H. Wyandt

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Mechanisms of giemsa banding of chromosomes. I. Giemsa-11 banding with azure and eosin.

F. Hecht, H. Wyandt, D. Wysham, 1976, Experimental cell research.

Constitutional partial 1q trisomy mosaicism and Wilms tumor.

J. Milunsky, H. Wyandt, H. Mark, 2005, Cancer genetics and cytogenetics.

A possible exception to the critical region hypothesis.

H. Wyandt, V. Barnabei, T. Kelly, 1981, American journal of human genetics.

Symmetric replication of an unstable isodicentric Xq chromosome derived from isolocal maternal sister chromatid recombination.

J. Milunsky, A. Higgins, R. Lebo, 1999, American journal of medical genetics.

Partial Xq25 deletion in a family with the X-linked lymphoproliferative disease (XLP)

W. Sanger, H. Wyandt, S. Pirruccello, 1990, Cancer Genetics and Cytogenetics.

Localization of the genes for histatins to human chromosome 4q13 and tissue distribution of the mRNAs.

H. Wyandt, F. Oppenheim, A. Milunsky, 1989, American journal of human genetics.

Characterization of a duplication in the terminal band of 4p by molecular cytogenetics.

T. Lerner, J. Gusella, J. Milunsky, 1993, American journal of medical genetics.

Fluorescence in situ hybridization to assess aneuploidy for chromosomes 7 and 8 in hematologic disorders.

M. Salama, H. Wyandt, D. Chinnappan, 1998, Cancer genetics and cytogenetics.

Are balanced translocations really balanced? Preliminary cytogenetic evidence for position effect in man.

F. Hecht, H. Wyandt, B. Kaiser‐Mccaw, 1978, Birth defects original article series.

Ovarian teratomas: cytologic data.

F. Hecht, B. Mccaw, H. Wyandt, 1976, Cytogenetics and cell genetics.

Disease associated balanced chromosome rearrangements (DBCR): report of two new cases.

V. Tonk, D. Morgan, H. Wyandt, 2003, Annales de genetique.

Cytogenetic studies of eight squamous cell carcinomas of the head and neck. Deletion of 7q, a possible primary chromosomal event.

H. Wyandt, A. Milunsky, A. Carlson, 1992, Cancer genetics and cytogenetics.

Chromosomal translocations in secondary acute myeloid leukemia.

J. Rowley, C. Rosenberg, S. Gollin, 1996, The New England journal of medicine.

Gamma heavy chain disease: report of a case associated with trisomy of chromosome 7.

H. Wyandt, C. Hess, D. Innes, 1985, Cancer genetics and cytogenetics.

The mechanism of C- and G-banding of chromosomes.

D. Comings, H. Wyandt, T. Okada, 1973, Experimental cell research.

Evaluation of satellited Y chromosome (Yqs) detected during prenatal diagnosis

B. Haddad, H. Wyandt, A. Milunsky, 1997, Acta obstetricia et gynecologica Scandinavica.

Interstitial deletion involving most of Yq.

H. Wyandt, H. Drwinga, A. Milunsky, 1990, American journal of medical genetics.

A mitotically unstable human dicentric Y chromosome in a male pseudohermaphrodite.

H. Wyandt, A. D'ercole, P. Buchanan, 1976, Cytogenetics and cell genetics.

2 – The Human Cell Nucleus: Quinacrine and Other Differential Stains in the Study of Chromatin and Chromosomes

F. Hecht, R. Magenis, H. Wyandt, 1974 .

Human Y-chromatin. I. Dispersion and condensation.

F. Hecht, H. Wyandt, 1973, Experimental cell research.

Summary of the 1993 ASHG ancillary meeting "recent research on chromosome 4p syndromes and genes".

D. Ledbetter, R. Myers, K. Hirschhorn, 1995, American journal of medical genetics.

Human chromosome 2 rod/ring mosaicism: probable origin by prezygotic breakage and intrachromosomal exchange.

H. Wyandt, A. Lamb, W. Wilson, 1982, Cytogenetics and cell genetics.

A CNV Catalogue

Golder N Wilson, V. Tonk, H. Wyandt, 2017 .

Costovertebral dysplasia in a patient with partial trisomy 22.

V. Tonk, Masamichi Ito, H. Wyandt, 2006, Experimental and molecular pathology.

Cytogenetic and molecular cytogenetic studies of a case of interstitial deletion of proximal 15q

V. Tonk, B. Wu, B. Haddad, 1995, Clinical genetics.

Schizophrenia susceptibility gene locus at Xp22.3

J. Milunsky, H. Wyandt, A. Milunsky, 1999, Clinical genetics.

Tandem duplication/deletion in a maternally derived chromosome 9 supernumerary derivative resulting in 9p trisomy and partial 9q tetrasomy.

J. Milunsky, R. Lebo, H. Wyandt, 2000, American journal of medical genetics.

Partial duplication of Xp: a case report and review of previously reported cases.

H. Wyandt, A. Milunsky, J. Skare, 1991, American journal of medical genetics.

Chromosome deletion of Xq25 in an individual with X-linked lymphoproliferative disease.

W. Sanger, H. Wyandt, D. Purtilo, 1989, American journal of medical genetics.

Heteromorphisms in Clinical Populations

S. Patil, H. Wyandt, 2004 .

Discrepant cytogenetic and fluorescence in situ hybridization results in a 26-year-old male with early T-cell acute lymphocytic leukemia.

K. Miller, H. Wyandt, D. Chinnappan, 1998, Cancer genetics and cytogenetics.

Array-Comparative Genomic Hybridization/Microarray Analysis: Interpretation of Copy Number Variants

Golder N Wilson, V. Tonk, H. Wyandt, 2017 .

Copy Number Variants

V. Tonk, H. Wyandt, 2011 .

Localization of the gene for human heart fatty acid binding protein to chromosome 1p32-1p33

Bai-Lin Wu, H. Wyandt, G. Offner, 1993, Human Genetics.

De novo 21q interstitial deletion in a retarded boy with ulno-fibular dysostosis.

H. Wyandt, J. F. Reynolds, T. Kelly, 1985, American journal of medical genetics.

Report of a variant t(1;15;17)(p36;q22;q21.1) in a patient with acute promyelocytic leukemia.

H. Wyandt, E. Vosburgh, A. Milunsky, 1991, Cancer genetics and cytogenetics.

Interstitial deletion of 8q. Occurrence in a patient with multiple exostoses and unusual facies.

H. Wyandt, W. Wilson, H. Shah, 1983, American journal of diseases of children.

Exclusion gene mapping utilizing patients with chromosome imbalance: The HL-A system as a prototype

F. Hecht, R. Magenis, H. Wyandt, 1975, Humangenetik.

X;Y translocation in a female with streak gonads, H-Y- phenotype, and some features of Turner's syndrome.

S. Wachtel, H. Wyandt, V. Barnabei, 1985, Cytogenetics and cell genetics.

Trisomy 12 mosaicism in phenotypically normal fetuses following prenatal detection

S. Patil, F. Luthardt, H. Wyandt, 1990, Prenatal diagnosis.

Trisomy 15 mosaicism and uniparental disomy (UPD) in a liveborn infant.

J. Milunsky, H. Wyandt, A. Milunsky, 1994, American journal of medical genetics.

Chromosome Heteromorphism (Summaries)

Golder N Wilson, V. Tonk, H. Wyandt, 2017 .

Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH.

J. Milunsky, H. Wyandt, S. Shim, 2006, Experimental and molecular pathology.

Distal 15q trisomy: phenotypic comparison of nine cases in an extended family.

H. Wyandt, M. Robinow, T. Kelly, 1984, American journal of human genetics.

Emerging phenotype of duplication (7p): a report of three cases and review of the literature.

J. Milunsky, H. Wyandt, A. Milunsky, 1989, American journal of medical genetics.

Redacted for Privacy

H. Wyandt, 2011 .

Colored reverse-banding of human chromosomes with acridine orange following alkaline/formalin treatment: Densitometric validation and applications

F. Hecht, R. Vlietinck, R. Magenis, 1974, Humangenetik.

Reciprocal translocation 14q;21q in a patient with the Brachmann-de Lange syndrome.

H. Wyandt, W. Wilson, J. Kennaugh, 1983, Journal of medical genetics.

Gene and Genome Sequencing: Interpreting Genetic Variation at the Nucleotide Level

Golder N Wilson, V. Tonk, H. Wyandt, 2017 .

Potentiality of the murine colony-forming cells detected by an in vivo diffusion chamber culture system.

H. Wyandt, E. Niskanen, 1985, Blood.

Deletion of 15q12 in Angelman syndrome: report of 3 new cases

V. Tonk, H. Wyandt, A. Milunsky, 1992, Clinical genetics.

Unusual dental findings in a patient with a rare bone dysplasia (dyschondrosteosis) and a chromosomal anomaly.

H. Wyandt, R. Stewart, E. Lovrien, 1971, Oral surgery, oral medicine, and oral pathology.

Study of a patient with apparent monosomy 21 owing to translocation: 45,XX,21-,t(18q+).

F. Hecht, H. Wyandt, R. Stewart, 1971, Cytogenetics.

Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22p24).

A. Lin, B. Haddad, H. Wyandt, 1996, Journal of medical genetics.

Mosaicism with translocation: autoradiographic and fluorescent studies of an inherited reciprocal translocation t(2q+;14q-).

F. Hecht, J. Reiss, R. Magenis, 1972, Journal of medical genetics.

Prenatal diagnosis using interphase fluorescence in situ hybridization (FISH): 2‐year multi‐center retrospective study and review of the literature

P. N. Rao, M. Schoonmaker, H. Wyandt, 2001, Prenatal diagnosis.

Parental origin of a ring 13 chromosome in a female with multiple anomalies

R. Magenis, H. Wyandt, K. Overton, 1976, Human Genetics.

Reported tandem duplication/deletion of 9q is actually an inverted duplication.

H. Wyandt, 2001, American journal of medical genetics.

Chromosome Variation Detected by Fluorescent In Situ Hybridization (FISH)

Golder N Wilson, V. Tonk, H. Wyandt, 2017 .

7 FISH Technologies

V. Tonk, H. Wyandt, 2004 .

9p trisomy identified by Giemsa-11

F. Hecht, R. Magenis, H. Wyandt, 1976, Human Genetics.

Atlas of Human Chromosome Heteromorphisms

V. Tonk, H. Wyandt, 2004, Springer Netherlands.

Brachmann-de Lange syndrome . in a patient with the Reciprocal translocation 14 q ; 21 q

H. Wyandt, W. Wilson, J. Kennaugh, 2022 .

Human Chromosome Variation: Heteromorphism and Polymorphism

V. Tonk, H. Wyandt, 2011, Springer Netherlands.

Giemsa-11 staining of chromosome 1: a newly described heteromorphism.

T. Donlon, H. Wyandt, R. E. Maegenis, 1978, Science.

Normal Population Studies

V. Tonk, H. Wyandt, 2004 .

Secondary amenorrhoea and 47,XX,i(Xq) karyotype.

H. Wyandt, J. Wilks, T. Kelly, 1986, Journal of medical genetics.

Interstitial 3p deletion in a child due to paternal paracentric inserted inversion.

H. Wyandt, T. Kelly, R. Kasprzak, 1980, American journal of human genetics.

Familial partial 14 trisomy.

T. McConnell, H. Wyandt, J. Miller, 1979, Journal of medical genetics.

Transmission of ring 14 chromosome from mother to two sons.

R. Matalon, H. Wyandt, I. Rosenthal, 1990, American journal of medical genetics.

Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G‐banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high‐resolution comparative genomic hybridization

H. Wyandt, J. Milunsky, X‐L Huang, 2005, Clinical genetics.

Restrictive consent and amniocentesis.

H. Wyandt, G. Prescott, P. Garlinger, 1973, The New England journal of medicine.

X;Y translocation in a female with streak gonads, H-Y– phenotype, and some features of Turner’s syndrome

S. Wachtel, H. Wyandt, V. Barnabei, 1984 .

Correlation of Abnormal Rapid FISH and Chromosome Results from Amniocytes for Prenatal Diagnosis

J. Milunsky, V. Tonk, H. Wyandt, 2006, Fetal Diagnosis and Therapy.

46,XY/47,XYY male with the fragile X syndrome: cytogenetic and molecular studies.

J. Herskowitz, L. Farrer, H. Wyandt, 1993, American journal of medical genetics.

Trisomy 18/trisomy 13 mosaicism in an adult with profound mental retardation and multiple malformations.

H. Wyandt, M. Shires, W. Wilson, 1983, American journal of medical genetics.

Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis

Golder N Wilson, V. Tonk, H. Wyandt, 2017 .

In situ hybridization applied to Waardenburg syndrome.

C. Baldwin, B. Wu, H. Wyandt, 1993, Cytogenetics and Cell Genetics.

Detection of the X-chromatin body in human fibroblasts by quinacrine fluoromicroscopy.

F. Hecht, H. Wyandt, 1971, Lancet.

Quinacrine studies of sex chromatin and nucleoli in human Brain

H. Wyandt, R. Iorio, 1973, Humangenetik.

Association of a chromatin mass with the fluorescent Y-body in human interphase nuclei.

F. Hecht, H. Wyandt, 1972, Experimental cell research.

Familial supernumerary chromosome and malignancy.

J. Milunsky, H. Wyandt, A. Milunsky, 1996, Cancer genetics and cytogenetics.

Recurrent proximal 18p monosomy and 18q trisomy in a family with a maternal pericentric inversion of chromosome 18.

H. Wyandt, K. Prabhakara, A. R. Ramadevi, 2004, Annales de genetique.

Chromosome 21

H. Wyandt, Vijay S. Tonk, 2020, Definitions.

Chromosome 19

H. Wyandt, H. Ohashi, Vijay S. Tonk, 2020, Definitions.

Human Y-chromatin: III. The nucleolus

H. Wyandt, R. Iorio, 1973 .

Chromosomal Localization of the Heterochromatic Region 16qh(.76) linked to α-Haptoglobin in Man

F. Hecht, W. Kimberling, R. Magenis, 1971, Nature.

Mechanisms of Giemsa banding

F. Hecht, H. Wyandt, S. Patil, 1980, Human Genetics.

Modification of CMT1 Phenotypes by the Independent Coexisting Neurogenetic Disorders, McArdle Disease and Chromosome 5p Trisomy

R. Lebo, H. Wyandt, A. Hahn, 1999, Annals of the New York Academy of Sciences.

Tandem duplication/deletion in a maternally derived chromosome 9 supernumerary derivative resulting in 9p trisomy and partial 9q tetrasomy.

J. Milunsky, R. Lebo, H. Wyandt, 2000, American journal of medical genetics.

Chromosome 22

H. Wyandt, Vijay S. Tonk, 2020, Definitions.

Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22p24).

A. Lin, B. Haddad, H. Wyandt, 1996, Journal of medical genetics.