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A prevalent mutation for galactosemia among black Americans

The Journal of pediatrics, 1996, Vol.128 (1), p.89-95

1996

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Molecular basis for Duarte and Los Angeles variant galactosemia

American journal of human genetics, 1997-02, Vol.60 (2), p.366-372

1997

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A common mutation associated with the duarte galactosemia allele

American journal of human genetics, 1994-06, Vol.54 (6), p.1030-1036

1994

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Galactosemia: a strategy to identify new biochemical phenotypes and molecular genotypes

American journal of human genetics, 1995-03, Vol.56 (3), p.630-639

1995

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Detection of restriction fragment length polymorphisms in clinical isolates and serially passaged Pseudomonas aeruginosa strains

Journal of Clinical Microbiology, 1990-10, Vol.28 (10), p.2178-2182

1990

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The Duarte allele impairs biostability of galactose-1-phosphate uridyltransferase in human lymphoblasts

Human mutation, 1998, Vol.11 (1), p.28-38

1998

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Characterization of an unusual deletion of the galactose-1-phosphate uridyl transferase (GALT) gene

Genetics in medicine, 2006-10, Vol.8 (10), p.635-640

2006

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A molecular approach to galactosemia

European journal of pediatrics, 1995-01, Vol.154 (7 Suppl 2), p.S21-S27

1995

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Proof-Testing Graphite and Its Design Implications

Journal of the American Ceramic Society, 1965-07, Vol.48 (7), p.338-341

1965

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Galactosemia : a strategy to identify new biochemical phenotype and molecular genotypes

American journal of human genetics, 1995, Vol.56 (3), p.630-639

1995

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Rapid Clearance of Fetal DNA from Maternal Plasma

American journal of human genetics, 1999, Vol.64 (1), p.218-224

1999

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Prenatal Diagnosis of Fetal RhD Status by Molecular Analysis of Maternal Plasma

The New England journal of medicine, 1998-12, Vol.339 (24), p.1734-1738

1998

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Quantitative Analysis of Fetal DNA in Maternal Plasma and Serum: Implications for Noninvasive Prenatal Diagnosis

American journal of human genetics, 1998-04, Vol.62 (4), p.768-775

1998

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Lack of norovirus replication and histo-blood group antigen expression in 3-dimensional intestinal epithelial cells

Emerging infectious diseases, 2013-03, Vol.19 (3), p.431-438

2013

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Mean Diffusional Kurtosis in Patients with Glioma: Initial Results with a Fast Imaging Method in a Clinical Setting

American journal of neuroradiology : AJNR, 2015-08, Vol.36 (8), p.1472-1478

2015

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Plasma DNA as a Prognostic Marker in Trauma Patients

Clinical chemistry (Baltimore, Md.), 2000-03, Vol.46 (3), p.319-323

2000

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Quantitative analysis of cell-free Epstein-Barr virus DNA in plasma of patients with nasopharyngeal carcinoma

Cancer research (Chicago, Ill.), 1999-03, Vol.59 (6), p.1188-1191

1999

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Presence of donor-specific DNA in plasma of kidney and liver-transplant recipients

The Lancet (British edition), 1998-05, Vol.351 (9112), p.1329-1330

1998

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Maternal plasma fetal DNA as a marker for preterm labour

The Lancet (British edition), 1998-12, Vol.352 (9144), p.1904-1905

1998

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Increased Fetal DNA Concentrations in the Plasma of Pregnant Women Carrying Fetuses with Trisomy 21

Clinical chemistry (Baltimore, Md.), 1999-10, Vol.45 (10), p.1747-1751

1999

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Detection of aberrant p16 methylation in the plasma and serum of liver cancer patients

Cancer research (Chicago, Ill.), 1999, Vol.59 (1), p.71-73

1999

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Integrative epigenome-wide analysis demonstrates that DNA methylation may mediate genetic risk in inflammatory bowel disease

Nature communications, 2016-11, Vol.7 (1), p.13507-13507, Article 13507

2016

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Quantitative and temporal correlation between circulating cell-free Epstein-Barr virus DNA and tumor recurrence in nasopharyngeal carcinoma

Cancer research (Chicago, Ill.), 1999-11, Vol.59 (21), p.5452-5455

1999

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Determination of the bonding strength in solid oxide fuel cells’ interfaces by Schwickerath crack initiation test

Journal of the European Ceramic Society, 2017-09, Vol.37 (11), p.3565-3578

2017

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A prevalent mutation for galactosemia among black Americans

Molecular basis for Duarte and Los Angeles variant galactosemia

A common mutation associated with the duarte galactosemia allele

Galactosemia: a strategy to identify new biochemical phenotypes and molecular genotypes

Detection of restriction fragment length polymorphisms in clinical isolates and serially passaged Pseudomonas aeruginosa strains

The Duarte allele impairs biostability of galactose-1-phosphate uridyltransferase in human lymphoblasts

Characterization of an unusual deletion of the galactose-1-phosphate uridyl transferase (GALT) gene

A molecular approach to galactosemia

Naissance des sciences de la population

Proof-Testing Graphite and Its Design Implications

Galactosemia : a strategy to identify new biochemical phenotype and molecular genotypes

Rapid Clearance of Fetal DNA from Maternal Plasma

Prenatal Diagnosis of Fetal RhD Status by Molecular Analysis of Maternal Plasma

Quantitative Analysis of Fetal DNA in Maternal Plasma and Serum: Implications for Noninvasive Prenatal Diagnosis

Lack of norovirus replication and histo-blood group antigen expression in 3-dimensional intestinal epithelial cells

Mean Diffusional Kurtosis in Patients with Glioma: Initial Results with a Fast Imaging Method in a Clinical Setting

Plasma DNA as a Prognostic Marker in Trauma Patients

Quantitative analysis of cell-free Epstein-Barr virus DNA in plasma of patients with nasopharyngeal carcinoma

Presence of donor-specific DNA in plasma of kidney and liver-transplant recipients

Maternal plasma fetal DNA as a marker for preterm labour

Increased Fetal DNA Concentrations in the Plasma of Pregnant Women Carrying Fetuses with Trisomy 21

Detection of aberrant p16 methylation in the plasma and serum of liver cancer patients

Integrative epigenome-wide analysis demonstrates that DNA methylation may mediate genetic risk in inflammatory bowel disease

Quantitative and temporal correlation between circulating cell-free Epstein-Barr virus DNA and tumor recurrence in nasopharyngeal carcinoma

Determination of the bonding strength in solid oxide fuel cells’ interfaces by Schwickerath crack initiation test

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