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Unfulfilled sterilization requests: what happens 6 months later?

Contraception (Stoneham), 2012-09, Vol.86 (3), p.323-323

2012

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Severe limb abnormalities after chorion villus sampling at 56-66 days' gestation

The Lancet (British edition), 1991-03, Vol.337 (8744), p.762-763

1991

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Physical mapping across the fragile X: Hypermethylation and clinical expression of the fragile X syndrome

Cell, 1991-02, Vol.64 (4), p.861-866

1991

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Clinical features and molecular analysis of the α thalassemia/mental retardation syndromes. I, Cases due to deletions involving chromosome band 16p13.3

American journal of human genetics, 1990-06, Vol.46 (6), p.1112-1116

1990

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Molecular studies of trisomy 18

American journal of human genetics, 1993-06, Vol.52 (6), p.1139-1144

1993

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Clinical features and molecular analysis of the α thalassemia/mental retardation syndromes. II, Cases without detectable abnormality of the α globin complex

American journal of human genetics, 1990-06, Vol.46 (6), p.1127-1140

1990

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Unusual segregation of constitutional 11q;22q translocation may be explained by crossover in interchange segment, followed by 3 : 1 segregation at meiosis I

Human genetics, 1990-06, Vol.85 (1), p.143-143

LINDENBAUM, R. H

1990

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UK clinicians' knowledge of and attitudes to the prenatal diagnosis of single gene disorders

Journal of medical genetics, 1992-01, Vol.29 (1), p.20-23

1992

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Parental decisions regarding termination of pregnancy following prenatal detection of sex chromosome abnormality

Prenatal diagnosis, 1987-05, Vol.7 (4), p.239-244

1987

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Prevalence of Huntington's disease among UK immigrants from the Indian subcontinent

British journal of psychiatry, 1990-10, Vol.157 (4), p.598-599

1990

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Tuberous sclerosis: a new estimate of prevalence within the Oxford region

Journal of medical genetics, 1984-08, Vol.21 (4), p.272-277

1984

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Long term effects of periconceptional multivitamin supplements for prevention of neural tube defects: a seven to 10 year follow up

Archives of disease in childhood, 1992-12, Vol.67 (12), p.1436-1441

1992

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DETECTION OF BREAKPOINTS IN SUBMICROSCOPIC CHROMOSOMAL TRANSLOCATION, ILLUSTRATING AN IMPORTANT MECHANISM FOR GENETIC DISEASE

The Lancet (British edition), 1989-10, Vol.334 (8667), p.819-824

1989

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Maternal serum alpha-fetoprotein measurement: a screening test for Down syndrome

The Lancet (British edition), 1984-04, Vol.1 (8383), p.926-929

1984

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Recurrence of neural tube defect in a group of at risk women: a 10 year study of Pregnavite Forte F

Journal of medical genetics, 1992-02, Vol.29 (2), p.134-135

1992

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Pulmonary agenesis as part of the VACTERL sequence

Archives of disease in childhood, 1988-07, Vol.63 (7 Spec No), p.723-726

1988

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Neocerebellar Hypoplasia in a Neonate Following Intra‐uterine Exposure to Anticonvulsants

Developmental medicine and child neurology, 1990-08, Vol.32 (8), p.737-742

1990

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The prevalence of translocations in parents of children with regular trisomy 21: a possible interchromosomal effect?

Journal of medical genetics, 1985-02, Vol.22 (1), p.24-28

1985

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Limb abnormalities and chorion villus sampling

The Lancet (British edition), 1991-07, Vol.338 (8758), p.51-51

1991

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Maternal 3;13 chromosome insertion, with severe pre-eclampsia

Clinical genetics, 1995-01, Vol.47 (1), p.17-21

1995

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Clinical features and molecular analysis of the α thalassemia/mental retardation syndromes. 1. Cases due to deletions involving chromosome band 16p13.3

American journal of human genetics, 1990-06, Vol.46 (6), p.1112-1126

1990

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Involvement of the mitogen-activated protein kinase cascade in peroxynitrite-mediated arachidonic acid release in vascular smooth muscle cells

American Journal of Physiology: Cell Physiology, 2004-06, Vol.286 (6), p.C1271-C1280

2004

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Paracentric inversions in man

Journal of medical genetics, 1984-12, Vol.21 (6), p.407-412

1984

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Predicting Huntington's disease

The Lancet (British edition), 1990-01, Vol.335 (8683), p.230-230

1990

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Pitted enamel hypoplasia in tuberous sclerosis patients and first-degree relatives

Clinical genetics, 1987-10, Vol.32 (4), p.216-221

1987

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Unfulfilled sterilization requests: what happens 6 months later?

Severe limb abnormalities after chorion villus sampling at 56-66 days' gestation

Physical mapping across the fragile X: Hypermethylation and clinical expression of the fragile X syndrome

Clinical features and molecular analysis of the α thalassemia/mental retardation syndromes. I, Cases due to deletions involving chromosome band 16p13.3

Molecular studies of trisomy 18

Clinical features and molecular analysis of the α thalassemia/mental retardation syndromes. II, Cases without detectable abnormality of the α globin complex

Unusual segregation of constitutional 11q;22q translocation may be explained by crossover in interchange segment, followed by 3 : 1 segregation at meiosis I

UK clinicians' knowledge of and attitudes to the prenatal diagnosis of single gene disorders

Parental decisions regarding termination of pregnancy following prenatal detection of sex chromosome abnormality

Prevalence of Huntington's disease among UK immigrants from the Indian subcontinent

Tuberous sclerosis: a new estimate of prevalence within the Oxford region

Long term effects of periconceptional multivitamin supplements for prevention of neural tube defects: a seven to 10 year follow up

DETECTION OF BREAKPOINTS IN SUBMICROSCOPIC CHROMOSOMAL TRANSLOCATION, ILLUSTRATING AN IMPORTANT MECHANISM FOR GENETIC DISEASE

Maternal serum alpha-fetoprotein measurement: a screening test for Down syndrome

Recurrence of neural tube defect in a group of at risk women: a 10 year study of Pregnavite Forte F

Pulmonary agenesis as part of the VACTERL sequence

Neocerebellar Hypoplasia in a Neonate Following Intra‐uterine Exposure to Anticonvulsants

The prevalence of translocations in parents of children with regular trisomy 21: a possible interchromosomal effect?

Limb abnormalities and chorion villus sampling

Maternal 3;13 chromosome insertion, with severe pre-eclampsia

Clinical features and molecular analysis of the α thalassemia/mental retardation syndromes. 1. Cases due to deletions involving chromosome band 16p13.3

Involvement of the mitogen-activated protein kinase cascade in peroxynitrite-mediated arachidonic acid release in vascular smooth muscle cells

Paracentric inversions in man

Predicting Huntington's disease

Pitted enamel hypoplasia in tuberous sclerosis patients and first-degree relatives

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