Physician

Pediatrics

Dr. Celia I. Kaye, MD

Celia Kaye practices Pediatrics. Celia Kaye has written publications. She has 31 publications published with PubMed. The lastest publication is: 'Growth hormone insufficiency associated with haploinsufficiency at 18q23.'

Publications

University of Colorado Denver School of Medicine.
Assuring clinical genetic services for newborns identified through U.S. newborn screening programs.
Implementing a simpler approach to mission-based planning in a medical school.
Growth hormone benefits children with 18q deletions.
Folic acid awareness and use among women with a history of a neural tube defect pregnancy--Texas, 2000-2001.
Ganglioneuroblastoma and fetal hydantoin-alcohol syndromes.
Trisomy 8p: unusual origin detected by fluorescence in situ hybridization.
Progressive early dermatologic changes in Hutchinson-Gilford progeria syndrome.
Proximal 7q interstitial deletion in a severely mentally retarded and mildly abnormal infant.
Oculoauriculovertebral anomaly: segregation analysis.
Membranous nephropathy in two human leukocyte antigen-identical brothers.
Implementing screening for Lynch syndrome among patients with newly diagnosed colorectal cancer: summary of a public health/clinical collaborative meeting.
Measuring contributions to the research mission of medical schools.
What questions should newborn screening long-term follow-up be able to answer? A statement of the US Secretary for Health and Human Services' Advisory Committee on Her...
Rumination risk of aspiration of gastric contents in the Prader-Willi syndrome.
Genetics education for primary care providers in community health settings.
Magnetic resonance imaging demonstrates incomplete myelination in 18q- syndrome: evidence for myelin basic protein haploinsufficiency.
Short-limb dwarfism and hypertrophic cardiomyopathy in a patient with paternal isodisomy 14: 45,XY,idic(14)(p11).
A conference for the education of families who have a member with phenylketonuria.
Preferential loss of the paternal alleles in the 18q- syndrome.
Growth hormone insufficiency associated with haploinsufficiency at 18q23.
Integrating genetic services into public health--guidance for state and territorial programs from the National Newborn Screening and Genetics Resource Center (NNSGRC).
Growth hormone deficiency associated in the 18q deletion syndrome.
Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18q.
Introduction to the newborn screening fact sheets.
Newborn screening fact sheets.
Update of newborn screening and therapy for congenital hypothyroidism.
Perceptions of Mexican American clients receiving genetic services in South Texas.
Outcomes of interest in evidence-based evaluations of genetic tests.
Tracking clinical genetic services for newborns identified through newborn dried bloodspot screening in the United States-lessons learned.

Schools

Wayne State University

Doctors Specialties

Clinical Biochemical Genetics
Clinical Cytogenetics
Clinical Genetics
Pediatrics

Accepted Insurances

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