JeanetteCRamerMD

PubMed

• 3 citations
  Baraitser-Winter cerebrofrontofacial syndrome: Delineation of the spectrum in 42 cases
  Alain Verloes, Nataliya Di Donato, Julien Masliah-Planchon, Marjolijn C.J. Jongmans, Omar A Abdul-Raman, Beate Albrecht, Judith Allanson, Han G. Brunner, Débora Romeo ...> ;European Journal of Human Genetics. 2015 Mar 1
• 4 citations
  Malformations in a child with dup (7 pter‐p15.1) and del (7 q36‐qter) as a result of familial pericentric inversion
  Jeanette C. Ramer, Philip N. Mowrey, Roger L. Ladda> ;Clinical Genetics. 2008 Jun 28
• Absence of linkage of apparently single gene mediated ADHD with the human syntenic region of the mouse mutant coloboma
  Ellen J. Hess, Peter K. Rogan, Mark Domoto, Dorris E. Tinker, Roger L. Ladda, Jeanette C. Ramer> ;American Journal of Medical Genetics. 1995 Dec 18
• 1 citations
  Previously apparently undescribed syndrome: shallow orbits, ptosis, coloboma, trigonocephaly, gyral malformations, and mental and growth retardation.
  Ramer, J. C., Lin, A. E., Dobyns, W. B., Winter, R., Aymé, S., Pallotta, R., Ladda, R. L.> ;American journal of medical genetics. 1995 Jul 3
• Familial leuconychia, knuckle pads, hearing loss, and palmoplantar hyperkeratosis: an additional family with Bart-Pumphrey syndrome.
  Jeanette C. Ramer, David B. Vasily, Roger L. Ladda> ;Journal of Medical Genetics. 1994 Jan 1
• Congenital Contractures, Ectodermal Dysplasia, Cleft Lip/Palate, and Developmental Impairment: A Distinct Syndrome
  Roger L. Ladda, Jonathan Zonana, Jeanette C. Ramer, Maria J. Mascari, Peter K. Rogan> ;American Journal of Medical Genetics. 1993 Sep 15
• 9 citations
  Identical twins with Weissenbacher-Zweymüller syndrome and neural tube defect.
  Ramer, J. C., Eggli, K., Rogan, P. K., Ladda, R. L.> ;American journal of medical genetics. 1993 Mar 1
• Marden-Walker phenotype: Spectrum of variability in three infants
  Jeanette C. Ramer, Carl A. Frankel, Roger L. Ladda> ;American Journal of Medical Genetics. 1993 Feb 1
• 1 citations
  Cutaneous scar at anterior hair line in mother and child with associated frontal bone defect in child.
  John P. Stratis, Jeanette C. Ramer, Ernest K. Manders, Ralph A. W. Lehman, Roger L. Ladda> ;American Journal of Medical Genetics. 1992 Sep 15
• A Developmental Index Using the Wechsler Intelligence Scale for Children Implications for the Diagnosis and Nature of ADHD
  Thomas G. Bowers, Marcia G. Risser, John F. Suchanec, Dorris E. Tinker, Jeanette C. Ramer, Mark Domoto> ;Journal of Learning Disabilities. 1992 Mar 1
• 1 citations
  Melnick-Needles syndrome. Four new cases.
  Eggli, K., Giudici, M., Ramer, J., Easterbrook, J., Madewell, J.> ;Pediatric radiology. 1992 Jan 1
• 40 citations
  Five children with del (2)(q31q33) and one individual with dup (2)(q31q33) from a single family : review of brain, cardiac, and limb malformations
  Jeanette C. Ramer, Philip N. Mowrey, David B. Robins, Saverio Ligato, Javad Towfighi, Roger L. Ladda> ;American Journal of Medical Genetics. 1990 Nov 1
• 2 citations
  Humero-radial synostosis with ulnar defects in sibs.
  Jeanette C. Ramer, Roger L. Ladda> ;American Journal of Medical Genetics. 1989 Jun 1
• 8 citations
  Two infants with del(3)(p25pter) and a review of previously reported cases.
  Ramer, J. C., Ladda, R. L., Frankel, C.> ;American journal of medical genetics. 1989 May 1
• 26 citations
  A review of phenotype-karyotype correlations in individuals with interstitial deletions of the long arm of chromosome 2.
  Jeanette C. Ramer, Roger L. Ladda, Carl A. Frankel, Avril Beckford> ;American Journal of Medical Genetics. 1989 Mar 1
• Multiple pterygium syndrome. An overview.
  Jeanette C. Ramer, Roger L. Ladda, William W. Demuth> ;JAMA Pediatrics. 1988 Jul 1
• 2 citations
  Magnetic resonance imaging in leukodystrophies of childhood.
  Young, R. S., Osbakken, M. D., Alger, P. M., Ramer, J. C., Weidner, W. A., Daigh, J. D.> ;Pediatric neurology. 1985 Jan 1
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