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Publications by M P Mulder

Recurrence of DiGeorge Syndrome: Prenatal Detection by FISH of a Molecular 22q11 Deletion.

Journal of Medical Genetics

English

Related publications

The Evaluation of DiGeorge Syndrome Gene Deletion Using Molecular Cytogenetic Techniques

English

22q11 Deletion Syndrome: A Genetic Subtype of Schizophrenia

Biological Psychiatry

Biological Psychiatry

English

Interstitial 22q11 Microdeletion Excluding the ADU Breakpoint in a Patient With DiGeorge Syndrome

Human Molecular Genetics

Molecular Biology

English

DiGeorge Syndrome (Chromosome 22q11.2 Deletion Syndrome): A Historical Perspective With Review of 66 Patients

Journal of Surgery and Medicine

English

Movement Disorders in Adults With 22q11 Deletion Syndrome

Movement Disorders Clinical Practice

English

Der(22) Syndrome and Velo-Cardio-Facial Syndrome/DiGeorge Syndrome Share a 1.5-Mb Region of Overlap on Chromosome 22q11

American Journal of Human Genetics

English

Sleep Patterns and Problems Among Children With 22q11 Deletion Syndrome

Molecular genetics & genomic medicine

Molecular Biology

English

Lower Prepulse Inhibition in Children With the 22q11 Deletion Syndrome

American Journal of Psychiatry

English

Array CGH Analysis Reveals Deletion of Chromosome 22q11 in CLL With Normal Karyotype and No Fish Alterations

British Journal of Haematology

English