[Two subterminal heterochromatin regions in a rare form of 21-21 translocation]

Intra-population variability of ocean acidification impacts on the physiology of Baltic blue mussels (Mytilus edulis): integrating tissue and organism response.

Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology·2016

Extra-adrenal pheochromocytoma in the organ of Zuckerkandl: diagnosis and treatment strategies.

Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association·2011

["Ultrasound tonsillectomy" in comparison with conventional tonsillectomy].

HNO·2002

Separation of human pancreatic carboxypeptidase A isoenzymes by high performance liquid chromatography.

Biomedical chromatography : BMC·1993

[Evaluation of the immunomagnetic beads separation technique as a routine method for HLA typing].

Beitrage zur Infusionstherapie = Contributions to infusion therapy·1990

[Immunotherapy following habitual abortion in paternal chromosome translocation].

Geburtshilfe und Frauenheilkunde·1989

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

Chromosome-Scale Assembly of Novel Caenorhabditis sp. 65 (strain JU4118).

microPublication biology·2026

Comparative analysis of chromosome interaction networks in 12 human cell types using Hi-C.

Yi chuan = Hereditas·2026

Interobserver reliability and digital morphometric characterization of constitutional chromosomal heteromorphisms in clinical cytogenetics.

Human genetics·2026

Functional Validation of a CC2D2A Non-Canonical Splice-Site Variant Supports Prenatal Molecular Testing in Joubert Syndrome.

Diagnostics (Basel, Switzerland)·2026

Overcoming the nuclear barrier in nonviral gene therapy: mechanisms, carrier design, and translational perspectives on NLS peptide and DNA targeting sequence strategies.

Drug delivery·2026

Structural defects in male meiotic cell division lead to reproductive genome instability and disturbed microsporogenesis in banana (Musa spp.).

Frontiers in plant science·2026

Related Experiment Videos

[Two subterminal heterochromatin regions in a rare form of 21-21 translocation]

Related Concept Videos

Intra-population variability of ocean acidification impacts on the physiology of Baltic blue mussels (Mytilus edulis): integrating tissue and organism response.

Extra-adrenal pheochromocytoma in the organ of Zuckerkandl: diagnosis and treatment strategies.

["Ultrasound tonsillectomy" in comparison with conventional tonsillectomy].

Separation of human pancreatic carboxypeptidase A isoenzymes by high performance liquid chromatography.

[Evaluation of the immunomagnetic beads separation technique as a routine method for HLA typing].

[Immunotherapy following habitual abortion in paternal chromosome translocation].

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.

Chromosome-Scale Assembly of Novel Caenorhabditis sp. 65 (strain JU4118).

Comparative analysis of chromosome interaction networks in 12 human cell types using Hi-C.

Interobserver reliability and digital morphometric characterization of constitutional chromosomal heteromorphisms in clinical cytogenetics.

Functional Validation of a CC2D2A Non-Canonical Splice-Site Variant Supports Prenatal Molecular Testing in Joubert Syndrome.

Overcoming the nuclear barrier in nonviral gene therapy: mechanisms, carrier design, and translational perspectives on NLS peptide and DNA targeting sequence strategies.

Structural defects in male meiotic cell division lead to reproductive genome instability and disturbed microsporogenesis in banana (Musa spp.).

Related Experiment Videos

[Two subterminal heterochromatin regions in a rare form of 21-21 translocation]

Related Concept Videos

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