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| Educational background |
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M.D., University of Chicago Pritzker School of Medicine, 1963
Internship, Children's Orthopaedic Hospital, Seattle
Residency, Children's Hospital of Boston
Fellowship, Massachusetts General Hospital
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| Areas of expertise |
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| Arginine | Ectromelia |
| Idoxuridine | Frontal Bone |
| Myocardium | Glioma |
| Muscular Dystrophies | Chromosomes, Human, Pair 15 |
| Chromosome Aberrations | Radius |
| Inversion, Chromosome | Chromosomes, Human, Pair 18 |
| Hemophilia A | Point Mutation |
| Keratosis | Dimethyl Sulfoxide |
| Prader-Willi Syndrome | Mental Retardation |
| Chromosomes, Human, Pair 2 | Eye Abnormalities |
| Glutamine | Hydrocephalus |
| Kidney | Brain |
| Face | Hydronephrosis |
| Central Nervous System | Dandy-Walker Syndrome |
| Twins, Monozygotic | Ellis-Van Creveld Syndrome |
| Cicatrix | Limb Deformities, Congenital |
| Osteochondrodysplasias | Multigene Family |
| Ectodermal Dysplasia | Synostosis |
| Chromosome Deletion | Ulna |
| Chromosomes, Human, Pair 21 | Humerus |
| Myosins | Cardiomyopathy, Hypertrophic |
| Chromosomes, Human, Pair 3 | Diseases in Twins |
| Chromosomes, Human, Pair 7 | Neural Tube Defects |
| X Chromosome | Down Syndrome |
| Microcephaly | Mice, Mutant Strains |
| Blepharophimosis | Retinitis Pigmentosa |
| Attention Deficit Disorder with Hyperactivity | Hearing Disorders |
| Pterygium | DNA |
| Scalp | Abnormalities, Multiple |
| Heart Defects, Congenital | Leukemia, Monocytic, Acute |
| Linkage (Genetics) | Precursor Cell Lymphoblastic Leukemia-Lymphoma |
| Factor VIII | |
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| Publication author name |
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| Select publications |
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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.
Consevage MW. Salada GC. Baylen BG. Ladda RL. Rogan PK. A new missense mutation, Arg719Gln, in the beta-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy. 1994 Jun. Hum Mol Genet. 3(6):1025-6.
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.
Rogan PK. Close P. Blouin JL. Seip JR. Gannutz L. Ladda RL. Antonarakis SE. Duplication and loss of chromosome 21 in two children with Down syndrome and acute leukemia. 1995 Nov 6. Am J Med Genet. 59(2):174-81.
National Human Genome Research Institute
National Institute of Child Health and Human Development
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