AAAAAA

   
Results: 1-9 |
Results: 9
DOPAMINE TRANSPORTER-1 (DAT-1) POLYMORPHISMS AND ATTENTION-DEFICIT HYPERACTIVITY DISORDER
Authors: LAFORTE SC MCCOMBS JL
Citation: Sc. Laforte et Jl. Mccombs, DOPAMINE TRANSPORTER-1 (DAT-1) POLYMORPHISMS AND ATTENTION-DEFICIT HYPERACTIVITY DISORDER, Journal of investigative medicine, 46(1), 1998, pp. 9-9
DELETIONS IN CHROMOSOME 22Q11 REGION IN CERVICAL AORTIC-ARCH
Authors: KUMAR A MCCOMBS JL SAPIRE DW
Citation: A. Kumar et al., DELETIONS IN CHROMOSOME 22Q11 REGION IN CERVICAL AORTIC-ARCH, The American journal of cardiology, 79(3), 1997, pp. 388
CHARACTERIZATION OF SOMATIC-CELL HYBRIDS EXHIBITING EXTINCTION OF AFP, ALBUMIN AND AN AFP-HPRT TRANSGENE
Authors: KEHERLY MJ HSIEH CC MCCOMBS JL MERRYMAN LS PAPACONSTANTINOU J
Citation: Mj. Keherly et al., CHARACTERIZATION OF SOMATIC-CELL HYBRIDS EXHIBITING EXTINCTION OF AFP, ALBUMIN AND AN AFP-HPRT TRANSGENE, Somatic cell and molecular genetics, 22(2), 1996, pp. 119-134
ATRIOVENTRICULAR SEPTAL-DEFECT WITH PULMONARY ATRESIA IN DIGEORGE ANOMALY - EXPANSION OF THE CARDIAC PHENOTYPE
Authors: KUMAR A SAPIRE DW LOCKHART LH MCCOMBS JL HAWKINS HK VANMIEROP LHS
Citation: A. Kumar et al., ATRIOVENTRICULAR SEPTAL-DEFECT WITH PULMONARY ATRESIA IN DIGEORGE ANOMALY - EXPANSION OF THE CARDIAC PHENOTYPE, American journal of medical genetics, 61(1), 1996, pp. 89-91
ASSOCIATION OF CERVICAL AORTIC-ARCH WITH DELETIONS IN CHROMOSOME 22Q11.2 REGION
Authors: KUMAR A MCCOMBS JL SAPIRE DW
Citation: A. Kumar et al., ASSOCIATION OF CERVICAL AORTIC-ARCH WITH DELETIONS IN CHROMOSOME 22Q11.2 REGION, Pediatric research, 39(4), 1996, pp. 169-169
IS TETRALOGY OF FALLOT PART OF THE SPECTRUM OF DIGEORGE AND RELATED SYNDROMES - CORRELATION OF THE PHENOTYPE TO MICRODELETION IN CHROMOSOME22Q11
Authors: KUMAR A MCCOMBS JL LOCKHART LH PEARL W SAPIRE DW
Citation: A. Kumar et al., IS TETRALOGY OF FALLOT PART OF THE SPECTRUM OF DIGEORGE AND RELATED SYNDROMES - CORRELATION OF THE PHENOTYPE TO MICRODELETION IN CHROMOSOME22Q11, Pediatric research, 37(4), 1995, pp. 28-28
MICRODELETION IN CHROMOSOME 22Q11.2 IN CONOTRUNCAL CARDIAC DEFECTS
Authors: KUMAR A MCCOMBS JL MOLLER M LOCKHART LH PEARL W SAPIRE DW
Citation: A. Kumar et al., MICRODELETION IN CHROMOSOME 22Q11.2 IN CONOTRUNCAL CARDIAC DEFECTS, Circulation, 92(8), 1995, pp. 2471-2471
A SEQUENTIAL STAINING TECHNIQUE FOR KARYOTYPIC ANALYSIS OF INTERSPECIFIC SOMATIC-CELL HYBRIDS
Authors: KEHERLY MJ PAPACONSTANTINOU J MCCOMBS JL
Citation: Mj. Keherly et al., A SEQUENTIAL STAINING TECHNIQUE FOR KARYOTYPIC ANALYSIS OF INTERSPECIFIC SOMATIC-CELL HYBRIDS, Experimental cell research, 205(2), 1993, pp. 361-364
PRIMER DIRECTED IN-SITU HYBRIDIZATION - AMPLIFICATION AND LOCALIZATION OF SPECIFIC SEQUENCES ON METAPHASE CHROMOSOMES
Authors: MCCOMBS JL LOCKHART LL
Citation: Jl. Mccombs et Ll. Lockhart, PRIMER DIRECTED IN-SITU HYBRIDIZATION - AMPLIFICATION AND LOCALIZATION OF SPECIFIC SEQUENCES ON METAPHASE CHROMOSOMES, American journal of human genetics, 53(3), 1993, pp. 1326-1326
Risultati: 1-9 |