G. Stetten

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Partial trisomies in two spontaneously arising long-lived human keratinocyte lines

J. Weaver, G. Stetten, J. Littlefield, 1991, In Vitro Cellular & Developmental Biology - Animal.

G. Stetten, S. Lederberg, 1973, The Journal of cell biology.

Molecular genetic approach to the characterization of the "Down syndrome region" of chromosome 21.

D. J. Driscoll, S. Antonarakis, G. Stetten, 1989, Genomics.

A cre-lox recombination system for the targeted integration of circular yeast artificial chromosomes into embryonic stem cells.

J. Gearhart, G. Stetten, L. Call, 2000, Human molecular genetics.

Special Notice to Contributors

S. Ennis, C. Auffray, W. Linehan, 1996 .

Visualization of centromere proteins CENP-B and CENP-C on a stable dicentric chromosome in cytological spreads

W. Earnshaw, G. Stetten, H. Ratrie, 1989, Chromosoma.

Amniotic fluid steroid levels. Fetuses with adrenal hyperplasia, 46,XXY fetuses, and normal fetuses.

P. A. Lee, G. Stetten, C. Migeon, 1982, American journal of diseases of children.

Use of T-Cell Antibodies for Donor Dosaging in a Canine Model of in utero Hematopoietic Stem Cell Transplantation

M. Torbenson, K. Murphy, Richard J. Jones, 2007, Fetal Diagnosis and Therapy.

In utero hematopoietic stem cell transplantation with haploidentical donor adult bone marrow in a canine model.

S. South, K. Murphy, Richard J. Jones, 2004, American journal of obstetrics and gynecology.

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.

Genomic structure of PEX13, a candidate peroxisome biogenesis disorder gene.

D. Crane, S. Gould, G. Stetten, 1998, Genomics.

Multiple Tissues in a Mouse Model of Down Syndrome Transcript Level Alterations Reflect Gene Dosage Effects Across

S. South, H. Lehrach, M. Sultan, 2006 .

Translocation of the nucleolus organizer region to the human X chromosome.

B. Migeon, J. Axelman, G. Stetten, 1986, American journal of human genetics.

INCIDENCE AND SIGNIFICANCE OF CHROMOSOME MOSAICISM INVOLVING AN AUTOSOMAL STRUCTURAL ABNORMALITY DIAGNOSED PRENATALLY THROUGH AMNIOCENTESIS: A COLLABORATIVE STUDY

B. Crandall, G. Stetten, J. Priest, 1996, Prenatal diagnosis.

Prenatal diagnosis using DNA polymorphisms. Report on 95 pregnancies at risk for sickle-cell disease or beta-thalassemia.

S. Antonarakis, H. Kazazian, C. Boehm, 1983, The New England journal of medicine.

Recent developments in the detection of deoxyribonucleic acid synthesis by 33258 Hoechst fluorescence.

H. Willard, S. Latt, G. Stetten, 1975, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Prenatal Detection of an Interstitial Deletion in 4p15 in a Fetus with an Increased Nuchal Skin Fold Measurement

S. South, K. Blakemore, G. Stetten, 2004, Fetal Diagnosis and Therapy.

In utero Hematopoietic Stem Cell Transplantation in Canines: Exploring the Gestational Age Window of Opportunity to Maximize Engraftment

M. Torbenson, K. Murphy, Richard J. Jones, 2013, Fetal Diagnosis and Therapy.

Cloning and characterization of a secreted frizzled-related protein that is expressed by the retinal pigment epithelium.

P. Campochiaro, D. Zack, J. Chang, 1999, Human molecular genetics.

Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panel

J. Korenberg, Shibo Li, G. Stetten, 2001, Genetics in medicine : official journal of the American College of Medical Genetics.

Ring Chromosome 21: Characterization of DNA Sequences at Sites of Breakage and Reunion

S. Antonarakis, J. Gusella, H. Kazazian, 1985, Annals of the New York Academy of Sciences.

X-linked adrenoleukodystrophy: ABCD1 de novo mutations and mosaicism.

A. Moser, G. Raymond, C. Reeves, 2011, Molecular genetics and metabolism.

X inactivation in triploidy and trisomy: the search for autosomal transfactors that choose the active X

B. Migeon, P. Jacobs, G. Stetten, 2008, European Journal of Human Genetics.

Reevaluating confined placental mosaicism

S. South, K. Blakemore, G. Stetten, 2004, American journal of medical genetics. Part A.

Mechanisms of ring chromosome formation in 11 cases of human ring chromosome 21.

H. Kazazian, G. Stetten, M. Petersen, 1992, American journal of human genetics.

Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene

Ada Hamosh, Reed E. Pyeritz, E. Puffenberger, 1991, Nature.

Clinical consequences of an increasing trend of preferential use of cultured villi for molecular diagnosis by CVS

C. Boehm, K. Blakemore, G. Stetten, 2008, Prenatal diagnosis.

Revised genomic organization of FBN1 and significance for regulated gene expression.

F. Spencer, H. Dietz, G. Stetten, 1999, Genomics.

Spectral studies on 33258 Hoechst and related bisbenzimidazole dyes useful for fluorescent detection of deoxyribonucleic acid synthesis.

S. Latt, G. Stetten, S A Latt, 1976, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Induction by alkylating agents of sister chromatid exchanges and chromatid breaks in Fanconi's anemia.

S. Latt, G. Stetten, G. Buchanan, 1975, Proceedings of the National Academy of Sciences of the United States of America.

X-Linked Adrenoleukodystrophy: Genes, Mutations, and Phenotypes

J. Pevsner, P. Watkins, L. Braiterman, 2004, Neurochemical Research.

Nonrandom inactivation of the Y-bearing X chromosome in a 46,XX individual: evidence for the etiology of 46,XX true hermaphroditism.

P. Pearson, G. Stetten, C. Migeon, 1994, Cytogenetics and cell genetics.

The role of the sex-determining region Y gene in the etiology of 46,XX maleness.

P. Goodfellow, G. Stetten, C. Migeon, 1993, The Journal of clinical endocrinology and metabolism.

Ambiguous genitalia in an elderly woman with a mosaic 45,X/46,X,dic(Y)(Q11.2) karyotype.

G. Stetten, J. Gearhart, C. Isacson, 1996, Urology.

Molecular mechanism in the formation of a human ring chromosome 21.

S. Antonarakis, W. Earnshaw, G. Stetten, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Region‐specific FISH probes used to identify and characterize an interstitial paracentric inv(21)(q22.1q22.3)

K. Blakemore, G. Stetten, C. Escallon, 1998, Prenatal diagnosis.

Teratologic and mutagenic studies with intrauterine quinacrine hydrochloride.

T. Parmley, G. Stetten, Blake Da, 1983 .

Late prenatal diagnosis of fetal trisomy 18 associated with severe intrauterine growth retardation.

G. Stetten, T. Johnson, V. Corson, 1982, The Johns Hopkins medical journal.

Integration of cytogenetic with recombinational and physical maps of mouse chromosome 16.

B. Birren, R. Reeves, G. Stetten, 1999, Genomics.

The role of the sex-determining region of the Y chromosome (SRY) in the etiology of 46,XX true hermaphroditism

P. Goodfellow, G. Stetten, C. Migeon, 1992, Human Genetics.

Clonal evolution in human lymphoblast cultures.

B. Migeon, J. Axelman, G. Stetten, 1988, American journal of human genetics.

A cystic fibrosis bronchial epithelial cell line: immortalization by adeno-12-SV40 infection.

R. Craig, G. Cutting, G. Cutting, 1991, American journal of respiratory cell and molecular biology.

Origin of chromosome rearrangements in two long-lived human keratinocyte lines

P. Pearson, G. Stetten, J. Littlefield, 1991, In Vitro Cellular & Developmental Biology - Animal.

A complex chromosomal rearrangement detected prenatally and studied by fluorescence in situ hybridization

P. Pearson, D. Batista, G. Stetten, 1993, Human Genetics.

Segregation of a familial balanced (12;10) insertion resulting in Dup(10)(q21.2q22.1) and Del(10)(q21.2q22.1) in first cousins.

G. Semenza, K. Doheny, M. Schwartz, 1997, American journal of medical genetics.

A paternally derived inverted duplication of 7q with evidence of a telomeric deletion.

A. F. Scott, K. Blakemore, G. Stetten, 1997, American journal of medical genetics.

An accessory marker derived from chromosome 20 and its co‐existence with a mosaic trisomy 20 cell line

K. Blakemore, D. Batista, G. Stetten, 1995, Prenatal diagnosis.

Molecular analysis of a complex chromosomal rearrangement and a review of familial cases.

D. Batista, G. Stetten, G. Pai, 1994, American journal of medical genetics.

Unbalanced translocation, t(18;21), detected by fluorescence in situ hybridization (FISH) in a child with 18q- syndrome and a ring chromosome 21.

S. Antonarakis, P. Pearson, G. Stetten, 1993, American journal of medical genetics.

Analysis of reciprocal translocations by chromosome painting: applications and limitations of the technique.

P. Pearson, K. Blakemore, G. Stetten, 1992, American journal of human genetics.

Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of down syndrome.

S. South, H. Lehrach, M. Sultan, 2004, Genome research.

New cytogenetic technology and its application in maternal-fetal medicine

G. Stetten, H. Fox, B. Goodman, 1997 .

Molecular cytogenetic analysis and clinical findings in a newborn with prenatally diagnosed rec(7)dup(7q)inv(7)(p22q31.3)pat

K. Blakemore, G. Stetten, E. Gurewitsch, 1999, Prenatal diagnosis.

Prenatal diagnosis of hemoglobinopathies by restriction endonuclease analysis: pregnancies at risk for sickle cell anemia and S--O Arab disease.

A. F. Scott, H. Kazazian, G. Stetten, 1979, The Johns Hopkins medical journal.

Immunolocalization of CENP-A suggests a distinct nucleosome structure at the inner kinetochore plate of active centromeres

C. Tyler-Smith, D. Warburton, K. Sullivan, 1997, Current Biology.

Trophoblast inclusions are rare in elective terminations and normal deliveries, but common in cases with karyotypic abnormalities

H. Kliman, G. Stetten, X. Ying, 2003 .

Non‐mosaic trisomy 20 presenting at 21 weeks' gestation as a thoraco‐abdominal mass

K. Blakemore, G. Stetten, R. Driggers, 2001, Prenatal diagnosis.

Unusual and rapid amniotic fluid cell growth.

G. Stetten, H. Meißner, 1981, American journal of obstetrics and gynecology.

Autopsy findings of a 37‐year‐old man with a complex mosaic karyotype involving del(18p), monosomy 13, and trisomy 20

G. Hutchins, M. Halushka, K. Blakemore, 2005, American Journal of Medical Genetics. Part A.

TRPC1, a human homolog of a Drosophila store-operated channel.

A. Jeromin, C. Montell, G. Stetten, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Frequency of chromosomal abnormalities in spontaneous abortions derived from intracytoplasmic sperm injection compared with those from in vitro fertilization.

Yulian Zhao, W. Robinson, G. Stetten, 2006, Fertility and sterility.

Isolated fetal ascites detected by sonography: An unusual presentation of Turner syndrome

K. Blakemore, G. Stetten, J. Wax, 1992, Obstetrics and gynecology.

Prenatal Detection of a Subtle Unbalanced Chromosome Rearrangement by Karyotyping, FISH and Array Comparative Genomic Hybridization

K. Blakemore, G. Stetten, Daniel O. Saul, 2008, Fetal Diagnosis and Therapy.

Microphthalmia with linear skin defects (MLS) syndrome evaluated by prenatal karyotyping, FISH and array comparative genomic hybridization

A. Hamosh, K. Blakemore, G. Stetten, 2007, Prenatal diagnosis.

Molecular characterization of a deleted X chromosome (Xq13.3-Xq21.31) exhibiting random X inactivation

B. Migeon, J. Axelman, D. Dungy, 1995, Somatic cell and molecular genetics.

Prenatal diagnosis of mosaic trisomy 8q studied by ultrasound, cytogenetics, and array‐CGH

K. Blakemore, G. Stetten, Sarah N. Dowey, 2008, American journal of medical genetics. Part A.

Map location and gene structure of the Homo sapiens mitotic arrest deficient 2 (MAD2L1) gene at 4q27.

F. Spencer, K. Jeang, D. Jin, 1998, Genomics.

Prenatal detection of an unstable ring 21 chromosome

C. Boehm, G. Stetten, V. Corson, 1984, Human Genetics.

A reciprocal translocation 46,XY,t(8;9)(p11.2;q13) in a bladder exstrophy patient disrupts CNTNAP3 and presents evidence of a pericentromeric duplication on chromosome 9.

S. South, Ankita Patel, G. Stetten, 2005, Genomics.

Evidence for involvement of a Robertsonian translocation 13 chromosome in formation of a ring chromosome 13.

S. Antonarakis, K. Blakemore, G. Stetten, 1990, Molecular biology & medicine.

Prenatal detection of an accessory chromosome identified as an inversion duplication (15)

G. Stetten, V. Corson, Bernadette Sroka-Zaczek, 1981, Human Genetics.

Colcemid Sensitivity of Fission Yeast and the Isolation of Colcemid-Resistant Mutants

G. Stetten, S. Lederberg, 1970, Science.

33258 Hoechst enhancement of the photosensitivity of bromodeoxyuridine-substituted cells

S. Latt, G. Stetten, R. Davidson, 1976, Somatic cell genetics.

33258 Hoechst enhances the selectivity of the bromodeoxyuridine--light method of isolating conditional lethal mutants.

S. Latt, G. Stetten, R. Davidson, 1977, Experimental cell research.

Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study

S. Schwartz, U. Surti, L. Christ, 2006, Journal of Medical Genetics.

Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndrome

Jack C. Yu, E. Jabs, R. Norris, 2000, Mammalian Genome.

Sexual discordance in monozygotic twins.

G. Hutchins, W. Neuman, K. Blakemore, 1990, American journal of medical genetics.

Chromosomal disorders: background and neuroradiology.

A. J. Kumar, A. Reiss, T. Naidich, 1992, AJNR. American journal of neuroradiology.

Isolation and characterization of the human gene encoding Ito: further diversity by alternative mRNA splicing.

G. Tomaselli, G. Stetten, W. Kong, 1998, The American journal of physiology.

Isolation and characterization of the human gene encoding I to: further diversity by alternative mRNA splicing.

G. Tomaselli, G. Stetten, W. Kong, 1998, American journal of physiology. Heart and circulatory physiology.

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.

Unilateral Renal Hypoplasia And Contralateral Renal Agenesis: A New Association With 45,X/46,XY Mosaicism

G. Hutchins, K. Blakemore, G. Stetten, 1994, American Journal of Perinatology.

Prenatal identification of small mosaic markers of different chromosomal origins

E. Jabs, K. Blakemore, G. Stetten, 1992, Prenatal diagnosis.

UvA-DARE ( Digital Academic Repository ) Molecular biology and pharmacogenetics of x-linked adrenoleukodystrophy

J. Pevsner, P. Watkins, L. Braiterman, 2012 .