S. Jalal

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Familial 22q11.2 deletions in DiGeorge/velocardiofacial syndrome are predominantly smaller than the commonly observed 3Mb

R. Ketterling, H. Flynn, A. Adeyinka, 2004, Genetics in Medicine.

Inherited interstitial deletion of chromosomes 5p and 16q without apparent phenotypic effect: further confirmation

J. Hand, R. Ketterling, V. Michels, 2000, Prenatal diagnosis.

Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies.

N. Ammash, V. Michels, C. Warnes, 2005, Journal of the American College of Cardiology.

Coexistence of aneuploid subclones within a myeloma cell line that exhibits clonal immunoglobulin gene rearrangement: clinical implications.

G. Ahmann, J. Katzmann, R. Kyle, 1993, Cancer research.

Application of fluorescent in situ hybridization with X and Y chromosome specific probes to buccal smear analysis.

A. Zinsmeister, G. Dewald, R. Jenkins, 1996, American journal of medical genetics.

Highly sensitive fluorescence in situ hybridization method to detect double BCR/ABL fusion and monitor response to therapy in chronic myeloid leukemia.

A. Zinsmeister, R. Silver, G. Dewald, 1998, Blood.

Two rare cases of 6p partial deletion

S. Jalal, V. Macias, H. Roop, 1989, Clinical genetics.

Detection of t(2;5) in anaplastic large cell lymphoma: comparison of immunohistochemical studies, FISH, and RT-PCR in paraffin-embedded tissue.

S. Ansell, K. Pulford, D. Arber, 1999, The American journal of surgical pathology.

DDT induced chromosome mutations in mice--further testing.

S. Jalal, K. D. Larsen, 1974, Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie.

Clinical significance of the translocation (11;14)(q13;q32) in multiple myeloma.

G. Ahmann, R. Fonseca, A. Dispenzieri, 1999, Leukemia & lymphoma.

Multiple myeloma and the translocation t(11;14)(q13;q32): a report on 13 cases

R. Fonseca, R. Kyle, M. Gertz, 1998, British journal of haematology.

Prognostic factors for hyperdiploid-myeloma: effects of chromosome 13 deletions and IgH translocations

G. Ahmann, P. L. Bergsagel, R. Fonseca, 2006, Leukemia.

A novel three-color, clone-specific fluorescence in situ hybridization procedure for monoclonal gammopathies.

G. Ahmann, P. Greipp, G. Dewald, 1998, Cancer genetics and cytogenetics.

Characteristics of two cases with dup(15) (q 11.2-q 12): one of maternal and one of paternal origin

D. Babovic‐Vuksanovic, K. Snow, V. Michels, 2000, Genetics in Medicine.

De novo 16p deletion: ATR-16 syndrome.

S. Thibodeau, N. Lindor, M. Wick, 1997, American journal of medical genetics.

Use of fluorescent in situ hybridization for marker chromosome identification in congenital and neoplastic disorders.

M. Tallman, R. Jenkins, L. P. Cook, 1991, American journal of clinical pathology.

Efficacy of fluorescence in situ hybridization for detecting PML/RARA gene fusion in treated and untreated acute promyelocytic leukemia.

G. Dewald, E. Paietta, C. Hanson, 1994, Mayo Clinic proceedings.

6q deletion in Waldenström macroglobulinemia is associated with features of adverse prognosis

J. Hernández-Rivas, R. Fonseca, A. Dispenzieri, 2007, British journal of haematology.

Fluorescence in situ hybridization with X and Y chromosome probes for cytogenetic studies on bone marrow cells after opposite sex transplantation.

A. Zinsmeister, G. Dewald, R. Jenkins, 1993, Bone marrow transplantation.

Multiple primary tumors associated with chromosome 9p deletion

N. Lindor, Seema Kumar, A. Lteif, 2007, American journal of medical genetics. Part A.

Spectral karyotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalities

L. Shaffer, P. O’Brien, E. Schröck, 1997, Human Genetics.

Subtelomere deletions and translocations are frequently familial

D. V. Van Dyke, A. Adeyinka, C. P. Lorentz, 2005, American journal of medical genetics. Part A.

Utility of subtelomeric fluorescent DNA probes for detection of chromosome anomalies in 425 patients

D. Babovic‐Vuksanovic, R. Ketterling, V. Michels, 2003, Genetics in Medicine.

Molecular cytogenetic characterization of a de novo unbalanced translocation leading to trisomy 17q25→qter and monosomy 18p11.3→pter in a girl with dysmorphic features

R. Michaelis, G. Velagaleti, T. Rowe, 2003, Clinical dysmorphology.

Chromosomal abnormalities in systemic amyloidosis

T. Therneau, G. Ahmann, R. Fonseca, 1998, British journal of haematology.

Molecular Diagnosis of Ewing's Sarcoma/Primitive Neuroectodermal Tumor in Formalin-Fixed Paraffin-Embedded Tissues by RT-PCR and Fluorescence In Situ Hybridization

X. Qian, R. Lloyd, R. Ketterling, 2005, Diagnostic molecular pathology : the American journal of surgical pathology, part B.

Analysis of Hurthle Cell Neoplasms of the Thyroid by Interphase Fluorescence In Situ Hybridization

R. Lloyd, P. Roche, J. Goellner, 2001, The American journal of surgical pathology.

Genotoxicity of the organophosphorus insecticide chlorpyrifos based on human lymphocyte culture.

O. R. Larson, S. Jalal, M. C. Nelson, 1990 .

DNA fluorescent probes for diagnosis of velocardiofacial and related syndromes.

D. Driscoll, G. Dewald, V. Michels, 1995, Mayo Clinic proceedings.

FISH Demonstrates Treatment-Related Chromosome Damage in Myeloid but not Plasma Cells in Primary Systemic Amyloidosis

G. Ahmann, R. Fonseca, R. Kyle, 2000, Leukemia and Lymphoma.

Induced clastogenicity in white rats by the herbicide 2,4-D.

S. Jalal, T. Turkula, 1987 .

DDT-induced chromosomal damage in mice.

G. A. Johnson, S. Jalal, 1973, The Journal of heredity.

Cytological differentiation of constitutive heterochromatin

T. Hsu, S. Pathak, S. Jalal, 2004, Chromosoma.

Meiotic Behavior and Fertility Interrelationship in Andropogon scoparius and A. gerardi

G. Dewald, S. Jalal, 1974 .

Chromosomal Aberrations and Fertility Interrelationships in Prairie Bromus inermis Leyss. Populations

S. Jalal, T. Lafleur, 1972 .

Dynamics of chromosome spreading.

A R Zinsmeister, A. Zinsmeister, J. Spurbeck, 1996, American journal of medical genetics.

Subdivision of the human Y chromosome

T. Hsu, S. Pathak, R. Pfeiffer, 2004, Humangenetik.

Position effects due to chromosome breakpoints that map ∼900 Kb upstream and ∼1.3 Mb downstream of SOX9 in two patients with campomelic dysplasia

P. Stankiewicz, J. Lupski, M. Withers, 2005 .

Position effects due to chromosome breakpoints that map approximately 900 Kb upstream and approximately 1.3 Mb downstream of SOX9 in two patients with campomelic dysplasia.

P. Stankiewicz, J. Lupski, M. Withers, 2005, American journal of human genetics.

Familial interstitial deletion of chromosome 4 (p15.2p16.1).

V. Tonk, G. Velagaleti, S. Jalal, 2003, Annales de genetique.

Rothmund-Thomson syndrome due to RECQ4 helicase mutations: report and clinical and molecular comparisons with Bloom syndrome and Werner syndrome.

N. Lindor, A. Shimamoto, Y. Furuichi, 2000, American journal of medical genetics.

Rothmund‐Thomson syndrome in siblings: evidence for acquired in vivo mosaicism

S. Thibodeau, L. Kvols, N. Lindor, 1996, Clinical genetics.

Search for chromosome instability in lymphocytes with germ-line mutations in DNA mismatch repair genes.

S. Thibodeau, J. Cunningham, N. Lindor, 1998, Cancer genetics and cytogenetics.

Partial trisomy 7p associated with familial 7p;22q translocation.

L. Larson, S. Jalal, W. Wasdahl, 1977, Journal of medical genetics.

FISH—Clinical Applications of 24‐Color FISH

A. Adeyinka, S. Jalal, 2004 .

Method for sequential staining of GTL-banded metaphases with fluorescent-labeled chromosome-specific paint probes.

G. Dewald, M. Law, E. Christensen, 1993, American journal of medical genetics.

Familial Adenomatous Polyposis and Mental Retardation Caused by a de novo Chromosomal Deletion at 5q15-q22: Report of a Case

K. Offit, S. Jhanwar, J. Guillem, 2005, Diseases of the colon and rectum.

Reflex fluorescent in situ hybridization testing for unsuccessful product of conception cultures: A retrospective analysis of 5555 samples attempted by conventional cytogenetics and fluorescent in situ hybridization

E. Thorland, R. Ketterling, S. Jalal, 2011, Genetics in Medicine.

Complete trisomy 17p a relatively new syndrome.

L. Larson, S. Jalal, M. Kukolich, 1988, Annales de genetique.

Duplication 6q24 6qter in an infant from a balanced paternal translocation

J. Opitz, T. Chase, S. Jalal, 1983 .

Cytogenetic and clinical characteristics of a case involving complete duplication of Xpter-->Xq13.

N. Lindor, R. Dahl, D. Zimmerman, 1996, Journal of medical genetics.

Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients.

E. Thorland, N. Lindor, D. Dawson, 2003, American journal of human genetics.

Autism, profound mental retardation and atypical bipolar disorder in a 33-year-old female with a deletion of 15q12.

L. Burd, J. Kerbeshian, S. Jalal, 2008, Journal of mental deficiency research.

Form of 15q proximal duplication appears to be a normal euchromatic variant.

N. Lindor, G. Dewald, D. Persons, 1994, American journal of medical genetics.

early genetic events in patients with primary systemic amyloidosis Translocations involving the immunoglobulin heavy-chain locus are possible

G. Ahmann, R. Fonseca, A. Dispenzieri, 2011 .

Translocations involving the immunoglobulin heavy-chain locus are possible early genetic events in patients with primary systemic amyloidosis.

G. Ahmann, R. Fonseca, A. Dispenzieri, 2001, Blood.

Uniparental disomy in congenital disorders: a prospective study.

S. Thibodeau, N. Lindor, G. Dewald, 1995, American journal of medical genetics.

Trisomy 20 mosaicism caused by a maternal meiosis II error is associated with normal intellect but multiple congenital anomalies

J. Ellison, D. Dawson, S. Jalal, 2005, American journal of medical genetics. Part A.

The application of fluorescent in situ hybridization to detect Mbcr/abl fusion in variant Ph chromosomes in CML and ALL.

A R Zinsmeister, S N Thibodeau, A. Zinsmeister, 1993, Cancer genetics and cytogenetics.

Trisomy 18 syndrome with an unusual karyotype: possible double isochromosome.

L. Larson, J. Saumur, S. Jalal, 1978, Journal of medical genetics.

Trisomy 22: no longer an enigma.

S. Jalal, M. Kukolich, A. Kulharya, 1989, American journal of medical genetics.

Analysis of Parathyroid Neoplasms by Interphase Fluorescence In Situ Hybridization

R. Lloyd, L. Erickson, Long Jin, 2004, The American journal of surgical pathology.

heavy chain locus translocations but have frequent 6q deletions Waldenström macroglobulinemia neoplastic cells lack immunoglobulin

G. Ahmann, R. Fonseca, R. Kyle, 2013 .

Waldenström macroglobulinemia neoplastic cells lack immunoglobulin heavy chain locus translocations but have frequent 6q deletions.

G. Ahmann, R. Fonseca, R. Kyle, 2002, Blood.

Clinical characteristics associated with dup17(q24q25.1) in a mosaic mother and two non-mosaic daughters.

N. Lindor, D. Babovic‐Vuksanovic, J. Westman, 1998, Clinical Dysmorphology.

Subtelomeric deletion of 18p in an adult with paranoid schizophrenia and mental retardation

D. Babovic‐Vuksanovic, S. Jenkins, R. Ensenauer, 2004, American journal of medical genetics. Part A.

Trisomy 21 as the only recurrent chromosomal anomaly in a clinically aggressive ovarian carcinoma.

S. Faruqi, S. Jalal, R. Deger, 2002, Cancer genetics and cytogenetics.

Voltage-gated calcium channel γ2 subunit gene is not deleted in velo-cardio-facial syndrome

L. Krahn, J. Black, S. Jalal, 2001, Molecular Psychiatry.

Duplication 6q24 leads to 6qter in an infant from a balanced paternal translocation.

T. Chase, S. Jalal, J. Martsolf, 1983, American journal of medical genetics.

Nonmosaic smallest duplication of 12q24.31‐qter: The first reported case

N. Lindor, S. Jalal, Pamela S. McGrann, 2004, American journal of medical genetics. Part A.

Partial 6p trisomy associated with infantile autism

L. Burd, J. Kerbeshian, S. Jalal, 1988, Clinical genetics.

Unbalanced cryptic 5p deletion/17p duplication identified by subtelomeric FISH in a family with a boy with chimerism and a balanced t(4;5)

D. Babovic‐Vuksanovic, R. Ensenauer, S. Jalal, 2004, American journal of medical genetics. Part A.

Visual impairment due to macular disciform scars in a 20-year-old man with Smith-Magenis syndrome: another ophthalmologic complication.

N. Lindor, D. Babovic‐Vuksanovic, D. Robertson, 1998, American journal of medical genetics.

Mosaic ring 20 with no detectable deletion by FISH analysis: Characteristic seizure disorder and literature review

E. Thorland, V. Michels, D. V. Van Dyke, 2006, American journal of medical genetics. Part A.

Familial transmission of Wolf syndrome resulting from specific deletion 4p16 from t(4;8)(p16;p21) mat.

T. Chase, S. Jalal, J. Martsolf, 1987, Clinical genetics.

Delineation of the cryptic 1qter deletion phenotype

J. Merritt, V. Michels, S. Jalal, 2007, American journal of medical genetics. Part A.

Human SULT1A3 pharmacogenetics: gene duplication and functional genomic studies.

R. Weinshilboum, E. Wieben, Y. Martin, 2004, Biochemical and biophysical research communications.

Cytogenetic guidelines for fragile X studies tested in routine practice.

G. Dewald, J. Spurbeck, S. Jalal, 1992, American journal of medical genetics.

Detection of diagnostically critical, often hidden, anomalies in complex karyotypes of haematological disorders using multicolour fluorescence in situ hybridization

R. Fonseca, M. Law, C. Hanson, 2001, British journal of haematology.

Euchromatic 16p+ heteromorphism: first report in North America.

Golder N Wilson, N. Schneider, G. Wilson, 1990, American journal of medical genetics.

Cytogenetic testing for Williams syndrome.

V. Michels, P. Karnes, S. Jalal, 1996, Mayo Clinic proceedings.

Frequency and photographs of HGM11 chromosome anomalies in bone marrow samples from 3,996 patients with malignant hematologic neoplasms.

G. Dewald, S. Jalal, C. R. Schad, 1993, Cancer genetics and cytogenetics.

Deletions of 17p13.1 and 13q14 are uncommon in Waldenström macroglobulinemia clonal cells and mostly seen at the time of disease progression.

Robert A Kyle, Rafael Fonseca, G. Ahmann, 2002, Cancer genetics and cytogenetics.

A validated FISH trisomy index demonstrates the hyperdiploid and nonhyperdiploid dichotomy in MGUS.

G. Ahmann, P. L. Bergsagel, R. Fonseca, 2005, Blood.

Ploidy status rarely changes in myeloma patients at disease progression.

G. Ahmann, P. L. Bergsagel, R. Fonseca, 2006, Leukemia research.

nonhyperdiploid dichotomy in MGUS A validated FISH trisomy index demonstrates the hyperdiploid and

G. Ahmann, R. Fonseca, M. Oken, 2013 .

Inverted duplication involving alpha satellite DNA resulting in a C-negative-band in the qh region of chromosome 16.

G. Dewald, M. Law, S. Jalal, 1993, American journal of medical genetics.

Euchromatic 9q + heteromorphism in a family.

S. Jalal, M. Kukolich, D. Day, 1990, American journal of medical genetics.

Genetic testing for Prader-Willi and Angelman syndromes.

S. Thibodeau, S. Jalal, C. Schad, 1995, Mayo Clinic proceedings.

Mosaic r(13) resulting in large deletion of chromosome 13q in a newborn female with multiple congenital anomalies.

D. Babovic‐Vuksanovic, D. Thompson, C. P. Lorentz, 2002, American journal of medical genetics.

Rare 15q duplication in an abortus.

S. Jalal, D. Day, M. Nelson, 1989, American journal of medical genetics.

Demonstration of Robertsonian fusion by silver staining in a 13/14 translocation in man.

S. Jalal, M. Coleman, W. A. Washahl, 1982, Cytologia.

Ring chromosome 8 syndrome: further characterization.

V. Tonk, D. Morgan, S. Jalal, 2000, American journal of medical genetics.

Tandem translocation of chromosomes 22 and 15 with two preserved satellite stalk regions and deletion 22q13.3-qter.

M. Law, S. Jalal, M. H. Lee, 2001, American journal of medical genetics.

Cryptic duplication of 12q24.33 → qter in a child with Angelman syndrome—simultaneous occurrence of two unrelated cytogenetic events

U. Surti, J. Vockley, J. Bedoyan, 2007, American journal of medical genetics. Part A.

Unique case of mosaicism involving two morphologically similar marker chromosomes of different centric origin in a patient with developmental delay.

K. Hirschhorn, V. Tonk, P. Warburton, 2002, American journal of medical genetics.

Genotoxicity of the Organophosphorus Insecticide Malathion based on Human Lymphocytes in Culture

J. Herath, M. Ebertz, S. Jalal, 1989 .

2,4-D induced clastogenicity and elevated rates of sister chromatid exchanges in cultured human lymphocytes.

C. Korte, S. Jalal, 1982, The Journal of heredity.

Further characterization of human fetal osteoblastic hFOB 1.19 and hFOB/ERα cells: Bone formation in vivo and karyotype analysis using multicolor fluorescent in situ hybridization

M. Subramaniam, T. Spelsberg, M. Bolander, 2002, Journal of cellular biochemistry.

14q32.3 deletion syndrome with autism

D. Babovic‐Vuksanovic, J. Merritt, S. Jalal, 2005, American journal of medical genetics. Part A.

Severe suppression of Frzb/sFRP3 transcription in osteogenic sarcoma.

M. Yaszemski, Deendayal Mandal, F. Bertoni, 2007, Gene.

Utility of multicolor fluorescent in situ hybridization in clinical cytogenetics

M. Law, Syed M Jalal, Mark E Law, 1999, Genetics in Medicine.

Direct chromosome analysis from neonatal cord blood.

S. Jalal, M. Kukolich, D. Day, 1988, American journal of medical genetics.

Detection of newborn aneuploidy by interphase fluorescence in situ hybridization.

M. Law, S. Jalal, 1997, Mayo Clinic proceedings.

Prenatal detection of aneuploidy by directly labeled multicolored probes and interphase fluorescence in situ hybridization.

G. Dewald, M. Law, S. Jalal, 1998, Mayo Clinic proceedings.

Guidelines for buccal smear collection in breast-fed infants.

N. Lindor, D. Babovic‐Vuksanovic, R. Bailey, 1999, American journal of medical genetics.

Maternal cell contamination of buccal smear samples in nursing neonates

N. Lindor, D. Babovic‐Vuksanovic, V. Michels, 1998, Clinical Genetics.

Differential chromosomal fluorescence with 33258 Hoechst.

T. Hsu, S. Jalal, A. Markvong, 1975, Experimental cell research.

Partial 18 trisomy (with 47 chromosomes) resulting from a familial maternal translocation.

S. Jalal, K. Fried, G. Mundel, 1978, Journal of medical genetics.

Tissue, cell type, and breast cancer stage‐specific expression of a TGF‐β inducible early transcription factor gene

B. Riggs, B. L. Riggs, T. Hefferan, 1998, Journal of cellular biochemistry.

Application of multicolor fluorescent in situ hybridization for enhanced characterization of chromosomal abnormalities in congenital disorders.

N. Lindor, M. Law, G. Sekhon, 2001, Mayo Clinic proceedings.

Pulmonary lymphangioleiomyomatosis in a man.

M. Aubry, E. Henske, J. Myers, 2000, American journal of respiratory and critical care medicine.

Increased rates of sister chromatid exchanges induced by the herbicide 2,4-D.

S. Jalal, T. Turkula, 1985, The Journal of heredity.