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Results of screening 1.9 million Texas newborns for 21-hydroxylase-deficient congenital adrenal hyperplasia

Pediatrics (Evanston), 1998-04, Vol.101 (4 Pt 1), p.583

1998

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Committee report: Considerations and recommendations for national guidance regarding the retention and use of residual dried blood spot specimens after newborn screening

Genetics in medicine, 2011-07, Vol.13 (7), p.621-624

2011

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U.S. Newborn Screening Policy Dilemmas for the Twenty-First Century

Molecular Genetics and Metabolism, 2001-09, Vol.74 (1-2), p.64-74

Therrell, Bradford L.

2001

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Demographic Risk Factors Associated with Elevated Lead Levels in Texas Children Covered by Medicaid

Environmental health perspectives, 1997-01, Vol.105 (1), p.66-68

1997

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Assuring clinical genetic services for newborns identified through U.S. newborn screening programs

Genetics in medicine, 2007-08, Vol.9 (8), p.518-527

2007

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An evaluation of kits for measuring thyrotropin in newborns

Clinical chemistry (Baltimore, Md.), 1984-11, Vol.30 (11), p.1854

1984

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Effect of lot-to-lot variability in filter paper on the quantification of thyroxin, thyrotropin, and phenylalanine in dried-blood specimens

Clinical chemistry (Baltimore, Md.), 1988-01, Vol.34 (1), p.53

1988

Volltextzugriff (PDF)

Neuroblastoma screening in the United States: Results of the Texas outreach program for neuroblastoma screening

Cancer, 1998-04, Vol.82 (8), p.1593-1602

1998

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Structural and functional studies of Hemoglobin Wayne: An elongated α-chain variant

Journal of molecular biology, 1984-12, Vol.180 (4), p.1119-1140

1984

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Genotypic confirmation from the original dried blood specimens in a neonatal hemoglobinopathy screening program

Pediatric research, 1992-03, Vol.31 (3), p.217-221

1992

Volltextzugriff (PDF)

Analysis for lead in undiluted whole blood by tantalum ribbon atomic absorption spectrophotometry

Clinical chemistry (Baltimore, Md.), 1978-07, Vol.24 (7), p.1182

1978

Volltextzugriff (PDF)

Syphla-Chek: a qualitative study

Journal of Clinical Microbiology, 1977-06, Vol.5 (6), p.593-595

1977

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Multivariant Confirmation of Sickle Cell Disease Using a Non-Radioactive Minisequencing Reaction

Hemoglobin, 1997, Vol.21 (1), p.71-89

1997

Volltextzugriff (PDF)

Experiences with sickle hemoglobin testing in the Texas Newborn Screening Program

Pediatrics (Evanston), 1989-05, Vol.83 (5 Pt 2), p.864

1989

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Unbiased analysis of the frequency of beta-thalassemia point mutations in a population of African-American newborns

Archives of pathology & laboratory medicine (1976), 1993-11, Vol.117 (11), p.1110

1993

Volltextzugriff (PDF)

Rapid detection of beta s DNA from Guthrie cards by chromogenic probes

The Lancet (British edition), 1989-09, Vol.2 (8665), p.741-741

1989

Volltextzugriff (PDF)

Second testing for hypothyroidism

Pediatrics (Evanston), 1986-08, Vol.78 (2), p.375

1986

Volltextzugriff (PDF)

Application of Molecular Genetics in Public Health: Improved Follow-up in a Neonatal Hemoglobinopathy Screening Program

Biochemical medicine and metabolic biology, 1994-06, Vol.52 (1), p.27-35

1994

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Hemoglobin Rio Grande [β8 (A5) Lys→Thr] A New Variant Found in A Mexican-American Family

Hemoglobin, 1983, Vol.7 (1), p.91-95

1983

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Hemoglobin P Nilotic in a Mexican-American Family

Hemoglobin, 1978, Vol.2 (1), p.65-69

1978

Volltextzugriff (PDF)

Hemoglobin Cubujuqui (α141 ARG-SER): Functional Consequences of the Alteration of the C-Terminus of the αChain of Hemoglobin

Hemoglobin, 1981, Vol.5 (7-8), p.715-724

1981

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Hemoglobins Austin and Waco: two hemoglobins with substitutions in the alpha 1 beta 2 contact region

Archives of biochemistry and biophysics, 1977-02, Vol.179 (1), p.86-94

1977

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Hemoglobin Lufkin: beta 29 (B11) Gly replaced by Asp. An unstable hemoglobin variant involving an internal amino acid residue

Hemoglobin, 1977, Vol.1 (8), p.799-814

1977

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History and Current Status of Newborn Screening for Hemoglobinopathies

Seminars in perinatology, 2010-04, Vol.34 (2), p.134-144

2010

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Hemoglobin Fannin-Lubbock [alpha2 beta 2 119 (GH2) Gly replaced by Asp]. A new hemoglobin variant at the alpha1 beta 1 contact

Biochimica et biophysica acta, 1976-12, Vol.453 (2), p.472

1976

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Results of screening 1.9 million Texas newborns for 21-hydroxylase-deficient congenital adrenal hyperplasia

Committee report: Considerations and recommendations for national guidance regarding the retention and use of residual dried blood spot specimens after newborn screening

U.S. Newborn Screening Policy Dilemmas for the Twenty-First Century

Demographic Risk Factors Associated with Elevated Lead Levels in Texas Children Covered by Medicaid

Assuring clinical genetic services for newborns identified through U.S. newborn screening programs

An evaluation of kits for measuring thyrotropin in newborns

Effect of lot-to-lot variability in filter paper on the quantification of thyroxin, thyrotropin, and phenylalanine in dried-blood specimens

Neuroblastoma screening in the United States: Results of the Texas outreach program for neuroblastoma screening

Structural and functional studies of Hemoglobin Wayne: An elongated α-chain variant

Genotypic confirmation from the original dried blood specimens in a neonatal hemoglobinopathy screening program

Analysis for lead in undiluted whole blood by tantalum ribbon atomic absorption spectrophotometry

Syphla-Chek: a qualitative study

Multivariant Confirmation of Sickle Cell Disease Using a Non-Radioactive Minisequencing Reaction

Experiences with sickle hemoglobin testing in the Texas Newborn Screening Program

Unbiased analysis of the frequency of beta-thalassemia point mutations in a population of African-American newborns

Rapid detection of beta s DNA from Guthrie cards by chromogenic probes

Second testing for hypothyroidism

Application of Molecular Genetics in Public Health: Improved Follow-up in a Neonatal Hemoglobinopathy Screening Program

Hemoglobin Rio Grande [β8 (A5) Lys→Thr] A New Variant Found in A Mexican-American Family

Hemoglobin P Nilotic in a Mexican-American Family

Hemoglobin Cubujuqui (α141 ARG-SER): Functional Consequences of the Alteration of the C-Terminus of the αChain of Hemoglobin

Hemoglobins Austin and Waco: two hemoglobins with substitutions in the alpha 1 beta 2 contact region

Hemoglobin Lufkin: beta 29 (B11) Gly replaced by Asp. An unstable hemoglobin variant involving an internal amino acid residue

History and Current Status of Newborn Screening for Hemoglobinopathies

Hemoglobin Fannin-Lubbock [alpha2 beta 2 119 (GH2) Gly replaced by Asp]. A new hemoglobin variant at the alpha1 beta 1 contact

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