[A case of XX-XY chimerism with normal male phenotype (author's transl)]

Accessory genetic content in Campylobacter jejuni ST21CC isolates from feces and blood.

International journal of medical microbiology : IJMM·2017

First case of human bacteraemia by Catabacter hongkongensis in Scandinavia.

New microbes and new infections·2016

Scanning electron microscopy and epifluorescence investigation of bacterial colonization of marine sand sediments.

Microbial ecology·2013

Two Missense Mutations in the Primary Autosomal Recessive Microcephaly Gene MCPH1 Disrupt the Function of the Highly Conserved N-Terminal BRCT Domain of Microcephalin.

Molecular syndromology·2012

High prevalence of the NBN gene mutation c.657-661del5 in Southeast Germany.

Journal of applied genetics·2010

Imaging of spheres with the confocal scanning optical microscope.

Optics letters·2009

Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas.

Humangenetik·1975

Climate associated variations in the human serum albumin level.

Humangenetik·1975

A technique for in situ karyotyping of primary amniotic fluid cell cultures.

Humangenetik·1975

Sister chromatid exchanges and chromatid interchanges in bloom's syndrome.

Humangenetik·1975

Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

Humangenetik·1975

The Bf locus in the HLA region of chromosome 6: linkage and association studies.

Humangenetik·1975

Signatures of rapid trajectory control during finger and arm movements.

Experimental brain research·2026

Elucidating linear programs by neural encodings.

Frontiers in artificial intelligence·2025

Research on fractional-order memory system signals based on Loop-By-Loop Progressive Iterative Method.

Scientific reports·2024

Solving olympiad geometry without human demonstrations.

Nature·2024

The human inactive X chromosome modulates expression of the active X chromosome.

Cell genomics·2023

"If you got a problem, I got a problem too": working toward making academic science more equitable.

Molecular biology of the cell·2022

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[A case of XX-XY chimerism with normal male phenotype (author's transl)]

Related Concept Videos

Accessory genetic content in Campylobacter jejuni ST21CC isolates from feces and blood.

First case of human bacteraemia by Catabacter hongkongensis in Scandinavia.

Scanning electron microscopy and epifluorescence investigation of bacterial colonization of marine sand sediments.

Two Missense Mutations in the Primary Autosomal Recessive Microcephaly Gene MCPH1 Disrupt the Function of the Highly Conserved N-Terminal BRCT Domain of Microcephalin.

High prevalence of the NBN gene mutation c.657-661del5 in Southeast Germany.

Imaging of spheres with the confocal scanning optical microscope.

Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas.

Climate associated variations in the human serum albumin level.

A technique for in situ karyotyping of primary amniotic fluid cell cultures.

Sister chromatid exchanges and chromatid interchanges in bloom's syndrome.

Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

The Bf locus in the HLA region of chromosome 6: linkage and association studies.

Signatures of rapid trajectory control during finger and arm movements.

Elucidating linear programs by neural encodings.

Research on fractional-order memory system signals based on Loop-By-Loop Progressive Iterative Method.

Solving olympiad geometry without human demonstrations.

The human inactive X chromosome modulates expression of the active X chromosome.

"If you got a problem, I got a problem too": working toward making academic science more equitable.

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[A case of XX-XY chimerism with normal male phenotype (author's transl)]

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