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Molecular cloning and physical and genetic mapping of a novel human Na +/H + exchanger (NHE5/SLC9A5) to chromosome 16q22.1

Genomics (San Diego, Calif.), 1995-02, Vol.25 (3), p.615-622

1995

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Allogeneic hematopoietic cell transplantation for metastatic renal cell carcinoma after nonmyeloablative conditioning: Toxicity, clinical response, and immunological response to minor histocompatibility antigens

Clinical cancer research, 2004-12, Vol.10 (23), p.7799-7811

2004

Volltextzugriff (PDF)

Identification of a Herpes Simplex Labialis Susceptibility Region on Human Chromosome 21

The Journal of infectious diseases, 2008-02, Vol.197 (3), p.340-346

2008

Volltextzugriff (PDF)

Molecular Cloning and Physical and Genetic Mapping of the Human Anion Exchanger Isoform 3 (SLC2C) Gene to Chromosome 2q36

Genomics (San Diego, Calif.), 1994-08, Vol.22 (3), p.605-609

1994

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Localization to chromosome 22 of a gene encoding a human minor histocompatibility antigen

The Journal of immunology (1950), 1996-12, Vol.157 (12), p.5448

1996

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Feasibility of using genetic linkage analysis to identify the genes encoding T cell-defined minor histocompatibility antigens

Tissue antigens, 2002-04, Vol.59 (4), p.293-303

2002

Volltextzugriff (PDF)

Dinucleotide repeat polymorphism from a cosmid containing the human anion exchanger isoform 3 (SLC2C) gene

Human molecular genetics, 1994-11, Vol.3 (11), p.2086-2086

1994

Volltextzugriff (PDF)

Molecular cloning and physical and genetic mapping of a novel human Na super(+)/H super(+) exchanger (NHE5/SLC9A5) to chromosome 16q22.1

Genomics (San Diego, Calif.), 1995-01, Vol.25 (3), p.615-622

1995

Volltextzugriff (PDF)

Molecular cloning and physical and genetic mapping of the human anion exchanger isoform 3 (SLC2C) gene to chromosome 2q36

Genomics (San Diego, Calif.), 1994-01, Vol.27 (3), p.605-609

1994

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Exome analysis of a family with pleiotropic congenital heart disease

Circulation. Cardiovascular genetics, 2012-04, Vol.5 (2), p.175

2012

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A frameshift polymorphism in P2X5 elicits an allogeneic cytotoxic T lymphocyte response associated with remission of chronic myeloid leukemia

The Journal of clinical investigation, 2005-12, Vol.115 (12), p.3506-3516

2005

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A locus for febrile seizures (FEB3) maps to chromosome 2q23-24

Annals of neurology, 1999-10, Vol.46 (4), p.671-678

1999

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Genetic Mapping of Ossification of the Posterior Longitudinal Ligament of the Spine

American journal of human genetics, 1998-06, Vol.62 (6), p.1460-1467

1998

Volltextzugriff (PDF)

Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia : evidence for locus heterogeneity

American journal of human genetics, 1993-07, Vol.53 (1), p.193-200

1993

Volltextzugriff (PDF)

The identical 5' splice-site acceptor mutation in five attenuated APC families from Newfoundland demonstrates a founder effect

Human genetics, 1999-11, Vol.105 (5), p.388-398

1999

Volltextzugriff (PDF)

Identification of a Herpes Simplex Labialis Susceptibility Region on Human Chromosome 21. Commentary

The Journal of infectious diseases, 2008, Vol.197 (3)

2008

Volltextzugriff (PDF)

Linkage of a Familial Platelet Disorder With a Propensity to Develop Myeloid Malignancies to Human Chromosome 21q22.1-22.2

Blood, 1996-06, Vol.87 (12), p.5218-5224

1996

Volltextzugriff (PDF)

Genetic Linkage of the Dentinogenesis Imperfecta Type III Locus to Chromosome 4q

Journal of dental research, 1999-06, Vol.78 (6), p.1277-1282

1999

Volltextzugriff (PDF)

Analysis of microtubule-associated protein 1a gene in hereditary spastic paraplegia

Neurology, 1998-11, Vol.51 (5), p.1509

1998

Volltextzugriff (PDF)

The identical 5? splice-site acceptor mutation in five attenuated APC families from Newfoundland demonstrates a founder effect

Human genetics, 2000-09, Vol.107 (3), p.294-294

2000

Volltextzugriff (PDF)

Genetic mapping of adrenergic receptor genes in humans

Journal of molecular medicine (Berlin, Germany), 1995-06, Vol.73 (6), p.299-306

1995

Volltextzugriff (PDF)

The identical 5' splice-site acceptor mutation in five attenuated APC families from newfoundiand demonstrates a founder effect

Human genetics, 1999, Vol.105 (5), p.388-398

1999

Volltextzugriff (PDF)

The identical 5' splice-site acceptor mutation in five attenuated APC families from Newfoundland demonstrates a founder effect

Human genetics, 1999-11, Vol.105 (5), p.388-398

1999

Volltextzugriff (PDF)

Genetic linkage of the human gene for phenylethanol-amine N-methyltransferase (PNMT), the adrenaline-synthesizing enzyme, to DNA markers on chromosome 17q21–q22

Human molecular genetics, 1992-06, Vol.1 (3), p.175-178

1992

Volltextzugriff (PDF)

Aminoaciduria in chronic renal failure--its relationship to vitamin D and parathyroid status

The American journal of clinical nutrition, 1980-07, Vol.33 (7), p.1541-1545

1980

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Molecular cloning and physical and genetic mapping of a novel human Na +/H + exchanger (NHE5/SLC9A5) to chromosome 16q22.1

Allogeneic hematopoietic cell transplantation for metastatic renal cell carcinoma after nonmyeloablative conditioning: Toxicity, clinical response, and immunological response to minor histocompatibility antigens

Identification of a Herpes Simplex Labialis Susceptibility Region on Human Chromosome 21

Molecular Cloning and Physical and Genetic Mapping of the Human Anion Exchanger Isoform 3 (SLC2C) Gene to Chromosome 2q36

Localization to chromosome 22 of a gene encoding a human minor histocompatibility antigen

Feasibility of using genetic linkage analysis to identify the genes encoding T cell-defined minor histocompatibility antigens

Dinucleotide repeat polymorphism from a cosmid containing the human anion exchanger isoform 3 (SLC2C) gene

Molecular cloning and physical and genetic mapping of a novel human Na super(+)/H super(+) exchanger (NHE5/SLC9A5) to chromosome 16q22.1

Molecular cloning and physical and genetic mapping of the human anion exchanger isoform 3 (SLC2C) gene to chromosome 2q36

Exome analysis of a family with pleiotropic congenital heart disease

A frameshift polymorphism in P2X5 elicits an allogeneic cytotoxic T lymphocyte response associated with remission of chronic myeloid leukemia

A locus for febrile seizures (FEB3) maps to chromosome 2q23-24

Genetic Mapping of Ossification of the Posterior Longitudinal Ligament of the Spine

Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia : evidence for locus heterogeneity

The identical 5' splice-site acceptor mutation in five attenuated APC families from Newfoundland demonstrates a founder effect

Identification of a Herpes Simplex Labialis Susceptibility Region on Human Chromosome 21. Commentary

Linkage of a Familial Platelet Disorder With a Propensity to Develop Myeloid Malignancies to Human Chromosome 21q22.1-22.2

Genetic Linkage of the Dentinogenesis Imperfecta Type III Locus to Chromosome 4q

Analysis of microtubule-associated protein 1a gene in hereditary spastic paraplegia

The identical 5? splice-site acceptor mutation in five attenuated APC families from Newfoundland demonstrates a founder effect

Genetic mapping of adrenergic receptor genes in humans

The identical 5' splice-site acceptor mutation in five attenuated APC families from newfoundiand demonstrates a founder effect

The identical 5' splice-site acceptor mutation in five attenuated APC families from Newfoundland demonstrates a founder effect

Genetic linkage of the human gene for phenylethanol-amine N-methyltransferase (PNMT), the adrenaline-synthesizing enzyme, to DNA markers on chromosome 17q21–q22

Aminoaciduria in chronic renal failure--its relationship to vitamin D and parathyroid status

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