Results 111 to 120 of about 14,761 (152)

Screening Female Patients With Autonomic Nervous System Imbalance Using the Toho Medical Index Before Tooth Extraction. [PDF]

Cureus
Yamashita K, Yoshimine S, Uto A, Uchino M, Kibe T, Sugimura M.   +5 more
europepmc   +1 more source

Mutations in the Receptor Binding Domain of Severe Acute Respiratory Coronavirus-2 Omicron Variant Spike Protein Significantly Stabilizes Its Conformation. [PDF]

Viruses
Peters MH.
europepmc   +1 more source

<i>F</i>u<i>n</i>Da: scalable serverless data analytics and in situ query processing. [PDF]

J Big Data
Lounissi E, Das SK, Peter R, Zhang X, Ray S, Jia L.   +5 more
europepmc   +1 more source

Correlation between intravesical prostatic protrusion and ejaculatory dysfunction after tamsulosin treatment in men with BPH. [PDF]

World J Urol
Gezmiş CT, Çilesiz NC, Kartal VH, Altan MK, Çakıroğlu B, Balcı MBC.   +5 more
europepmc   +1 more source

Construction and analysis of the execution model for Chinese primary school teachers' extracurricular physical education service teaching: a case study of Henan Province. [PDF]

Front Psychol
Ma T, Wang J, Zhang K, Cao L.
europepmc   +1 more source

Lab-in-Syringe Automated Miniaturized Bioconjugation of Magnetic Beads with Anti-SARS-CoV2 Antibodies. [PDF]

ACS Omega
Svobodova Z, Krizova L, Matejkova N, Smela D, Beranek M, Bilkova Z, Horstkotte B.   +6 more
europepmc   +1 more source

Screening Questions to Identify Low Vision and Acuity-Defined Legal Blindness. [PDF]

Invest Ophthalmol Vis Sci
Wu YH, Yu D, Goldstein J, Kwon M, Wang C, Legge GE.   +5 more
europepmc   +1 more source

Interstitial 1q Deletion Syndrome: A New Patient with Congenital Diaphragmatic Hernia and Multiple Midline Anomalies. [PDF]

Genes (Basel)
Serra G, Nardello R, Antona V, Di Pace MR, Giliberti A, Giuffrè M, Morreale DM, Piro E, Schierz IAM, Sergio M, Valenti G, Pensabene M, Corsello G.   +12 more
europepmc   +1 more source

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Partial trisomy 1 (q42→ter)

Clinical Genetics, 1980
Clinical findings on three closely related, severely malformed infants and a 20‐week‐old fetus with an identical partial trisomy of chromosome 1 (1q42→ter) have made possible the delineation of a new syndrome. The typical manifestations of this syndrome are: severe intrauterine and postnatal developmental retardation, trigonocephaly with wide sutures ...
J. Leisti, P. Aula
openaire   +1 more source

Trisomy (1q) (q42→qter): confirmation of a syndrome

Clinical Genetics, 1988
This paper describes for the first time the clinical findings in a case of pure trisomy (1q)(q42→qter). Eight cases involving this trisomy have been reported previously, but these were complicated by additional chromosomal changes, and hence the assignation of a discrete phenotype remained doubtful.
Chia, N. L., Bousfield, L. R., Poon, C. C.S., Trudinger, B. J.   +3 more
openaire   +3 more sources