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Prenatal Bowel Findings in Male Siblings With a Confirmed FOXP3 Mutation

Journal of ultrasound in medicine, 2018-04, Vol.37 (4), p.1033-1037

2018

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Reproductive endocrinologists' utilization of genetic counselors and their services: is there an unmet need?

Fertility and sterility, 2019-09, Vol.112 (3), p.e352-e352

2019

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Prenatal Bowel Findings in Male Siblings With a Confirmed FOXP3 Mutation

Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine, 2018, Vol.37 (4), p.1033-1037

2018

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Molecular Genetics of Neurofibromatosis 2 and Related Tumors (Acoustic Neuroma and Meningioma)

Annals of the New York Academy of Sciences, 1991-04, Vol.615 (1), p.338-343

1991

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Parental origin of chromosome 22 loss in sporadic and NF2 neuromas

Genomics (San Diego, Calif.), 1991-05, Vol.10 (1), p.280-283

1991

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Equal parental origin of chromosome 22 losses in human sporadic meningioma : no evidence for genomic imprinting

American journal of human genetics, 1990-11, Vol.47 (5), p.823-827

1990

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Lethal osteosclerotic osteochondrodysplasia with platyspondyly, metaphyseal widening, and intracellular inclusions in sibs

American journal of medical genetics, 1998-12, Vol.80 (4), p.423-428

1998

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Standardized EEG interpretation accurately predicts prognosis after cardiac arrest

Neurology, 2016-04, Vol.86 (16), p.1482-1490

2016

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Multisite medical record review of emergency department visits for unspecified injury of head following the ICD-10-CM coding transition

Injury prevention, 2021-03, Vol.27 (Suppl 1), p.i13-i18

2021

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Hydrolysis of a series of parabens by skin microsomes and cytosol from human and minipigs and in whole skin in short-term culture

Toxicology and applied pharmacology, 2007-12, Vol.225 (2), p.221-228

2007

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Interventional Strategies for Children with Progressive Pulmonary Hypertension Despite Optimal Therapy. An Official American Thoracic Society Clinical Practice Guideline

American journal of respiratory and critical care medicine, 2024-11

2024

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Multisite medical record review of emergency department visits for traumatic brain injury

Injury prevention, 2021-03, Vol.27 (Suppl 1), p.i42-i48

2021

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Conserved CTL epitopes on the adenovirus hexon protein expand subgroup cross-reactive and subgroup-specific CD8+ T cells

Blood, 2004-10, Vol.104 (8), p.2432-2440

2004

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Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

Nature (London), 2010-04, Vol.464 (7289), p.713-720

2010

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Cancer and Leukemia Group B Pathology Committee Guidelines for Tissue Microarray Construction Representing Multicenter Prospective Clinical Trial Tissues

Journal of clinical oncology, 2011-06, Vol.29 (16), p.2282-2290

2011

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Auditory development in the absence of hearing in infancy

Neuroreport, 2010-02, Vol.21 (3), p.163-167

2010

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The distribution of esterases in the skin of the minipig

Toxicology letters, 2007-09, Vol.173 (2), p.118-123

2007

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Differential regulation of ACE2 gene expression in the heart and kidney of normotensive rats

American journal of hypertension, 2005-05, Vol.18 (5), p.A129-A130

2005

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To the editor

Journal of pediatric surgery, 2000-11, Vol.35 (11), p.1684

2000

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To the editor

Journal of pediatric surgery, 2000-11, Vol.35 (11), p.1684-1684

2000

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Localization of one gene for tuberous sclerosis within 9q32-9q34, and further evidence for heterogeneity

American journal of human genetics, 1991-10, Vol.49 (4), p.764-772

1991

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Crucial bronchoscopic findings in esophageal atresia and tracheoesophageal fistula

Journal of pediatric surgery, 1988-05, Vol.23 (5), p.466-470

1988

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Biomarker and cytologic abnormalities in women at high and low risk for breast cancer

Journal of cellular biochemistry, 1993, Vol.53 (S17G), p.153-160

1993

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A technique for preservation of the ileocecal valve in the neonatal short intestine

Journal of pediatric surgery, 1989-04, Vol.24 (4), p.369-370

1989

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Balloon catheter dilatation of focal intestinal strictures following necrotizing enterocolitis

Journal of pediatric surgery, 1985-12, Vol.20 (6), p.637-639

1985

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Prenatal Bowel Findings in Male Siblings With a Confirmed FOXP3 Mutation

Reproductive endocrinologists' utilization of genetic counselors and their services: is there an unmet need?

Prenatal Bowel Findings in Male Siblings With a Confirmed FOXP3 Mutation

Molecular Genetics of Neurofibromatosis 2 and Related Tumors (Acoustic Neuroma and Meningioma)

Parental origin of chromosome 22 loss in sporadic and NF2 neuromas

Equal parental origin of chromosome 22 losses in human sporadic meningioma : no evidence for genomic imprinting

Lethal osteosclerotic osteochondrodysplasia with platyspondyly, metaphyseal widening, and intracellular inclusions in sibs

Standardized EEG interpretation accurately predicts prognosis after cardiac arrest

Multisite medical record review of emergency department visits for unspecified injury of head following the ICD-10-CM coding transition

Hydrolysis of a series of parabens by skin microsomes and cytosol from human and minipigs and in whole skin in short-term culture

Interventional Strategies for Children with Progressive Pulmonary Hypertension Despite Optimal Therapy. An Official American Thoracic Society Clinical Practice Guideline

Multisite medical record review of emergency department visits for traumatic brain injury

Conserved CTL epitopes on the adenovirus hexon protein expand subgroup cross-reactive and subgroup-specific CD8+ T cells

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

Cancer and Leukemia Group B Pathology Committee Guidelines for Tissue Microarray Construction Representing Multicenter Prospective Clinical Trial Tissues

Auditory development in the absence of hearing in infancy

The distribution of esterases in the skin of the minipig

Differential regulation of ACE2 gene expression in the heart and kidney of normotensive rats

To the editor

To the editor

Localization of one gene for tuberous sclerosis within 9q32-9q34, and further evidence for heterogeneity

Crucial bronchoscopic findings in esophageal atresia and tracheoesophageal fistula

Biomarker and cytologic abnormalities in women at high and low risk for breast cancer

A technique for preservation of the ileocecal valve in the neonatal short intestine

Balloon catheter dilatation of focal intestinal strictures following necrotizing enterocolitis

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