Genetic polymorphism of the human complement component C'3 among North Germans

Cardiac MRI in restrictive cardiomyopathy.

Clinical radiology·2011

Decoding Substitution Ciphers by Means of Word Matching with Application to OCR.

IEEE transactions on pattern analysis and machine intelligence·2011

Metal Speciation in the ppt Range by HPLC and Diode Laser Atomic Absorption Spectrometry in a Flame.

Analytical chemistry·2011

Construction of oligonucleotide microarrays (biochips) via thioether linkage for the detection of bacterial meningitis.

Bioconjugate chemistry·2009

The murine pan T cell marker CD96 is an adhesion receptor for CD155 and nectin-1.

Biochemical and biophysical research communications·2007

Impact of a comprehensive telephone-based disease management programme on quality-of-life in patients with heart failure.

The National medical journal of India·2007

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

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

Scientific reports·2026

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

The Lancet. Microbe·2026

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

Frontiers in genetics·2026

A Novel <i>FN1</i> Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

Journal of clinical medicine·2026

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

HLA·2026

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Molecular syndromology·2026

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Genetic polymorphism of the human complement component C'3 among North Germans

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Cardiac MRI in restrictive cardiomyopathy.

Decoding Substitution Ciphers by Means of Word Matching with Application to OCR.

Metal Speciation in the ppt Range by HPLC and Diode Laser Atomic Absorption Spectrometry in a Flame.

Construction of oligonucleotide microarrays (biochips) via thioether linkage for the detection of bacterial meningitis.

The murine pan T cell marker CD96 is an adhesion receptor for CD155 and nectin-1.

Impact of a comprehensive telephone-based disease management programme on quality-of-life in patients with heart failure.

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

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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.

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

A Novel <i>FN1</i> Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

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Genetic polymorphism of the human complement component C'3 among North Germans

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