J. Ramer

发表

Two infants with del(3)(p25pter) and a review of previously reported cases.

R. Ladda, C. Frankel, J. Ramer, 1989, American journal of medical genetics.

Absence of linkage of apparently single gene mediated ADHD with the human syntenic region of the mouse mutant Coloboma.

P. Rogan, E. Hess, R. Ladda, 1995, American journal of medical genetics.

Static encephalopathies of infancy and childhood

G. Miller, J. Ramer, 1992 .

Five children with del (2)(q31q33) and one individual with dup (2)(q31q33) from a single family: review of brain, cardiac, and limb malformations.

J. Towfighi, R. Ladda, J. Ramer, 1990, American journal of medical genetics.

A review of phenotype-karyotype correlations in individuals with interstitial deletions of the long arm of chromosome 2.

R. Ladda, C. Frankel, J. Ramer, 1989, American journal of medical genetics.

Alexander's disease: Further light-, and electron-microscopic observations

J. Towfighi, D. Horoupian, J. Sassani, 2004, Acta Neuropathologica.

Identical twins with Weissenbacher-Zweymüller syndrome and neural tube defect.

P. Rogan, R. Ladda, K. Eggli, 1993, American journal of medical genetics.

Outcome After Open-Heart Surgery in Infants and Children

J. Tesman, G. Miller, J. Myers, 1996, Journal of child neurology.

Marden-Walker phenotype: spectrum of variability in three infants.

R. Ladda, C. Frankel, J. Ramer, 1993, American journal of medical genetics.

Familial leuconychia, knuckle pads, hearing loss, and palmoplantar hyperkeratosis: an additional family with Bart-Pumphrey syndrome.

R. Ladda, D. Vasily, J. Ramer, 1994, Journal of medical genetics.

Prolonged low flow isoflurane anesthesia for status epilepticus.

M. Snider, W. Kofke, R. Young, 1985, Anesthesiology.

Multiple pterygium syndrome. An overview.

R. Ladda, J. Ramer, W. Demuth, 1988, American journal of diseases of children.

Phenotypic variation of multiple pterygium syndrome in siblings, including identical twins

R. Ladda, J. Ramer, E. Kilchevsky, 1991 .

Anorexia nervosa: staff subversion of therapy.

J. Ramer, D. E. Tinker, 1983, Journal of adolescent health care : official publication of the Society for Adolescent Medicine.

Magnetic resonance imaging in leukodystrophies of childhood.

M. Osbakken, W. Weidner, J. D. Daigh, 1985, Pediatric neurology.

Malformations in a child with dup (7 pter‐p15.1) and del (7 q36‐qter) as a result of familial pericentric inversion

R. Ladda, J. Ramer, P. Mowrey, 1991, Clinical genetics.

Adrenoleukodystrophy: Unusual Computed Tomographic Appearance

H. Moser, R. Lehman, J. Towfighi, 1982 .

Baraitser–Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases

B. V. van Bon, A. Hoischen, K. Devriendt, 2014, European Journal of Human Genetics.

Previously apparently undescribed syndrome: shallow orbits, ptosis, coloboma, trigonocephaly, gyral malformations, and mental and growth retardation.

R. Winter, W. Dobyns, A. Lin, 1995, American journal of medical genetics.

ESTIMATING WAIS IQ FROM SHIPLEY SCALE SCORES: ANOTHER CROSS-VALIDATION.

L. A. Stone, L A STONE, J C RAMER, 1965, Journal of clinical psychology.

Congenital contractures, ectodermal dysplasia, cleft lip/palate, and developmental impairment: a distinct syndrome.

P. Rogan, J. Zonana, R. Ladda, 1993, American journal of medical genetics.

Humero-radial synostosis with ulnar defects in sibs.

R. Ladda, J. Ramer, 1989, American journal of medical genetics.

Cholesterol, GM1, and Autism

F. Ali-Rahmani, C. Schengrund, J. Ramer, 2012, Neurochemical Research.

Short-term admission for behavior modification.

J. Ramer, M. Domoto, D. E. Tinker, 1986, American journal of diseases of children.

Syndrome identification #149: Trigonocephaly, pachygyria, retinal coloboma, and cardiac defect: A distinct syndrome

R. Ladda, E. Manders, J. Ramer, 1992 .