The birth defects conferences: the last ten years and the next

The anatomy of the human genome: a neo-Vesalian basis for medicine in the 21st century.

JAMA·2001

The sequence of the human genome.

Science (New York, N.Y.)·2001

Implications of the Human Genome Project for medical science.

JAMA·2001

Overlap of PIV syndrome, VACTERL and Pallister-Hall syndrome: clinical and molecular analysis.

Clinical genetics·2000

Online Mendelian Inheritance in Man (OMIM).

Human mutation·1999

Cloning of multiple keratin 16 genes facilitates prenatal diagnosis of pachyonychia congenita type 1.

Prenatal diagnosis·1999

Limb anomalies from evolutionary, developmental, and genetic perspectives.

Birth defects original article series·1996

Multisite neural tube closure in humans.

Birth defects original article series·1996

Severe arterial hypertension, a silent complication of Williams-Beuren syndrome: A case report with literature review.

Radiology case reports·2026

Cell-of-origin Discovery in Infant Leukemia through Integration of 3D Models and Patient Transcriptomic Data.

Journal of visualized experiments : JoVE·2026

Safety and Efficacy of Amotosalen-Ultraviolet A Pathogen-Reduced Platelets Transfused to Neonates.

Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie·2026

An unanticipated case of congenital high airway obstruction syndrome with type C tracheoesophageal fistula and cerebral ventriculomegaly in a preterm infant - is a small stomach a remote clue?

Case reports in perinatal medicine·2026

Role of Color Doppler and Microvascular Flow Imaging in the Assessment of Mesenteric Lymph Nodes in Pediatric Patients.

Cureus·2026

Impact of the neonatal intensive critical ultrasound workflow for managing neonatal acute pulmonary hypertension.

Frontiers in pediatrics·2026

Related Experiment Videos

The birth defects conferences: the last ten years and the next

Related Concept Videos

The anatomy of the human genome: a neo-Vesalian basis for medicine in the 21st century.

The sequence of the human genome.

Implications of the Human Genome Project for medical science.

Overlap of PIV syndrome, VACTERL and Pallister-Hall syndrome: clinical and molecular analysis.

Online Mendelian Inheritance in Man (OMIM).

Cloning of multiple keratin 16 genes facilitates prenatal diagnosis of pachyonychia congenita type 1.

Limb anomalies from evolutionary, developmental, and genetic perspectives.

Multisite neural tube closure in humans.

Severe arterial hypertension, a silent complication of Williams-Beuren syndrome: A case report with literature review.

Cell-of-origin Discovery in Infant Leukemia through Integration of 3D Models and Patient Transcriptomic Data.

Safety and Efficacy of Amotosalen-Ultraviolet A Pathogen-Reduced Platelets Transfused to Neonates.

An unanticipated case of congenital high airway obstruction syndrome with type C tracheoesophageal fistula and cerebral ventriculomegaly in a preterm infant - is a small stomach a remote clue?

Role of Color Doppler and Microvascular Flow Imaging in the Assessment of Mesenteric Lymph Nodes in Pediatric Patients.

Impact of the neonatal intensive critical ultrasound workflow for managing neonatal acute pulmonary hypertension.

Related Experiment Videos

The birth defects conferences: the last ten years and the next

Related Concept Videos

Related Articles