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A39 AUTOIMMUNE LUNG DISEASE: CASE REPORTS: Primary Sjogrens Syndrome Causing Pleural Effusions

American journal of respiratory and critical care medicine, 2017-01, Vol.195

2017

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C42 DYSPNEA: CASE REPORTS: Diaphragmatic Rupture Into The Lung In Patient With Muscular Dystrophy

American journal of respiratory and critical care medicine, 2017-01, Vol.195

2017

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C42 DYSPNEA: CASE REPORTS: A Case Report Of Pancreaticopleural Fistula In A Patient With Chronic Autoimmune Pancreatitis

American journal of respiratory and critical care medicine, 2017-01, Vol.195

2017

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C70 CALL MY NAME: CASE REPORTS IN PULMONARY VASCULAR DISEASE: Pulmonary Arterial Hypertension And Acute Respiratory Distress Syndrome In A Patient With Adult-Onset Stills Disease

American journal of respiratory and critical care medicine, 2017-01, Vol.195

2017

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The predictive value of findings of the common aneuploidies, trisomies 13, 18 and 21, and numerical sex chromosome abnormalities at CVS: experience from the ACC U.K. collaborative study

Prenatal diagnosis, 1999-09, Vol.19 (9), p.817-826

1999

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Effects of Lacrimal drainage occlusion with nondissolvable intracanalicular Plugs on hydrogel contact lens wear

Optometry and vision science, 1998-05, Vol.75 (5), p.330-338

1998

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Specific cytogenetic abnormalities are associated with a significantly inferior outcome in children and adolescents with mature B-cell non-Hodgkin's lymphoma: results of the FAB LMB 96 international study

Leukemia, 2009-02, Vol.23 (2), p.323-331

2009

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Two years' prospective experience using fluorescence in situ hybridization on uncultured amniotic fluid cells for rapid prenatal diagnosis of common chromosomal aneuploidies

Prenatal diagnosis, 1999-06, Vol.19 (6), p.546-551

1999

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Long-term culture of primary breast cancer in defined medium

Breast cancer research and treatment, 1996-01, Vol.39 (3), p.247-259

1996

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Trends in prenatal diagnosis of Down syndrome and other autosomal trisomies in Scotland 1990 to 1994, with associated cytogenetic and epidemiological findings

Genetic epidemiology, 1999, Vol.16 (2), p.179-190

1999

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Congenital ocular defects associated with an abnormality of the human chromosome 1: trisomy 1q32-qter

Journal of pediatric ophthalmology and strabismus, 1994-01, Vol.31 (1), p.41-45

1994

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Time flies

International contact lens clinic (1987), 1999-11, Vol.26 (6), p.146-146

1999

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Further consolidation of the contact lens industry? Maybe, maybe not

International contact lens clinic (1987), 1999-09, Vol.26 (5), p.110-110

Lowther, Gerald E.

1999

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Molecular cytogenetic characterization of a critical region in bands 7q35-q36 commonly deleted in malignant myeloid disorders

Blood, 1998-12, Vol.92 (11), p.4031-4035

1998

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Uniparental isodisomy for chromosome 16 in a growth-retarded infant with congenital heart disease

Prenatal diagnosis, 1995-06, Vol.15 (6), p.579-584

1995

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Prenatal Diagnosis in the United Kingdom - An Overview

European journal of human genetics : EJHG, 1997-01, Vol.5 (Suppl 1), p.84-89

1997

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Molecular Cytogenetic Characterization of a Critical Region in Bands 7q35-q36 Commonly Deleted in Malignant Myeloid Disorders

Blood, 1998-12, Vol.92 (11), p.4031-4035

1998

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A note on Hvorslev's intake factors

Géotechnique, 1978-12, Vol.28 (4), p.465-466

Lowther, G.

1978

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A case with Waardenburg syndrome presenting with two separate translocations--one reciprocal and one complex

Clinical dysmorphology, 2001-01, Vol.10 (1), p.65-66

2001

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A synopsis of extended-wear lenses and lens care regimens

Optometry clinics : the official publication of the Prentice Society, 1991, Vol.1 (3), p.63

Lowther, G E

1991

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Second-trimester placental biopsy for rapid fetal karyotyping

American journal of obstetrics and gynecology, 1990-09, Vol.163 (3), p.931-934

1990

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Prenatal diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiency

Prenatal diagnosis, 1987-02, Vol.7 (2), p.135-141

1987

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Fitting hydrogel bifocal contact lenses

Optometry clinics : the official publication of the Prentice Society, 1994, Vol.4 (1), p.121

1994

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No calculations required

Journal of the American Optometric Association, 1997-04, Vol.68 (4), p.214, 270

Lowther, G E

1997

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Cells collected from the corneal surface in Sjögren's syndrome, dry eye, and normals

Advances in experimental medicine and biology, 2002, Vol.506 (Pt B), p.925

2002

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A39 AUTOIMMUNE LUNG DISEASE: CASE REPORTS: Primary Sjogrens Syndrome Causing Pleural Effusions

C42 DYSPNEA: CASE REPORTS: Diaphragmatic Rupture Into The Lung In Patient With Muscular Dystrophy

C42 DYSPNEA: CASE REPORTS: A Case Report Of Pancreaticopleural Fistula In A Patient With Chronic Autoimmune Pancreatitis

C70 CALL MY NAME: CASE REPORTS IN PULMONARY VASCULAR DISEASE: Pulmonary Arterial Hypertension And Acute Respiratory Distress Syndrome In A Patient With Adult-Onset Stills Disease

The predictive value of findings of the common aneuploidies, trisomies 13, 18 and 21, and numerical sex chromosome abnormalities at CVS: experience from the ACC U.K. collaborative study

Effects of Lacrimal drainage occlusion with nondissolvable intracanalicular Plugs on hydrogel contact lens wear

Specific cytogenetic abnormalities are associated with a significantly inferior outcome in children and adolescents with mature B-cell non-Hodgkin's lymphoma: results of the FAB LMB 96 international study

Two years' prospective experience using fluorescence in situ hybridization on uncultured amniotic fluid cells for rapid prenatal diagnosis of common chromosomal aneuploidies

Long-term culture of primary breast cancer in defined medium

Trends in prenatal diagnosis of Down syndrome and other autosomal trisomies in Scotland 1990 to 1994, with associated cytogenetic and epidemiological findings

Congenital ocular defects associated with an abnormality of the human chromosome 1: trisomy 1q32-qter

Time flies

Further consolidation of the contact lens industry? Maybe, maybe not

Molecular cytogenetic characterization of a critical region in bands 7q35-q36 commonly deleted in malignant myeloid disorders

Uniparental isodisomy for chromosome 16 in a growth-retarded infant with congenital heart disease

Prenatal Diagnosis in the United Kingdom - An Overview

Molecular Cytogenetic Characterization of a Critical Region in Bands 7q35-q36 Commonly Deleted in Malignant Myeloid Disorders

A note on Hvorslev's intake factors

A case with Waardenburg syndrome presenting with two separate translocations--one reciprocal and one complex

A synopsis of extended-wear lenses and lens care regimens

Second-trimester placental biopsy for rapid fetal karyotyping

Prenatal diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiency

Fitting hydrogel bifocal contact lenses

No calculations required

Cells collected from the corneal surface in Sjögren's syndrome, dry eye, and normals

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