M. Barch

发表

Chromosome 20q deletion and progression to monosomy 7 in a patient with Shwachman-Diamond syndrome without MDS/AML.

A. Raj, S. Bertolone, J. Hersh, 2003, Journal of pediatric hematology/oncology.

Partial duplication 4q and deletion 1p36 in monozygotic twins with discordant phenotypes.

B. Angle, G. Gowans, J. Hersh, 2002, American journal of medical genetics.

Estradiol stimulates transcription of nuclear respiratory factor-1 and increases mitochondrial biogenesis.

C. Klinge, N. Wickramasinghe, K. Mattingly, 2008, Molecular endocrinology.

Chapter 1 the cell and cell division

H. Lawce, M. Barch, 2017 .

Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormality

M. Kalff-Suske, P. Williams, H. Kleinert, 1997, Clinical genetics.

Molecular characterization of distal 4q duplication in two patients using oligonucleotide array‐based comparative genomic hybridization (oaCGH) analysis

A. Asamoah, G. Gowans, Kathryn Platky, 2014, American journal of medical genetics. Part A.

De novo 1;10 balanced translocation in an infant with thanatophoric dysplasia: a clue to the locus of the candidate gene.

J. Roberts, S. Peiper, J. Hersh, 1995, Journal of medical genetics.

The AGT cytogenics laboratory manual

T. Knutsen, J. Spurbeck, M. Barch, 1997 .

Identification of trisomy 16 murine embryos by fluorescence in situ hybridization.

M. Pisano, R. Greene, P. Nugent, 2001, BioTechniques.