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MicroRNAs in development and disease

Clinical genetics, 2008-10, Vol.74 (4), p.296-306

2008

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Conquering the complex world of human septins: implications for health and disease

Clinical genetics, 2010-06, Vol.77 (6), p.511-524

2010

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PRAD1, a candidate BCL1 oncogene: mapping and expression in centrocytic lymphoma

Proceedings of the National Academy of Sciences - PNAS, 1991-11, Vol.88 (21), p.9638-9642

1991

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Fusion of a novel gene, RCC17, to the TFE3 gene in t(X;17)(p11.2;q25.3)-bearing papillary renal cell carcinomas

Cancer research (Chicago, Ill.), 2001-05, Vol.61 (10), p.4130-4135

2001

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Isolation and mapping of a human septin gene to a region on chromosome 17q, commonly deleted in sporadic epithelial ovarian tumors

Cancer research (Chicago, Ill.), 2000-09, Vol.60 (17), p.4729-4734

2000

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Understandings of Basic Genetics in the United States: Results from a National Survey of Black and White Men and Women

Public health genomics, 2010-01, Vol.13 (7/8), p.467-476

2010

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Novel autosomal dominant mandibulofacial dysostosis with ptosis: clinical description and exclusion of TCOF1

Journal of medical genetics, 2002-07, Vol.39 (7), p.484-488

2002

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Mutant deoxynucleotide carrier is associated with congenital microcephaly

Nature genetics, 2002-09, Vol.32 (1), p.175-179

2002

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A region of interstitial 17q25 allelic loss in ovarian tumors coincides with a defined region of loss in breast tumors

Oncogene, 1997-04, Vol.14 (16), p.1991-1994

1997

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Characterisation and genetic mapping of a new X linked deafness syndrome

Journal of medical genetics, 2000-11, Vol.37 (11), p.836-841

2000

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Assignment of a Locus for Familial Melanoma, MLM, to Chromosome 9p13-p22

Science (American Association for the Advancement of Science), 1992-11, Vol.258 (5085), p.1148-1152

1992

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FISH localization of the soluble thymidine kinase gene (TK1) to human 17q25, a region of chromosomal loss in sporadic breast tumors

Cytogenetic and genome research, 1996-01, Vol.72 (4), p.319-321

1996

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Absence of PTEN Germ-Line Mutations in Men with a Potential Inherited Predisposition to Prostate Cancer

Clinical cancer research, 1999-06, Vol.5 (6), p.1387-1391

1999

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BRCA1 mutation testing: controversies and challenges

Clinical chemistry (Baltimore, Md.), 1997-01, Vol.43 (1), p.6-8

1997

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Virtual genome scan: a tool for restriction landmark-based scanning of the human genome

Genome research, 2001-08, Vol.11 (8), p.1453-1459

2001

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miRNAs and cancer: New research developments and potential clinical applications

Cancer biology & therapy, 2009-12, Vol.8 (24), p.2317-2322

2009

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Genomic characterization of human SEC14L1 splice variants within a 17q25 candidate tumor suppressor gene region and identification of an unrelated embedded expressed sequence tag

Mammalian genome, 2001-12, Vol.12 (12), p.925-929

2001

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Overexpressed genes/ESTs and characterization of distinct amplicons on 17q23 in breast cancer cells

Neoplasia (New York, N.Y.), 2001-11, Vol.3 (6), p.521-526

2001

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White Americans' Genetic Lay Theories of Race Differences and Sexual Orientation: Their Relationship with Prejudice toward Blacks, and Gay Men and Lesbians

Group processes & intergroup relations, 2006-01, Vol.9 (1), p.77-94

2006

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The Western New York Health Resources Project : developing access to local health information

Bulletin of the Medical Library Association, 1998-07, Vol.86 (3), p.335-339

1998

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Distal chromosome 17q loss in Barrett's esophageal and gastric cardia adenocarcinomas: Implications for tumorigenesis

Molecular carcinogenesis, 1998-08, Vol.22 (4), p.222-228

1998

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Detailed deletion analysis of sporadic breast tumors defines an interstitial region of allelic loss on 17q25

Genes chromosomes & cancer, 1996-09, Vol.17 (1), p.64-68

1996

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Expression and mutational analyses of the human MAD2L1 gene in breast cancer cells

Genes chromosomes & cancer, 2000-12, Vol.29 (4), p.356-362

2000

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Ornithine transcarbamylase polymorphism detected by PCR introduction of Dral site

Nucleic acids research, 1991-02, Vol.19 (3), p.690-690

1991

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CHFR-associated early G sub(2)/M checkpoint defects in breast cancer cells

Molecular carcinogenesis, 2004-01, Vol.39 (1), p.26-33

2004

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MicroRNAs in development and disease

Conquering the complex world of human septins: implications for health and disease

PRAD1, a candidate BCL1 oncogene: mapping and expression in centrocytic lymphoma

Fusion of a novel gene, RCC17, to the TFE3 gene in t(X;17)(p11.2;q25.3)-bearing papillary renal cell carcinomas

Isolation and mapping of a human septin gene to a region on chromosome 17q, commonly deleted in sporadic epithelial ovarian tumors

Understandings of Basic Genetics in the United States: Results from a National Survey of Black and White Men and Women

Novel autosomal dominant mandibulofacial dysostosis with ptosis: clinical description and exclusion of TCOF1

Mutant deoxynucleotide carrier is associated with congenital microcephaly

A region of interstitial 17q25 allelic loss in ovarian tumors coincides with a defined region of loss in breast tumors

Characterisation and genetic mapping of a new X linked deafness syndrome

Assignment of a Locus for Familial Melanoma, MLM, to Chromosome 9p13-p22

FISH localization of the soluble thymidine kinase gene (TK1) to human 17q25, a region of chromosomal loss in sporadic breast tumors

Absence of PTEN Germ-Line Mutations in Men with a Potential Inherited Predisposition to Prostate Cancer

BRCA1 mutation testing: controversies and challenges

Virtual genome scan: a tool for restriction landmark-based scanning of the human genome

miRNAs and cancer: New research developments and potential clinical applications

Genomic characterization of human SEC14L1 splice variants within a 17q25 candidate tumor suppressor gene region and identification of an unrelated embedded expressed sequence tag

Overexpressed genes/ESTs and characterization of distinct amplicons on 17q23 in breast cancer cells

White Americans' Genetic Lay Theories of Race Differences and Sexual Orientation: Their Relationship with Prejudice toward Blacks, and Gay Men and Lesbians

The Western New York Health Resources Project : developing access to local health information

Distal chromosome 17q loss in Barrett's esophageal and gastric cardia adenocarcinomas: Implications for tumorigenesis

Detailed deletion analysis of sporadic breast tumors defines an interstitial region of allelic loss on 17q25

Expression and mutational analyses of the human MAD2L1 gene in breast cancer cells

Ornithine transcarbamylase polymorphism detected by PCR introduction of Dral site

CHFR-associated early G sub(2)/M checkpoint defects in breast cancer cells

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