Jessica G. Davis

发表

Insurance reimbursement for risk-reducing mastectomy and oophorectomy in women with BRCA1 or BRCA2 mutations

K. Offit, R. Barakat, M. Robson, 2001, Genetics in Medicine.

Cancer genetic testing and assisted reproduction.

K. Offit, S. Cummings, K. Kohut, 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Predictive Genetic Tests: Problems and Pitfalls

Jessica G. Davis, 1997, Annals of the New York Academy of Sciences.

Decisions about Reproduction: Genetic Counseling

Jessica G. Davis, 1978 .

Assessment of bone mineral density in adults and children with Marfan syndrome

P. Giampietro, M. Peterson, O. Boachie-Adjei, 2003, Osteoporosis International.

Marfan syndrome: orthopedic and genetic review

P. Giampietro, Jessica G. Davis, C. Raggio, 2002, Current opinion in pediatrics.

Interleukin 1 receptor antagonist deficiency presenting as infantile pustulosis mimicking infantile pustular psoriasis.

R. Goldbach-Mansky, C. Magro, Kira Minkis, 2012, Archives of dermatology.

Cytogenetic findings in the dysmyelopoietic syndrome

D. Budman, V. Vinciguerra, Jessica G. Davis, 1982, Cancer.

Characterization of a novel receptor mutation A-->T at exon 4 in complete androgen insensitivity syndrome and a carrier sibling via bidirectional polymorphism sequence analysis.

M. Tucker, M. Perloe, Jessica G. Davis, 2002, International journal of molecular medicine.

The Kathryn O. and Alan C. Greenberg Center for Skeletal Dysplasias: An Interdisciplinary Approach

Jessica G. Davis, Erin M. Carter, C. Raggio, 2008, HSS Journal.

Advances in understanding etiology of achondroplasia and review of management

Jessica G. Davis, Erin M. Carter, C. Raggio, 2007, Current opinion in pediatrics.

Evaluation of Growth and Hormonal Status in Patients Referred to the International Fanconi Anemia Registry

S. Batish, A. Auerbach, M. New, 2001, Pediatrics.

Prenatal diagnosis of trisomy 3 mosaicism

D. Blumenthal, Jessica G. Davis, A. Zaslav, 2004, Prenatal diagnosis.

Prenatal diagnosis of trisomy 20 mosaicism

E. Lieber, Jessica G. Davis, L. Hsu, 1979, Clinical genetics.

Ethnically diverse causes of Walker‐Warburg syndrome (WWS): FCMD mutations are a more common cause of WWS outside of the Middle East

C. Walsh, W. Dobyns, Karen R Schmidt, 2008, Human mutation.

Congenital fusion of the fourth and fifth metacarpals associated with primary gonadal failure

P. Giampietro, M. Harbison, P. Brill, 1996, Skeletal Radiology.

Partial deletion o/the short arm of chromosome No 4(4t,-). Clinical ,t,di , i, unrelated patients

H. Klinger, W. R. Breg, D. Warburton, 1970 .

Prenatal Genetic Services: Toward a National Data Base

F. Meaney, Jessica G. Davis, S. Riggle, 1993, Clinical obstetrics and gynecology.

The Incidence of Protrusio Acetabuli in Marfan's Syndrome and Its Relationship to Bone Mineral Density

P. Giampietro, O. Boachie-Adjei, S. Burke, 2000, Journal of pediatric orthopedics.

Marfan Syndrome in Adolescents and Young Adults: Psychosocial Functioning and Knowledge

S. B. Friedman, S. Friedman, M. Fisher, 1990, Journal of developmental and behavioral pediatrics : JDBP.

Further phenotypic delineation of subtelomeric (terminal) 4q deletion with emphasis on intracranial and reproductive anatomy

Eric Scott Sills, P. Papenhausen, Peter R Papenhausen, 2007, Orphanet journal of rare diseases.

Chromosomal mosaicism in amniotic fluid cell cultures.

E. Jenkins, Jessica G. Davis, N. Kardon, 1977, The Journal of pediatrics.

Enhancing patient autonomy with risk assessment and invasive diagnosis: an ethical solution to a clinical challenge.

F. Chervenak, L. Mccullough, S. Gross, 2008, American journal of obstetrics and gynecology.

Diagnosis of Fanconi anemia in patients without congenital malformations: an international Fanconi Anemia Registry Study.

P. Giampietro, A. Auerbach, P. Verlander, 1997, American journal of medical genetics.

FANCONI ANEMIA: A MODEL FOR GENETIC CAUSES OF ABNORMAL BRAIN DEVELOPMENT

P. Giampietro, S. Pavlakis, A. Auerbach, 1992, Developmental medicine and child neurology.

Phenotypic features and impact of beta blocker or calcium antagonist therapy on aortic lumen size in the Marfan syndrome.

M. Roman, K. Ehlers, Jessica G. Davis, 1999, The American journal of cardiology.

Bone Mineral Density Determinations by Dual-Energy x-ray Absorptiometry in the Management of Patients with Marfan Syndrome—Some Factors Which Affect the Measurement

P. Giampietro, M. Peterson, O. Boachie-Adjei, 2007, HSS Journal.