Results 291 to 300 of about 140,678 (408)

The fetal neurologist: Strategies to improve training, practice, and clinical care

Developmental Medicine &Child Neurology, EarlyView.
Abstract Fetal neurology addresses counselling parents on the clinical significance of brain anomalies encountered in their fetus, including disruptive lesions (i.e. stroke, periventricular haemorrhagic infarction, and infection), and genetically based cortical (i.e.
Tally Lerman‐Sagie, Anthony R. Hart
wiley   +1 more source

Clinical application of chromosome microarray analysis and karyotyping in prenatal diagnosis in Northwest China. [PDF]

Front Genet
Xue S, Liu Y, Wang L, Zhang L, Chang B, Ding G, Dai P.   +6 more
europepmc   +1 more source

Four Karyotypes of Rumex acetosa L.

, 1971
Masahide KURITA, Yûzô Kuroki
openalex   +2 more sources

Genetic Landscape and Risk Stratification of AML With Hyperdiploid Karyotype

European Journal of Haematology, EarlyView.
ABSTRACT Hyperdiploid karyotype (HK) (49–65 chromosomes) in acute myeloid leukemia (AML) is rare. Recently, HK‐AML with only numerical changes has been reclassified into an intermediate risk group in the updated 2022 European LeukemiaNet (ELN) risk classification, which has historically been classified into an adverse risk group.
Ehsan Bahrami Hezaveh, Jiong Yan, Davidson Zhao, Collins Wangulu, Winnie Lo, Cuihong Wei, Hong Chang   +6 more
wiley   +1 more source

Real-time genomic characterization of pediatric acute leukemia using adaptive sampling. [PDF]

Leukemia
Geyer J, Opoku KB, Lin J, Ramkissoon L, Mullighan C, Bhakta N, Alexander TB, Wang JR.   +7 more
europepmc   +1 more source

A Biosystematic Study of Triteleia (Liliaceae). II. Chromosome Numbers and Karyotypes of the Species of Section Calliprora

, 1976
Lee Lenz
openalex   +2 more sources

Myeloid Neoplasms With Erythroid Predominance and Excess Blasts in Young Adults Exhibit Distinct Genetic Profiles

European Journal of Haematology, EarlyView.
ABSTRACT The evolution of acute myeloid leukemia (AML) classifications has progressively shifted the diagnostic focus toward genetic criteria. Nevertheless, morphology remains a key element in clinical practice, often serving as the initial trigger for additional molecular investigations. The diagnosis of acute erythroleukemia (AEML), initially defined
Laurène Fenwarth, Benjamin Podvin, Loïc Vasseur, Delphine Lebon, Guillaume Couillez, Céline Berthon, Alexis Caulier, Elise Fournier, Claire Bories, Benjamin Carpentier, Sabine Tricot, Kevin‐James Wattebled, Catherine Roche‐Lestienne, Valentin Lestringant, Carine Hauspie, Karine Celli‐Lebras, Maël Heiblig, Hervé Dombret, Raphael Itzykson, Jean‐Pierre Marolleau, Loïc Garçon, Claude Preudhomme, Nicolas Duployez, Thomas Boyer   +23 more
wiley   +1 more source

Is intermediate risk really intermediate? Comparison of karyotype and non-invasive prenatal testing results of pregnancies at intermediate risk of trisomy 21 on maternal serum screening. [PDF]

J Genet Couns
Alkan Bulbul G, Kirtis E, Kandemir H, Sanhal CY, Yakut Uzuner S, Karauzum SB, Mendilcioglu II.   +6 more
europepmc   +1 more source

A new hematologic syndrome with a distinct karyotype: the 5 q-- chromosome

, 1975
G. Sokal, Jl. Michaux, Herman Van den Berghe, A. Cordier, J Rodhain, A Ferrant, M Moriau, Marc De Bruyère, J. Sonnet   +8 more
openalex   +1 more source