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Assignment of the human heart tetrodotoxin-resistant voltage-gated Na+ channel alpha-subunit gene (SCN5A) to band 3p21

Cytogenetics and cell genetics, 1995-01, Vol.68 (1-2), p.67

1995

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Chromosome 1p terminal deletion: report of new findings and confirmation of two characteristic phenotypes

Journal of medical genetics, 1995-08, Vol.32 (8), p.619-622

1995

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The Primary Erythermalgia–Susceptibility Gene Is Located on Chromosome 2q31-32

American journal of human genetics, 2001-05, Vol.68 (5), p.1277-1282

2001

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Pre-B Cell Leukemia Associated With Chromosome Translocation 1; 19

Blood, 1984-03, Vol.63 (3), p.721-724

1984

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Nutrient levels in amniotic fluid from women with normal and neural tube defect pregnancies

Biology of the neonate, 1992, Vol.61 (4), p.226

1992

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Terminal deletion of the long arm of chromosome 4 in a mother and two sons

Clinical genetics, 1996-12, Vol.50 (6), p.538-540

1996

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Over-representation of the disease associated (CAG) and (CGG) repeats in the human genome

Nucleic acids research, 1994-05, Vol.22 (9), p.1735-1740

1994

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Relationship between amniotic fluid and maternal blood nutrient levels

Journal of perinatal medicine, 1994, Vol.22 (3), p.227

1994

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Autosomal dominant erythromelalgia

American journal of medical genetics, 1992-02, Vol.42 (3), p.310-315

1992

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Assignment of a Human Voltage-Dependent Sodium Channel α-Subunit Gene (SCN6A) to 2q21-q23

Genomics (San Diego, Calif.), 1994-01, Vol.19 (2), p.395-397

1994

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A complex chromosome rearrangement resulting in trisomy 15q22→qter

Journal of medical genetics, 1982-06, Vol.19 (3), p.224-227

1982

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Survey of medical genetics personnel

American journal of human genetics, 1987-04, Vol.40 (4), p.374-377

1987

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Decreased levels of amniotic fluid α-fetoprotein associated with Down syndrome

American journal of obstetrics and gynecology, 1985-11, Vol.153 (5), p.541-544

1985

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High resolution cytogenetic evaluation of couples with recurring fetal wastage

Human genetics, 1985-01, Vol.69 (3), p.246-249

1985

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Interstitial deletion of chromosome 1 [del(1)(q25q32)] in an infant with prune belly sequence

Prenatal diagnosis, 1988-03, Vol.8 (3), p.169-174

1988

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Molecular and cytogenetic investigation of complex tissue-specific duplication and loss of chromosome 21 in a child with a monosomy 21 phenotype

American journal of medical genetics, 1992-06, Vol.43 (3), p.554-560

1992

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Congenital heart disease in infants with Down's syndrome

Southern medical journal (Birmingham, Ala.), 1994-07, Vol.87 (7), p.724-727

1994

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A de novo 3p;8p unbalanced translocation resulting in partial dup(3p) and partial del(8p)

Journal of medical genetics, 1987-03, Vol.24 (3), p.174-177

1987

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Effect of drugs on chromosome structure

The American journal of clinical nutrition, 1975-05, Vol.28 (5), p.521-529

Finley, WH

1975

Volltextzugriff (PDF)

Delivering genetic services

Pediatric annals, 1978-06, Vol.7 (6), p.13

Finley, W H

1978

Volltextzugriff (PDF)

Increased Chromosome Number of Rat Parotid Cells After Isoproterenol.

Proceedings of the Society for Experimental Biology and Medicine, 1967-07, Vol.125 (3), p.722-728

1967

Volltextzugriff (PDF)

Genetic screening: an overview

The Alabama journal of medical sciences, 1982-04, Vol.19 (2), p.147

Finley, W H

1982

Volltextzugriff (PDF)

Birth defects surveillance: Jefferson County, Alabama, and Uppsala County, Sweden

Southern medical journal (Birmingham, Ala.), 1994-04, Vol.87 (4), p.440-445

1994

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An extra small metacentric chromosome in association with multiple congenital abnormalities

Journal of medical genetics, 1971-09, Vol.8 (3), p.381-383

1971

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IgA ABSENCE ASSOCIATED WITH A RING-18 CHROMOSOME

The Lancet (British edition), 1968-01, Vol.291 (7551), p.1095-1096

1968

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Assignment of the human heart tetrodotoxin-resistant voltage-gated Na+ channel alpha-subunit gene (SCN5A) to band 3p21

Chromosome 1p terminal deletion: report of new findings and confirmation of two characteristic phenotypes

The Primary Erythermalgia–Susceptibility Gene Is Located on Chromosome 2q31-32

Pre-B Cell Leukemia Associated With Chromosome Translocation 1; 19

Nutrient levels in amniotic fluid from women with normal and neural tube defect pregnancies

Terminal deletion of the long arm of chromosome 4 in a mother and two sons

Over-representation of the disease associated (CAG) and (CGG) repeats in the human genome

Relationship between amniotic fluid and maternal blood nutrient levels

Autosomal dominant erythromelalgia

Assignment of a Human Voltage-Dependent Sodium Channel α-Subunit Gene (SCN6A) to 2q21-q23

A complex chromosome rearrangement resulting in trisomy 15q22→qter

Survey of medical genetics personnel

Decreased levels of amniotic fluid α-fetoprotein associated with Down syndrome

High resolution cytogenetic evaluation of couples with recurring fetal wastage

Interstitial deletion of chromosome 1 [del(1)(q25q32)] in an infant with prune belly sequence

Molecular and cytogenetic investigation of complex tissue-specific duplication and loss of chromosome 21 in a child with a monosomy 21 phenotype

Congenital heart disease in infants with Down's syndrome

A de novo 3p;8p unbalanced translocation resulting in partial dup(3p) and partial del(8p)

Effect of drugs on chromosome structure

Delivering genetic services

Increased Chromosome Number of Rat Parotid Cells After Isoproterenol.

Genetic screening: an overview

Birth defects surveillance: Jefferson County, Alabama, and Uppsala County, Sweden

An extra small metacentric chromosome in association with multiple congenital abnormalities

IgA ABSENCE ASSOCIATED WITH A RING-18 CHROMOSOME

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