[Encounter with syndromes, genetics and geneticists]

Polytopic anomalies with agenesis of the lower vertebral column.

American journal of medical genetics·1999

Salivary gland disorders and heredity.

American journal of medical genetics·1997

Unusual complex of ventral midline anomalies: a multiple congenital anomalies/mental retardation syndrome.

American journal of medical genetics·1996

Blepharo-cheilo-dontic (BCD) syndrome.

American journal of medical genetics·1996

Stüve-Wiedemann syndrome: update and historical footnote.

American journal of medical genetics·1996

[Neonatal progeroid syndrome (Wiedemann-Rautenstrauch). A follow-up study].

Klinische Padiatrie·1994

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

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

Neuroborreliosis in children: Focus on ischemic stroke-a case report and literature review.

Klinische Padiatrie·2026

Changes in Mamillopontine Distance and Pontomesencephalic angle following Treatment for Pediatric Idiopathic Intracranial Hypertension.

Klinische Padiatrie·2026

Guidance for the Diagnosis and Treatment of Rare Embryonal and Sarcomatous Brain Tumors-a Report from the Central Nervous System-International Registry for Rare Embryonal and Sarcomatous Tumors German Society of Pediatric Oncology and Hematology Study Group.

Klinische Padiatrie·2026

Single-Cell Transcriptional States of Human Leukocyte Antigen DR Positive CD4 Positive T Cells Linked to Genetic Susceptibility of Gastric Cancer.

Immunological investigations·2026

Correction: GWAS analysis of a depression cohort defined by an EHR-phenotyping algorithm reveals the role of immune regulations in depression risk.

Frontiers in genetics·2026

Optical genome mapping enhanced by refined variant interpretation in pediatric acute lymphoblastic leukemia.

The Journal of pathology·2026

GHT-SELEX demonstrates unexpectedly high intrinsic sequence specificity and complex DNA binding of many human transcription factors.

Nature methods·2026

Dual SGLT1/2 inhibition with sotagliflozin improves cardiac function and metabolism in type 2 diabetic mice.

npj metabolic health and disease·2026

An expanded codebook of human transcription factor DNA-binding specificity.

Nature·2026

Related Experiment Videos

[Encounter with syndromes, genetics and geneticists]

Related Concept Videos

Polytopic anomalies with agenesis of the lower vertebral column.

Salivary gland disorders and heredity.

Unusual complex of ventral midline anomalies: a multiple congenital anomalies/mental retardation syndrome.

Blepharo-cheilo-dontic (BCD) syndrome.

Stüve-Wiedemann syndrome: update and historical footnote.

[Neonatal progeroid syndrome (Wiedemann-Rautenstrauch). A follow-up study].

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

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].

Neuroborreliosis in children: Focus on ischemic stroke-a case report and literature review.

Changes in Mamillopontine Distance and Pontomesencephalic angle following Treatment for Pediatric Idiopathic Intracranial Hypertension.

Guidance for the Diagnosis and Treatment of Rare Embryonal and Sarcomatous Brain Tumors-a Report from the Central Nervous System-International Registry for Rare Embryonal and Sarcomatous Tumors German Society of Pediatric Oncology and Hematology Study Group.

Single-Cell Transcriptional States of Human Leukocyte Antigen DR Positive CD4 Positive T Cells Linked to Genetic Susceptibility of Gastric Cancer.

Correction: GWAS analysis of a depression cohort defined by an EHR-phenotyping algorithm reveals the role of immune regulations in depression risk.

Optical genome mapping enhanced by refined variant interpretation in pediatric acute lymphoblastic leukemia.

GHT-SELEX demonstrates unexpectedly high intrinsic sequence specificity and complex DNA binding of many human transcription factors.

Dual SGLT1/2 inhibition with sotagliflozin improves cardiac function and metabolism in type 2 diabetic mice.

An expanded codebook of human transcription factor DNA-binding specificity.

Related Experiment Videos

[Encounter with syndromes, genetics and geneticists]

Related Concept Videos

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