[Gonadal dysgenesis with X-isochromosome of paternal origin (author's transl)]

High-precision measurement of the W boson mass with the CDF II detector.

Science (New York, N.Y.)·2022

Search for the Exotic Meson X(5568) with the Collider Detector at Fermilab.

Physical review letters·2018

Combined Forward-Backward Asymmetry Measurements in Top-Antitop Quark Production at the Tevatron.

Physical review letters·2018

Tevatron Combination of Single-Top-Quark Cross Sections and Determination of the Magnitude of the Cabibbo-Kobayashi-Maskawa Matrix Element V_{tb}.

Physical review letters·2015

Search for Resonances Decaying to Top and Bottom Quarks with the CDF Experiment.

Physical review letters·2015

Tevatron constraints on models of the Higgs boson with exotic spin and parity using decays to bottom-antibottom quark pairs.

Physical review letters·2015

[The Gap between Need and Reality in Neuropsychological Care in Pediatric Oncology - Position Paper].

Klinische Padiatrie·2026

BK Virus Associated Hemorrhagic Cystitis in Pediatric Hematopoietic Stem Cell Transplantation Recipients: A Retrospective Analysis.

Klinische Padiatrie·2026

Clinical phenotypes and household structure in pediatric invasive meningococcal disease: A retrospective cohort study.

Klinische Padiatrie·2026

Surgery in the Neonatal Intensive Care Unit: Current Practices and Perspectives of Pediatric Surgeons in Germany.

Klinische Padiatrie·2026

PTCH1-Related Gorlin Syndrome: Expanding the Clinical and Molecular Spectrum in a Cohort of 11 Patients.

Klinische Padiatrie·2026

[Parental satisfaction with home monitoring in children with complex congenital heart diseases (CCHD): A cross-sectional study].

Klinische Padiatrie·2026

Genotype-phenotypic correlation in a Chinese patient with isolated lissencephaly sequence caused by 17p13.3p13.2 chromosomal microdeletion: a 6-year follow-up study.

Frontiers in genetics·2026

GRIA3 Duplication at Xq25 in a Young Adult Male With Profound Intellectual Disability and Morbid Obesity: A Case Report.

Case reports in genetics·2026

Leveraging Long-Read Sequencing to Bridge the Diagnostic and Equity Gaps in Differences of Sex Development (DSD).

The Journal of clinical endocrinology and metabolism·2026

Progenitor Timing Shapes NG2-Glia Fate and Oligodendrocyte Differentiation.

Glia·2026

Fraternal Birth Order Effect and Other Sibship Effects in Bisexual and Asexual Men and Women.

Archives of sexual behavior·2026

Correlation analysis of cognitive dysfunction and fluctuations in serum fibroblast growth factor 21 (FGF21) levels in the overweight group.

Journal of medical biochemistry·2026

Related Experiment Videos

[Gonadal dysgenesis with X-isochromosome of paternal origin (author's transl)]

Related Concept Videos

High-precision measurement of the W boson mass with the CDF II detector.

Search for the Exotic Meson X(5568) with the Collider Detector at Fermilab.

Combined Forward-Backward Asymmetry Measurements in Top-Antitop Quark Production at the Tevatron.

Tevatron Combination of Single-Top-Quark Cross Sections and Determination of the Magnitude of the Cabibbo-Kobayashi-Maskawa Matrix Element V_{tb}.

Search for Resonances Decaying to Top and Bottom Quarks with the CDF Experiment.

Tevatron constraints on models of the Higgs boson with exotic spin and parity using decays to bottom-antibottom quark pairs.

[The Gap between Need and Reality in Neuropsychological Care in Pediatric Oncology - Position Paper].

BK Virus Associated Hemorrhagic Cystitis in Pediatric Hematopoietic Stem Cell Transplantation Recipients: A Retrospective Analysis.

Clinical phenotypes and household structure in pediatric invasive meningococcal disease: A retrospective cohort study.

Surgery in the Neonatal Intensive Care Unit: Current Practices and Perspectives of Pediatric Surgeons in Germany.

PTCH1-Related Gorlin Syndrome: Expanding the Clinical and Molecular Spectrum in a Cohort of 11 Patients.

[Parental satisfaction with home monitoring in children with complex congenital heart diseases (CCHD): A cross-sectional study].

Genotype-phenotypic correlation in a Chinese patient with isolated lissencephaly sequence caused by 17p13.3p13.2 chromosomal microdeletion: a 6-year follow-up study.

GRIA3 Duplication at Xq25 in a Young Adult Male With Profound Intellectual Disability and Morbid Obesity: A Case Report.

Leveraging Long-Read Sequencing to Bridge the Diagnostic and Equity Gaps in Differences of Sex Development (DSD).

Progenitor Timing Shapes NG2-Glia Fate and Oligodendrocyte Differentiation.

Fraternal Birth Order Effect and Other Sibship Effects in Bisexual and Asexual Men and Women.

Correlation analysis of cognitive dysfunction and fluctuations in serum fibroblast growth factor 21 (FGF21) levels in the overweight group.

Related Experiment Videos

[Gonadal dysgenesis with X-isochromosome of paternal origin (author's transl)]

Related Concept Videos

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