H Malmgren

A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 cases.

François Rousseau, Dominique Heitz, Jack Tarleton et al. · PubMed · 1994 · 294 citations

Capture PCR: efficient amplification of DNA fragments adjacent to a known sequence in human and YAC DNA.

M Lagerström, Jüri Parik, H Malmgren et al. · Genome Research · 1991 · 69 citations · Full text

Specific Oligonucleotide, Genetics, Dna Analysis +20

Single cell CGH analysis reveals a high degree of mosaicism in human embryos from patients with balanced structural chromosome aberrations

H Malmgren · Molecular Human Reproduction · 2002 · 67 citations · Full text

Human Preimplantation Embryos, Cytogenetics, Numerical Aberrations +22

Detailed molecular and clinical characterization of three patients with 21q deletions

Anna Lindstrand, H Malmgren, Sigrid Sahlén et al. · Clinical Genetics · 2009 · 65 citations · Full text

Clinical and molecular consequences of disease-associated de novo mutations in SATB2

Hemant Bengani, Mark T. Handley, Mohsan Alvi et al. · Genetics in Medicine · 2017 · 61 citations · Full text