[Myopathia distalis infantilis hereditaria? 1st communication (author's transl)]

CR-EST: a resource for crop ESTs.

Nucleic acids research·2004

[Siblings with neonatal progeroid syndrome (Wiedemann-Rautenstrauch)].

Klinische Padiatrie·2004

[Noonan's syndrome with an unusual combination of hypertrophic cardiomyopathy, congenital bicuspid aortic valve, coarctation of the aorta and hypoplastic aortic arch].

Zeitschrift fur Kardiologie·2004

[Neonatal progeroid syndrome (Wiedemann-Rautenstrauch syndrome): case report and review of the literature].

Klinische Padiatrie·2000

Syndrome of autosomal recessive polycystic kidneys with skeletal and facial anomalies is not linked to the ARPKD gene locus on chromosome 6p.

American journal of medical genetics·1999

A previously unrecognised phenotype characterised by obesity, muscular hypotonia, and ability to speak in patients with Angelman syndrome caused by an imprinting defect.

European journal of human genetics : EJHG·1999

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

Role of intraoperative ultrasonography as a method of neuro-navigation in surgical treatment of intracranial hemorrhage.

Surgical neurology international·2026

Correction: Impact of immune function and white matter integrity on cognitive function in patients with bipolar disorder.

Frontiers in immunology·2026

Nomogram combining clinical and ultrasonographic features for differentiating granulomatous lobular mastitis from invasive lobular carcinoma.

Frontiers in oncology·2026

Role of HMGB1 in Neuroinflammation.

Molecular neurobiology·2026

Inborn Errors of Immunity and Hematopoietic Cell Transplantation: Recognition and Pretransplant Management.

Pediatric annals·2026

IL-13 ameliorates hepatocellular steatosis via IL-13Rα1/JNK/FOSL2 signaling pathway.

Cellular and molecular gastroenterology and hepatology·2026

Related Experiment Videos

[Myopathia distalis infantilis hereditaria? 1st communication (author's transl)]

Related Concept Videos

CR-EST: a resource for crop ESTs.

[Siblings with neonatal progeroid syndrome (Wiedemann-Rautenstrauch)].

[Noonan's syndrome with an unusual combination of hypertrophic cardiomyopathy, congenital bicuspid aortic valve, coarctation of the aorta and hypoplastic aortic arch].

[Neonatal progeroid syndrome (Wiedemann-Rautenstrauch syndrome): case report and review of the literature].

Syndrome of autosomal recessive polycystic kidneys with skeletal and facial anomalies is not linked to the ARPKD gene locus on chromosome 6p.

A previously unrecognised phenotype characterised by obesity, muscular hypotonia, and ability to speak in patients with Angelman syndrome caused by an imprinting defect.

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.

Role of intraoperative ultrasonography as a method of neuro-navigation in surgical treatment of intracranial hemorrhage.

Correction: Impact of immune function and white matter integrity on cognitive function in patients with bipolar disorder.

Nomogram combining clinical and ultrasonographic features for differentiating granulomatous lobular mastitis from invasive lobular carcinoma.

Role of HMGB1 in Neuroinflammation.

Inborn Errors of Immunity and Hematopoietic Cell Transplantation: Recognition and Pretransplant Management.

IL-13 ameliorates hepatocellular steatosis via IL-13Rα1/JNK/FOSL2 signaling pathway.

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[Myopathia distalis infantilis hereditaria? 1st communication (author's transl)]

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