal Versus Open Lichtenstein. [PDF]
Acta Med LituYosypenko MO +2 more
europepmc +1 more source
Some classification results on totally umbilical proper slant and hemi-slant submanifolds of a nearly Kenmotsu manifold [PDF]
, 2012 Siraj Uddin +3 more
openalex +1 more source
Prenatal Evaluation of RNU4‐2 Variants in Fetuses With Central Nervous System Anomalies
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.ABSTRACT Fetal central nervous system (CNS) anomalies are among the most common congenital malformations, yet the overall prenatal diagnostic yield of current genetic testing remains below 40%. Variants in RNU4‐2, a non‐coding gene encoding the U4 small nuclear RNA (snRNA), have recently been linked to a novel highly recurrent dominant ...
Yiyao Chen +13 more
wiley +1 more source