Merel Klaassens

Congenital Diaphragmatic Hernia and Chromosome 15q26: Determination of a Candidate Region by Use of Fluorescent In Situ Hybridization and Array-Based Comparative Genomic Hybridization

Merel Klaassens, Marieke van Dooren, H. J. Eussen et al. · The American Journal of Human Genetics · 2005 · 144 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Genome-wide oligonucleotide-based array comparative genome hybridization analysis of non-isolated congenital diaphragmatic hernia

Daryl A. Scott, Merel Klaassens, Ashley M. Holder et al. · Human Molecular Genetics · 2007 · 83 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A guideline for the clinical management of basal cell naevus syndrome (Gorlin–Goltz syndrome)*

Babette J.A. Verkouteren, B. Cosgun, Marie G.H.C. Reinders et al. · British Journal of Dermatology · 2021 · 65 citations · Full text

Medicine, Dermatology, Oncology +14

Congenital diaphragmatic hernia associated with duplication of 11q23‐qter

Merel Klaassens, Daryl A. Scott, Marieke van Dooren et al. · American Journal of Medical Genetics Part A · 2006 · 54 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Environmental factors in the etiology of esophageal atresia and congenital diaphragmatic hernia: Results of a case‐control study

Janine F. Felix, Marieke F. van Dooren, Merel Klaassens et al. · Birth Defects Research Part A Clinical and Molecular Teratology · 2008 · 51 citations

Public Health, Child Health, Pediatrics +14