Clinical Assistant Professor, Pediatrics, University of Maryland School of Medicine
Pediatrics
Dr. Antonie D. Kline, MD
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Doctor Antonie D. Kline, MD works in the field of Pediatrics. She graduated from Jefferson Medical College. She received awards:"Fellow (FAAP)". Antonie D. Kline, MD has written publications. She has 19 publications published with PubMed. The lastest publication is: 'Mandibulofacial Dysostosis with Microcephaly: Mutation and Database Update.' Antonie Kline accepts Medicare.
Publications
- Mandibulofacial Dysostosis with Microcephaly: Mutation and Database Update.
- Autism traits in children and adolescents with Cornelia de Lange syndrome.
- Cornelia de Lange syndrome: Further delineation of phenotype, cohesin biology and educational focus, 5th Biennial Scientific and Educational Symposium abstracts.
- Newborn screening for X-linked adrenoleukodystrophy: Further evidence high throughput screening is feasible.
- Causes of death and autopsy findings in a large study cohort of individuals with Cornelia de Lange syndrome and review of the literature.
- Facial diagnosis of mild and variant CdLS: Insights from a dysmorphologist survey.
- Cornelia de Lange syndrome: extending the physical and psychological phenotype.
- SMC1A expression and mechanism of pathogenicity in probands with X-Linked Cornelia de Lange syndrome.
- Natural history of aging in Cornelia de Lange syndrome.
- Cornelia de Lange syndrome: clinical review, diagnostic and scoring systems, and anticipatory guidance.
- Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation.
- NIPBL mutational analysis in 120 individuals with Cornelia de Lange syndrome and evaluation of genotype-phenotype correlations.
- A de novo complex karyotype with two independent balanced translocations and a double inversion of chromosome 6 presenting with multiple congenital anomalies.
- Isolated NIPBL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction.
- Isolated NIBPL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction.
- Genome-wide DNA methylation analysis in cohesin mutant human cell lines.
- Characterization of sleep disturbance in Cornelia de Lange Syndrome.
- Genotype-phenotype correlation in CC2D2A-related Joubert syndrome reveals an association with ventriculomegaly and seizures.
Schools
Thomas Jefferson University
Sinai Hospital Of Baltimore
Jefferson Med College
Johns Hopkins University
Doctors Specialties
- Clinical Cytogenetics
- Clinical Genetics
- Clinical Molecular Genetics
- Pediatrics
Accepted Insurances
Awards
- Fellow (FAAP)
Education
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Sinai Hospital of Baltimore -
Jefferson Medical College
Hospital
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University of Maryland Medical Center
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1154347425 |
| Last Name Of The Provider | KLINE |
| First Name Of The Provider | ANTONIE |
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