J. Davis

发表

Counseling parents after the birth of an infant with Down's syndrome.

D. Golden, J. Davis, 1974, Children today.

Chromosomal mosaicism in amniotic fluid cell cultures.

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

Factors influencing mammalian X chromosome condensation and sex chromatin formation. I. The effect of in vitro cell density on sex chromatin frequency.

H. Klinger, J. Davis, P. Goldhuber, 1968, Cytogenetics.

Partial deletion of the short arm of chromosome no. 4(4p-): clinical studies in five unrelated patients.

D. Miller, H. Klinger, W. R. Breg, 1970, The Journal of pediatrics.

The 13q-deletion syndrome.

D. Miller, H. Klinger, O. Miller, 1969, American journal of human genetics.

A child with presumptive monosomy 21 (45,XY,-21) in a family in which some members are Gq-.

H. Klinger, E. Jenkins, J. Davis, 1976, Cytogenetics and cell genetics.

The roentgen findings in gastric leiomyomas and leiomyosarcomas.

D. Adams, J. Davis, 1956, Radiology.

Retroperitoneal mucocele of the appendix; a case report with characteristic roentgen features.

L. J. Bonann, J. Davis, 1948, Radiology.

Definition of the critical interval for Smith-Magenis syndrome.

P. Patel, B. Finucane, R. Magenis, 1997, Cytogenetics and cell genetics.

The need for more accurate and timely diagnosis in Fanconi anemia: a report from the International Fanconi Anemia Registry.

P. Giampietro, S. Pavlakis, A. Auerbach, 1993, Pediatrics.

A pediatrician's approach to counseling families of mentally retarded children.

J. Davis, 1973, Pediatric annals.

Radiation exposure and associated risks to operating-room personnel during use of fluoroscopic guidance for selected orthopaedic surgical procedures.

M. Davis, J G Davis, M L Davis, 1983, The Journal of bone and joint surgery. American volume.

Erratum to the report of the third international workshop on human Y chromosome mapping 1997

A. Uitterlinden, E. Mullaart, A. Protopopov, 1997 .

Mediastinal carinal bronchogenic cysts.

J. Simonton, J. Davis, 1956, Radiology.

Neonatal alloimmune thrombocytopenia due to anti‐HPA‐5b (Bra, Zava, Hca): the importance of third‐generation platelet antibody detection techniques, a case report

R. Bell, C. Entwistle, J. Davis, 1992, Transfusion medicine.

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.

Use of the ultrasound aspiration transducer in midtrimester amniocentesis.

M. Goldman, N. Kardon, A. Fenton, 1984, The Journal of reproductive medicine.

PRE‐TRANSFUSION NON‐INVASIVE QUALITY ASSESSMENT OF STORED PLATELET CONCENTRATES

P. Mintz, E. Bellhouse, J. Davis, 1987, British journal of haematology.

A second case of neonatal alloimmune thrombocytopenia associated with anti-PlA2 (Zwb) antibodies.

Davis Jg, A. Gronkowska, G. Lucas, 1989, Haematologia.

The osseous radiographic findings of chronic renal insufficiency.

J. Davis, 1953, Radiology.

Thrombocytopenia in malaria.

N. White, S. Looareesuwan, D. Allen, 1992, The Southeast Asian journal of tropical medicine and public health.

De novo duplication of the 7q11 leads to q22 region.

N. Kardon, L. Pollack, A. Broekman, 1983, Journal of medical genetics.

Berry aneurysms, cirrhosis, pulmonary emphysema, and bilateral symmetrical cerebral calcifications: a new syndrome.

J. Markowitz, F. Daum, K. Kenigsberg, 1987, American journal of medical genetics. Supplement.

Interstitial deletion of chromosome 2 (p23p25).

R. Wapnir, V. Penchaszadeh, J. Davis, 1987, American journal of medical genetics.

A liveborn case of 49,XXXY, + 18.

E. Jenkins, M. Elice, N. Kardon, 1980, Journal of medical genetics.

New recessive syndrome characterized by increased chromosomal breakage and several findings which overlap with Fanconi anemia.

P. Giampietro, A. Auerbach, E. Elias, 1998, American journal of medical genetics.

Statement from the National Institutes of Health workshop on population screening for the cystic fibrosis gene.

K. Klinger, N. Holtzman, F. Collins, 1990, The New England journal of medicine.