G. Hamers

发表

Distribution of meiotic recombination along nondisjunction chromosomes 21 in Down syndrome determined using cytogenetics and RFLP haplotyping

J. Geraedts, R. Jongbloed, H. Meijer, 1989, Human Genetics.

Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer-Giedion syndrome.

E. Haan, M. Wagner, M. Frydman, 1995, Human molecular genetics.

Marker chromosome identification by micro‐FISH

J. Geraedts, U. Moog, J. Engelen, 1996, Clinical genetics.

Translocation t(2;3)(p15–23;q26–27) in myeloid malignancies: report of 21 new cases, clinical, cytogenetic and molecular genetic features

F. Speleman, A. Hagemeijer, L. Michaux, 2004, Leukemia.

ICF syndrome: a new case and review of the literature

D. Smeets, U. Moog, G. Merkx, 1994, Human Genetics.

Subfertile men with constitutive chromosome abnormalities do not necessarily refrain from intracytoplasmic sperm injection treatment: a follow-up study on 75 Dutch patients.

J. Giltay, J. Kremer, R. Hordijk, 1999, Human reproduction.

Characterization of a de novo unbalanced translocation t(14q18q) using microdissection and fluorescence in situ hybridization.

A. Plomp, J. Geraedts, J. Vles, 1998, American journal of medical genetics.

Detection of a cryptic translocation t(13;20)(q34;p13) in an unexplained case of MCA/MR: value of FISH over high resolution banding.

C. D. de Die-Smulders, J. Engelen, J. Albrechts, 1999, American journal of medical genetics.

A simple and efficient method for microdissection and microFISH.

J. Geraedts, J. Engelen, J. Albrechts, 1998, Journal of medical genetics.

Multiplex ligation dependent probe amplification (MLPA) for rapid distinction between unique sequence positive and negative marker chromosomes in prenatal diagnosis

R. Galjaard, M. Srebniak, D. Van Opstal, 2011, Molecular Cytogenetics.

Human parvovirus B19 infection and unbalanced translocation in a case of hydrops fetalis

C. D. de Die-Smulders, C. Willekes, F. Roumen, 1994, Prenatal diagnosis.