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Detailed screening for fetal anomalies and cardiac defects at the 11–13‐week scan

Ultrasound in obstetrics & gynecology, 2006-06, Vol.27 (6), p.613-618

2006

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Geographic dimensions of heat-related mortality in seven U.S. cities

Environmental research, 2015-04, Vol.138, p.439-452

2015

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Burnout syndrome in seafarers in the merchant marine service

International archives of occupational and environmental health, 2013-05, Vol.86 (4), p.407-416

2013

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Genomic chondrocyte culture profiling by array-CGH, interphase-FISH and RT-PCR

Osteoarthritis and cartilage, 2012-09, Vol.20 (9), p.1039-1045

2012

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The impact of first trimester screening and early fetal anomaly scan on invasive testing rates in women with advanced maternal age

Ultraschall in der Medizin, 2011-06, Vol.32 (3), p.302-306

2011

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Re-irradiation with Radiosurgery for Recurrent Glioblastoma Multiforme

Technology in cancer research & treatment, 2011-06, Vol.10 (3), p.253-258

2011

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Interphase M-FISH applications using commercial probes in prenatal and PGD diagnostics

Cytogenetic and genome research, 2006-08, Vol.114 (3-4), p.296-301

2006

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Dystocia and Fetotomy Associated with Cerebral Aplasia in a Greater One-horned Rhinoceros (Rhinoceros unicornis)

Reproduction in domestic animals, 2011-02, Vol.46 (1), p.e97-e101

2011

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First-Trimester Prenatal Diagnosis of Okihiro Syndrome

Fetal diagnosis and therapy, 2010-01, Vol.27 (4), p.222-226

2010

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A mixture model of nuchal translucency thickness in screening for chromosomal defects: validation of a single operator dataset

Prenatal diagnosis, 2010-11, Vol.30 (11), p.1100-1106

2010

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Prenatal diagnosis of familial absent pulmonary valve syndrome: case report and review of the literature

Ultrasound in obstetrics & gynecology, 2001-03, Vol.17 (3), p.263-267

2001

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Long-term radiographic and endocrinological outcomes of stereotactic radiosurgery for recurrent or residual nonfunctioning pituitary adenomas

Journal of neurosurgery, 2024-09, Vol.141 (3), p.773-8

2024

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Factor analysis of exercise capacity, dyspnoea ratings and lung function in patients with severe COPD

The European respiratory journal, 1994-04, Vol.7 (4), p.725-729

1994

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Family Quality of Life Following Early Identification of Deafness

Language, speech & hearing services in schools, 2010-04, Vol.41 (2), p.194-205

2010

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Plasma butyrylcholinesterase activity: a possible biomarker for differential diagnosis between Alzheimer's disease and dementia with Lewy bodies?

International journal of neuroscience, 2017-12, Vol.127 (12), p.1082-1086

2017

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10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences

Cytogenetic and genome research, 2009-01, Vol.124 (1), p.102-105

2009

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The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21

American journal of human genetics, 1997-03, Vol.60 (3), p.605-610

1997

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Clinical variability of Larsen syndrome: diagnosis in a father after sonographic detection of a severely affected fetus

Clinical genetics, 2000-02, Vol.57 (2), p.148-150

2000

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Forty-eight new cases with infertility due to balanced chromosomal rearrangements: Detailed molecular cytogenetic analysis of the 90 involved breakpoints

International journal of molecular medicine, 2007-06, Vol.19 (6), p.855-864

2007

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Epignathus: always a simple teratoma? Report of an exceptional case with two additional fetiforme bodies

Ultrasound in obstetrics & gynecology, 2003-04, Vol.21 (4), p.397-403

2003

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Effects of Theophylline Withdrawal in Severe Chronic Obstructive Pulmonary Disease

Chest, 1993-10, Vol.104 (4), p.1101-1107

1993

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Lung function, biological monitoring, and biological effect monitoring of gemstone cutters exposed to beryls

Occupational and environmental medicine (London, England), 2000-02, Vol.57 (2), p.133-139

2000

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DNA, FISH and complementation studies in ICF syndrome : DNA hypomethylation of repetitive and single copy loci and evidence for a trans acting factor

Human genetics, 1995-11, Vol.96 (5), p.562-571

1995

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The Fanconi Anemia Group E Gene, FANCE, Maps to Chromosome 6p

American journal of human genetics, 1999-05, Vol.64 (5), p.1400-1405

1999

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PARTIAL TRISOMY/MONOSOMY 6q IN FETAL CELLS AND CVS LONG-TERM CULTURE NOT PRESENT IN CVS SHORT-TERM CULTURE

Prenatal diagnosis, 1996-08, Vol.16 (8), p.741-748

1996

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Detailed screening for fetal anomalies and cardiac defects at the 11–13‐week scan

Geographic dimensions of heat-related mortality in seven U.S. cities

Burnout syndrome in seafarers in the merchant marine service

Genomic chondrocyte culture profiling by array-CGH, interphase-FISH and RT-PCR

The impact of first trimester screening and early fetal anomaly scan on invasive testing rates in women with advanced maternal age

Re-irradiation with Radiosurgery for Recurrent Glioblastoma Multiforme

Interphase M-FISH applications using commercial probes in prenatal and PGD diagnostics

Dystocia and Fetotomy Associated with Cerebral Aplasia in a Greater One-horned Rhinoceros (Rhinoceros unicornis)

First-Trimester Prenatal Diagnosis of Okihiro Syndrome

A mixture model of nuchal translucency thickness in screening for chromosomal defects: validation of a single operator dataset

Prenatal diagnosis of familial absent pulmonary valve syndrome: case report and review of the literature

Long-term radiographic and endocrinological outcomes of stereotactic radiosurgery for recurrent or residual nonfunctioning pituitary adenomas

Factor analysis of exercise capacity, dyspnoea ratings and lung function in patients with severe COPD

Family Quality of Life Following Early Identification of Deafness

Plasma butyrylcholinesterase activity: a possible biomarker for differential diagnosis between Alzheimer's disease and dementia with Lewy bodies?

10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences

The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21

Clinical variability of Larsen syndrome: diagnosis in a father after sonographic detection of a severely affected fetus

Forty-eight new cases with infertility due to balanced chromosomal rearrangements: Detailed molecular cytogenetic analysis of the 90 involved breakpoints

Epignathus: always a simple teratoma? Report of an exceptional case with two additional fetiforme bodies

Effects of Theophylline Withdrawal in Severe Chronic Obstructive Pulmonary Disease

Lung function, biological monitoring, and biological effect monitoring of gemstone cutters exposed to beryls

DNA, FISH and complementation studies in ICF syndrome : DNA hypomethylation of repetitive and single copy loci and evidence for a trans acting factor

The Fanconi Anemia Group E Gene, FANCE, Maps to Chromosome 6p

PARTIAL TRISOMY/MONOSOMY 6q IN FETAL CELLS AND CVS LONG-TERM CULTURE NOT PRESENT IN CVS SHORT-TERM CULTURE

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