J. McCombs

发表

cDNA sequence, interspecies comparison, and gene mapping analysis of argininosuccinate lyase.

S. Naylor, J. McGill, C. Moore, 1989, Genomics.

Characterization, mapping, and expression of the human ceruloplasmin gene.

S. Naylor, G. S. Adrian, F. Yang, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Organization and Chromosomal Locations of Genes Encoding Human Plasma Proteins

S. Naylor, J. Lum, J. McGill, 1985 .

Use of chromosome microdissection, the polymerase chain reaction, and dot blot hybridization to analyze double minute chromosomes.

J. Belli, R. Eberle, M. Tucker, 1994, Genetic analysis, techniques and applications.

Reproduction in XYY males: two new cases and implications for genetic counseling.

C. Scott, C. Moore, R. Young, 1984, American journal of medical genetics.

In Situ Hybridization for Chromosomal Mapping of Plasma Proteins

J. McGill, C. Moore, J. McCombs, 1985 .

Deletions of the long arm of chromosome 6: two new cases and review of the literature.

C. Moore, K. Hansen, G. Fidone, 1985, American journal of medical genetics.

A complex chromosomal rearrangement and congenital anomalies in the progeny of a mother treated for childhood leukemia.

C. Daeschner, B. Rouse, L. Lockhart, 1990, Cancer genetics and cytogenetics.

Chromosome localization of the human renin gene (REN) by in situ hybridization.

J. Chirgwin, J. McGill, C. Moore, 1987, Cytogenetics and cell genetics.

Characterization of somatic cell hybrids exhibiting extinction of AFP, Albumin and an AFP-HPRT Transgene

C. Hsieh, J. Papaconstantinou, M. Keherly, 1996, Somatic cell and molecular genetics.

Clonal chromosomal abnormalities in Fanconi's anaemia: what do they really mean?

V. Najfeld, B. Alter, A. Scalise, 1993, British journal of haematology.

Rapid detection of poliovirus by reverse transcription and polymerase chain amplification: application for differentiation between poliovirus and nonpoliovirus enteroviruses

B. Prabhakar, T. Chonmaitree, P. Ogra, 1993, Journal of clinical microbiology.

Deletions in chromosome 22q11 region in cervical aortic arch.

D. Sapire, A. Kumar, J. McCombs, 1997, The American journal of cardiology.

Chromosomal localization of group-specific component by in situ hybridization.

F. Yang, J. McGill, C. Moore, 1986, Cytogenetics and cell genetics.

Human α2-HS-glycoprotein localized to 3q27→q29 by in situ hybridization

V. Magnuson, J. McGill, B. Bowman, 1988 .

Human alpha 2-HS-glycoprotein localized to 3q27----q29 by in situ hybridization.

V. Magnuson, F. Yang, J. McGill, 1988, Cytogenetics and cell genetics.

Atrioventricular septal defect with pulmonary atresia in DiGeorge anomaly: expansion of the cardiac phenotype.

D. Sapire, H. Hawkins, L. V. van Mierop, 1996, American journal of medical genetics.

Fragile-X Mental Retardation Syndrome Transmitted Through Intellectually Normal Males: Implications for Genetic Counseling

C. Moore, R. Jorgenson, C. Jaramillo, 1986, Southern medical journal.