Results 181 to 190 of about 73,620 (322)
Abstract We explored the diversification of the south‐eastern and eastern European Euphorbia agraria s.l. applying molecular (amplified fragment length polymorphism [AFLP] fingerprinting and sequencing of the nuclear ribosomal internal transcribed spacer [ITS]), cytogenetic (relative genome size [RGS] estimations) and morphometric methods.
Naim Berisha+2 more
wiley +1 more source
Correction to: Anifrolumab in Monogenic Lupus caused by TREX1 Mutation. [PDF]
Moran-Alvarez P+6 more
europepmc +1 more source
Some cytogenetic aspects of maize monoploids and monoploid derivatives
Leola E. Ford
openalex +2 more sources
Distinct lineages of the grasshopper Chorthippus parallelus (Orthoptera: Acrididae) form a well‐known hybrid zone (HZ) in the Pyrenees mountain range; the Iberian endemism C. p. erythropus (Cpe) and the subspecies C. p. parallelus, (Cpp) widely distributed throughout the rest of Europe. Both subspecies differ in diverse traits, including the strains of
Patricia Jiménez‐Florido+4 more
wiley +1 more source
Interventional oncology in children: Where are we now?
Abstract Paediatric Interventional Oncology (IO) lags behind adult IO due to a scarcity of specific outcome data. The suboptimal way to evolve this field is relying heavily on adult experiences. The distinct tumour types prevalent in children, such as extracranial germ cell tumours, sarcomas, and neuroblastoma, differ strongly from those found in ...
Premal Amrishkumar Patel+1 more
wiley +1 more source
Genomic technologies and the diagnosis of 46, XY differences of sex development
Abstract Differences/disorders of sex development can be caused by disruptions to the molecular and cellular mechanisms that control development and sex determination of the reproductive organs with 1:100 live births affected. Multiple genes are associated with 46, XY differences/disorders of sex development that can cause varying clinical phenotypes ...
Firman Idris+2 more
wiley +1 more source
Abstract Background Current guidelines indicate that patients with extreme oligozoospermia or azoospermia should be tested for chromosomal imbalances, azoospermia factor (AZF) deletions and/or CFTR variants. For other sperm abnormalities, no genetic diagnostics are recommended.
Manon S. Oud+12 more
wiley +1 more source