Michael G. Brown

发表

Lymphoblasts Reflects Normal Checkpoint Function Induced G2/M Arrest in Group C Fanconi Anemia -

A. J. Zigler, M. Grompe, R. Magenis, 2013 .

Mosaicism of proximal 15q duplication/deletion resulting in Prader–Willi syndrome with normal methylation

R. Magenis, H. Lawce, N. Unsworth, 2005, American journal of medical genetics. Part A.

Meiotic exchange event within the stalk region of an inverted chromosome 22 results in a recombinant chromosome with duplication of the distal long arm

J. Gilhooly, R. Magenis, H. Lawce, 2005, American journal of medical genetics. Part A.

Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: specific regions, extent of deletions, parental origin, and clinical consequences.

J. Zonana, S. Lafranchi, R. Magenis, 1990, American journal of medical genetics.

Is Angelman syndrome an alternate result of del(15)(q11q13)?

D. Ledbetter, J. Opitz, S. Lafranchi, 1987, American journal of medical genetics.

Y‐derived sequences detected in a 45,X male by in situ hybridization

J. Opitz, R. Magenis, J. F. Reynolds, 1987, American journal of medical genetics.

Clinical outcomes of four patients with microdeletion in the long arm of chromosome 2.

S. Olson, J. Reiss, R. Magenis, 1998, American journal of medical genetics.

Cytogenetics: an overview

H. Lawce, M. Brown, Michael G. Brown, 2017 .

Peripheral blood cytogenetic methods

H. Lawce, Michael G. Brown, M. Brown, 2017 .