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| Educational background |
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M.D., Pennsylvania State University College of Medicine, 1977
Residency, Penn State Milton S. Hershey Medical Center
Fellowship, Penn State Milton S. Hershey Medical Center
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| Areas of expertise |
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| Leukodystrophy, Metachromatic | Frontal Bone |
| Chromosome Aberrations | Radius |
| Inversion, Chromosome | Keratosis |
| Mental Retardation | Chromosomes, Human, Pair 2 |
| Brain | Twins, Monozygotic |
| Cicatrix | Diffuse Cerebral Sclerosis of Schilder |
| Limb Deformities, Congenital | Multigene Family |
| Osteochondrodysplasias | Synostosis |
| Chromosome Deletion | Ectodermal Dysplasia |
| Ulna | Humerus |
| Chromosomes, Human, Pair 3 | Diseases in Twins |
| Chromosomes, Human, Pair 7 | Neural Tube Defects |
| Magnetic Resonance Imaging | Mice, Mutant Strains |
| Blepharophimosis | Attention Deficit Disorder with Hyperactivity |
| Pterygium | Hearing Disorders |
| Heart Defects, Congenital | Abnormalities, Multiple |
| Scalp | Wechsler Scales |
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| Publication author name |
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| Select publications |
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Ladda RL. Zonana J. Ramer JC. Mascari MJ. Rogan PK. Congenital contractures, ectodermal dysplasia, cleft lip/palate, and developmental impairment: a distinct syndrome. 1993 Sep 15. Am J Med Genet. 47(4):550-5.
National Institute of Arthritis and Musculoskeletal and Skin Diseases
Ramer JC. Vasily DB. Ladda RL. Familial leuconychia, knuckle pads, hearing loss, and palmoplantar hyperkeratosis: an additional family with Bart-Pumphrey syndrome. 1994 Jan. J Med Genet. 31(1):68-71.
Hess EJ. Rogan PK. Domoto M. Tinker DE. Ladda RL. Ramer JC. Absence of linkage of apparently single gene mediated ADHD with the human syntenic region of the mouse mutant Coloboma. 1995 Dec 18. Am J Med Genet. 60(6):573-9.
National Center for Research Resources
National Institute of Child Health and Human Development
Ramer JC. Lin AE. Dobyns WB. Winter R. Aymé S. Pallotta R. Ladda RL. Previously apparently undescribed syndrome: shallow orbits, ptosis, coloboma, trigonocephaly, gyral malformations, and mental and growth retardation. 1995 Jul 3. Am J Med Genet. 57(3):403-9.
Eggli K. Giudici M. Ramer J. Easterbrook J. Madewell J. Melnick-Needles syndrome. Four new cases. 1992. Pediatr Radiol. 22(4):257-61.
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