M. Sutcliffe

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Reverse Genetic Approaches to Cloning Deafness Genes a

K. Steel, S. D. Brown, K. A. Brown, 1991, Annals of the New York Academy of Sciences.

Spermatogenesis in XY, XYSxra and XOSxra mice: A quantitative analysis of spermatogenesis throughout puberty

M. Sutcliffe, P. Burgoyne, S. Darling, 1991, Molecular reproduction and development.

Hepatosplenic γ/δ T-cell lymphoma with isochromosome 7q, translocation t(7;21), and tetrasomy 8 in a 9-year-old girl

M. Sutcliffe, H. Rossbach, W. Chamizo, 2002 .

Analysis of the testes of H-Y negative XOSxrb mice suggests that the spermatogenesis gene (Spy) acts during the differentiation of the A spermatogonia.

M. Sutcliffe, P. Burgoyne, 1989, Development.

Close linkage of the olfactory marker protein gene to the mouse deafness mutation shaker-1.

K. Steel, M. Sutcliffe, S. Brown, 1992, Genomics.

Fertility in mice requires X-Y pairing and a Y-chromosomal “Spermiogenesis” gene mapping to the long arm

M. Sutcliffe, S. Mahadevaiah, P. Burgoyne, 1992, Cell.

Fanconi anemia in brothers initially diagnosed with VACTERL association with hydrocephalus, and subsequently with Baller-Gerold syndrome.

A. Rossi, M. Sutcliffe, H. Rossbach, 1996, American journal of medical genetics.

Translocation breakpoint in two unrelated Tourette syndrome cases, within a region previously linked to the disorder

R. Hauser, M. Mullan, F. Crawford, 2003, Human Genetics.

Monosomy 6q1: syndrome delineation.

B. Kousseff, M. Sutcliffe, J. Hartsfield, 1996, American journal of medical genetics.

The role of unpaired sex chromosomes in spermatogenic failure *

M. Sutcliffe, S. Mahadevaiah, P. Burgoyne, 2009, Andrologia.

Composite adrenal anaplastic neuroblastoma and virilizing adrenocortical tumor with germline TP53 R248W mutation

M. Sutcliffe, H. Rossbach, C. Tebbi, 2008, Pediatric blood & cancer.

A case study of “disorganized development” and its possible relevance to genetic determinants of aging

P. Kruk, J. Shay, R. Walker, 2009, Mechanisms of Ageing and Development.

Uniparental isodisomy of chromosome 14 in two cases: an abnormal child and a normal adult.

V. P. Johnson, P. Papenhausen, B. Kousseff, 1996, American journal of medical genetics.

Uniparental isodisomy of chromosome 14 in two cases: an abnormal child and a normal adult.

V. P. Johnson, P. Papenhausen, B. Kousseff, 1995, American journal of medical genetics.

Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant?

N. Spinner, L. Gaunt, Yiping Shen, 2010, European journal of medical genetics.

Twin–twin transfusion syndrome in a dizygotic monochorionic–diamniotic twin pregnancy

E. Gilbert-Barness, R. Quintero, P. Papenhausen, 2003, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Three cell line mosaicism involving structural and numerical abnormalities of chromosome 18 in a 3.5-year-old girl: 47,XX,+18/47,XX,+del(18)(q22)/46,XX.

B. Kousseff, M. Sutcliffe, O. Mueller, 2001, American journal of medical genetics.

Chromosome 3p25 deletion in mother and daughter with minimal phenotypic effect

B. Kousseff, K. Rauen, M. Sutcliffe, 2006, American journal of medical genetics. Part A.

A patient with an interstitial duplication of chromosome 5p11-p13.3 further confirming a critical region for 5p duplication syndrome.

M. Sutcliffe, M. Loscalzo, T. Becker, 2008, European journal of medical genetics.

Mouse chromosome 7

A. Saunders, J. Peters, M. Sutcliffe, 2004, Mammalian Genome.

EXTREME VARIANT OF ENLARGED HETEROCHROMATIN REGION ON CHROMOSOME 9Q IN A NORMAL CHILD AND MULTIPLE FAMILY MEMBERS

E. Gilbert-Barness, M. Sutcliffe, T. Steffensen, 2009, Fetal and pediatric pathology.

Hepatosplenic gamma/delta T-cell lymphoma with isochromosome 7q, translocation t(7;21), and tetrasomy 8 in a 9-year-old girl.

M. Sutcliffe, H. Rossbach, W. Chamizo, 2002, Journal of pediatric hematology/oncology.

Pre‐B Acute Lymphoblastic Leukemia in a 3‐Year-Old Boy With Pre‐Acute Myelogenous Leukemia Myelodysplastic Syndrome: Cytogenetic Evidence of Common Early Progenitor Cell Ontogeny

M. Sutcliffe, H. Rossbach, J. Barbosa, 1998, Journal of pediatric hematology/oncology.

Construction of a mouse yeast artificial chromosome library in a recombination–deficient strain of yeast

P. Mileham, M. Sutcliffe, S. Brown, 1992, Nature Genetics.

Specific extra chromosomes occur in a modal number dependent pattern in pediatric acute lymphoblastic leukemia

S. Raimondi, James R. Anderson, W. Sanger, 2007, Genes, chromosomes & cancer.

Cytogenetic findings in rare pediatric tumors: Report of a case of interdigitating reticulum cell sarcoma and a case of pancreatoblastoma

M. Sutcliffe, W. Chamizo, J. McFarland, 1995 .