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Publications by I. van der Laar
Distinctive Phenotypic Abnormalities Associated With Submicroscopic 21q22 Deletion Including DYRK1A
Molecular Syndromology
Genetics
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Phenotypic and Genotypic Variability in Four Males With MECP2 Gene Sequence Aberrations Including a Novel Deletion
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Prenatally Diagnosed Submicroscopic Familial Aberrations at 18p11.32 Without Phenotypic Effect
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Biochemistry
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Interstitial 287 Kb Deletion of 4p16.3 Including FGFRL1 Gene Associated With Language Impairment and Overgrowth
Molecular Cytogenetics
Biochemistry
Molecular Medicine
Genetics
Molecular Biology
Hematological Abnormalities and 22q11.2 Deletion Syndrome
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P53 Downregulates Down Syndrome-Associated DYRK1A Through miR-1246
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A Distinctive Skin Rash Associated With Coronavirus Disease 2019 ?
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Fetal Genitourinary Abnormalities Associated With Oligohydramnios
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Npt2b Deletion Attenuates Hyperphosphatemia Associated With CKD
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Fetal Calcifications Are Associated With Chromosomal Abnormalities
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Multidisciplinary