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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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Mutation and expression analysis of human BUB1 and BUB1B in aneuploid breast cancer cell lines

Cancer letters, 2000-05, Vol.152 (2), p.193-199

2000

Volltextzugriff (PDF)

Mutant deoxynucleotide carrier is associated with congenital microcephaly

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

2002

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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

Cytogenetics and cell genetics, 1996, Vol.72 (4), p.319

1996

Volltextzugriff (PDF)

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

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

2001

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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

Volltextzugriff (PDF)

Successful bone marrow transplantation in a patient with Schimke immuno-osseous dysplasia

The Journal of pediatrics, 2000-12, Vol.137 (6), p.882-886

2000

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Risk Assessment and Presymptomatic Molecular Diagnosis in Hereditary Breast Cancer

Clinics in laboratory medicine, 1996-03, Vol.16 (1), p.139-167

1996

Volltextzugriff (PDF)

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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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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Genetic risk factors for melanoma in children

The Journal of pediatrics, 1994-12, Vol.125 (6), p.1015-1015

Petty, Elizabeth Marie

1994

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Ornithine transcarbamylase polymorphism detected by PCR introduction of Dral site

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

1991

Volltextzugriff (PDF)

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

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

2004

Volltextzugriff (PDF)

Smallest terminal deletion of the long arm of chromosome 2 in a mildly affected boy

American journal of medical genetics, 1992-11, Vol.44 (4), p.500-502

1992

Volltextzugriff (PDF)

Previously unrecognized congenital progeroid disorder

American journal of medical genetics, 1990-03, Vol.35 (3), p.383-387

1990

Volltextzugriff (PDF)

Ornithine transcarbamylase polymorphism detected by PCR introduction of DraI site

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

1991

Volltextzugriff (PDF)

Cutaneous malignant melanoma and atypical moles associated with a constitutional rearrangement of chromosomes 5 and 9

American journal of medical genetics, 1993-01, Vol.45 (1), p.77-80

1993

Volltextzugriff (PDF)

Klippel-Feil sequence and sleep-disordered breathing in two children

The American review of respiratory disease, 1993-01, Vol.147 (1), p.202

1993

Volltextzugriff (PDF)

Mosaic dup (9p) diagnosed by fluorescence in situ hybridization (FISH)

American journal of medical genetics, 1993-03, Vol.45 (6), p.770-773

1993

Volltextzugriff (PDF)

Attitudes of young adults to prenatal screening and genetic correction for human attributes and psychiatric conditions

American journal of medical genetics, 1998-03, Vol.76 (2), p.111-119

1998

Volltextzugriff (PDF)

Characterization of a stapes ankylosis family with a NOG mutation

Otology & neurotology, 2003-03, Vol.24 (2), p.210

2003

Volltextzugriff (PDF)

Systemic lupus erythematosus in a man with Noonan syndrome

American journal of medical genetics, 2001-07, Vol.102 (1), p.59-62

2001

Volltextzugriff (PDF)

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MicroRNAs in development and disease

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

Mutation and expression analysis of human BUB1 and BUB1B in aneuploid breast cancer cell lines

Mutant deoxynucleotide carrier is associated with congenital microcephaly

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

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

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

Successful bone marrow transplantation in a patient with Schimke immuno-osseous dysplasia

Risk Assessment and Presymptomatic Molecular Diagnosis in Hereditary Breast Cancer

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

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

Genetic risk factors for melanoma in children

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

Smallest terminal deletion of the long arm of chromosome 2 in a mildly affected boy

Previously unrecognized congenital progeroid disorder

Ornithine transcarbamylase polymorphism detected by PCR introduction of DraI site

Cutaneous malignant melanoma and atypical moles associated with a constitutional rearrangement of chromosomes 5 and 9

Klippel-Feil sequence and sleep-disordered breathing in two children

Mosaic dup (9p) diagnosed by fluorescence in situ hybridization (FISH)

Attitudes of young adults to prenatal screening and genetic correction for human attributes and psychiatric conditions

Characterization of a stapes ankylosis family with a NOG mutation

Systemic lupus erythematosus in a man with Noonan syndrome

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