D. Dyke

发表

Prenatal diagnosis of 22q11.2 deletion when ultrasound examination reveals a heart defect

A. Wiktor, J. Roberson, S. Manji, 2001, Genetics in Medicine.

Loss of 18q predicts poor survival of patients with squamous cell carcinoma of the head and neck.

R. Zarbo, T. Carey, B. Rybicki, 1998, Genes, chromosomes & cancer.

Diagnostic Testing: A Cost Analysis for Prader-Willi and Angelman Syndromes

D. Dyke, 2006 .

Malformation syndrome of duplication 12q24.1→qter

J. Opitz, L. Weiss, D. Dyke, 1981 .

Location of the X inactivation center in primates and other mammals

L. Weiss, W. Flejter, D. Dyke, 1986, Human Genetics.

The centromere index and relative length of human high-resolution G-banded chromosomes

L. Weiss, M. Worsham, D. Dyke, 1986, Human Genetics.

Translocation(X;Y)(p22.33;p11.2) in XX males: Etiology of male phenotype

R. Magenis, E. Lovrien, L. Allen, 2004, Human Genetics.

Trisomy 13 in patients with hematological malignancies

S. Kaufmann, M. Litzow, R. Pruthi, 2007 .

Isochromosome 5p mosaicism at prenatal diagnosis: observations and outcomes in six cases at chorionic villus sampling and one at amniocentesis

R. Gardner, S. Wilson, A. Daniel, 2002, Prenatal diagnosis.

FISH analysis helps identify low-level mosaicism in Ullrich-Turner syndrome patients

A. Wiktor, D. Dyke, 2004, Genetics in Medicine.

Deletions in Xq26.3–q27.3 including FMR1 result in a severe phenotype in a male and variable phenotypes in females depending upon the X inactivation pattern

S. Schwartz, H. Willard, L. Weiss, 1997, Human Genetics.

Allelic Loss and Tumor Pathology in Head and Neck Squamous Cell Carcinoma

R. Zarbo, B. Rybicki, M. Benninger, 2003, Modern Pathology.

Ring chromosome 6: Case report and review of literature

L. Weiss, K. R. Kini, D. Dyke, 2004, Human Genetics.

Diagnostic testing for Prader-Willi syndrome and Angelman syndrome: A cost comparison

K. Monaghan, A. Wiktor, D. Dyke, 2002, Genetics in Medicine.

Establishment and characterization of UM-EC-2, a tamoxifen-sensitive, estrogen receptor-negative human endometrial carcinoma cell line.

S. Grénman, T. Carey, J. Roberts, 1990, Gynecologic oncology.

Asymmetric skeletal anomalies in siblings

L. Weiss, D. Dyke, S. Ruby, 1984, Clinical genetics.

A prospective study of 92 bladder cancer patients: Cytogenetics, histopathology, and tumor behavior

B. Miles, L. Weiss, J. Crissman, 1989 .

Culture and karyotyping of amniotic fluid cells

L. Weiss, M. Worsham, D. Dyke, 1980 .

Parental age, and how extra isochromosomes (secondary trisomy) arise

L. Weiss, D. Dyke, V. Babu, 1987, Clinical genetics.

Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNA.

S. Schwartz, H. Willard, W. Earnshaw, 1997, Human molecular genetics.

Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype–phenotype correlations

L. Shaffer, S. Patil, C. Jackson-Cook, 2000, Prenatal diagnosis.

Chromosomal aberrations identified in culture of squamous carcinomas are confirmed by fluorescence in situ hybridisation.

R. Zarbo, T. Carey, M. Benninger, 1999, Molecular pathology : MP.

Characterization of human laryngeal primary and metastatic squamous cell carcinoma cell lines UM-SCC-17A and UM-SCC-17B.

D. Schwartz, T. Carey, C. Bradford, 1989, Cancer research.

WHEN ARE ANEUPLOID CELLS CLINICALLY SIGNIFICANT?

Golder N Wilson, L. Weiss, G. Nowinski, 1984, Pediatric Research.

Brief Clinical Report : Duplication 3 p 21-3 pter and Cyclopia

L. Weiss, D. Dyke, D. N. Kurtzman, 2005 .

Common clonal origin of synchronous primary head and neck squamous cell carcinomas: analysis by tumor karyotypes and fluorescence in situ hybridization.

R. Zarbo, T. Carey, M. Benninger, 1995, Human pathology.

Thyroid abnormalities in 20 children with Turner syndrome.

L. Weiss, C. Wolf, D. V. Van Dyke, 1977, The Journal of pediatrics.

Loss of 18q and homozygosity for the DCC locus: possible markers for clinically aggressive squamous cell carcinoma.

C. James, T. Carey, Megan Conlon, 1996, Anticancer Research.

Frequent loss of heterozygosity on chromosome arm 18q in squamous cell carcinomas. Identification of 2 regions of loss--18q11.1-q12.3 and 18q21.1-q23.

T. Carey, C. Bradford, G. Wolf, 1997, Archives of otolaryngology--head & neck surgery.

Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.

P. Ray, L. Weiss, R. Worton, 1990, Journal of medical genetics.

Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation.

S. Schwartz, H. Willard, D. V. Van Dyke, 1996, American journal of human genetics.

The human inactivated X chromosome folds in early metaphase, prometaphase, and prophase

L. Weiss, M. Worsham, D. Dyke, 1987, Human Genetics.

The impact of maternal serum screening programs for Down syndrome in southeast Michigan, 1988–2003

S. Ebrahim, A. Wiktor, M. Micale, 2007, Prenatal diagnosis.

Tumor behavior in transitional cell carcinoma of the bladder in relation to chromosomal markers and histopathology.

B. Miles, L. Weiss, D. V. Van Dyke, 1987, Cancer research.

Multiple active X chromosomes in myelofibrosis with myeloid metaplasia.

L. Weiss, D. V. Van Dyke, D. Dyke, 1981, Cancer genetics and cytogenetics.

Prenatal diagnosis of fetal cystic hygromas associated with generalized lymphangiectasis.

D. V. Van Dyke, B. Madrazo, D. Dyke, 1981, Henry Ford Hospital medical journal.

A dicentric recombinant 9 derived from a paracentric inversion: phenotype, cytogenetics, and molecular analysis of centromeres.

D. Miller, L. Weiss, D. V. Van Dyke, 1989, American journal of human genetics.