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Results: 1-25 | 26-50 | 51-54
Results: 1-25/54
INCREASED PREVALENCE OF IMMUNOGLOBULIN-A DEFICIENCY IN PATIENTS WITH THE CHROMOSOME 22Q11.2 DELETION SYNDROME (DIGEORGE-SYNDROME VELOCARDIOFACIAL SYNDROME)
Authors: SMITH CA DRISCOLL DA EMANUEL BS MCDONALDMCGINN DM ZACKAI EH SULLIVAN KE
Citation: Ca. Smith et al., INCREASED PREVALENCE OF IMMUNOGLOBULIN-A DEFICIENCY IN PATIENTS WITH THE CHROMOSOME 22Q11.2 DELETION SYNDROME (DIGEORGE-SYNDROME VELOCARDIOFACIAL SYNDROME), Clinical and diagnostic laboratory immunology, 5(3), 1998, pp. 415-417
FREQUENCY OF 22Q11 DELETIONS IN PATIENTS WITH CONOTRUNCAL DEFECTS
Authors: GOLDMUNTZ E CLARK BJ MITCHELL LE JAWAD AF CUNEO BF REED L MCDONALDMCGINN D CHIEN P FEUER J ZACKAI EH EMANUEL BS DRISCOLL DA
Citation: E. Goldmuntz et al., FREQUENCY OF 22Q11 DELETIONS IN PATIENTS WITH CONOTRUNCAL DEFECTS, Journal of the American College of Cardiology, 32(2), 1998, pp. 492-498
CAT EYE SYNDROME CHROMOSOME BREAKPOINT CLUSTERING - IDENTIFICATION OF2 INTERVALS ALSO ASSOCIATED WITH 22Q11 DELETION SYNDROME BREAKPOINTS
Authors: MCTAGGART KE BUDARF ML DRISCOLL DA EMANUEL BS FERREIRA P MCDERMID HE
Citation: Ke. Mctaggart et al., CAT EYE SYNDROME CHROMOSOME BREAKPOINT CLUSTERING - IDENTIFICATION OF2 INTERVALS ALSO ASSOCIATED WITH 22Q11 DELETION SYNDROME BREAKPOINTS, Cytogenetics and cell genetics, 81(3-4), 1998, pp. 222-228
DEVELOPMENTAL PRESENTATION OF 22Q11.2 DELETION (DIGEORGE VELOCARDIOFACIAL-SYNDROME)/
Authors: WANG PP SOLOT C MOSS EM GERDES M MCDONALDMCGINN DM DRISCOLL DA EMANUEL BS ZACKAI EH
Citation: Pp. Wang et al., DEVELOPMENTAL PRESENTATION OF 22Q11.2 DELETION (DIGEORGE VELOCARDIOFACIAL-SYNDROME)/, Journal of developmental and behavioral pediatrics, 19(5), 1998, pp. 342-345
7 NEW CASES OF CAYLER CARDIOFACIAL SYNDROME WITH CHROMOSOME 22Q11.2 DELETION, INCLUDING A FAMILIAL CASE
Authors: BAWLE EV CONARD J VANDYKE DL CZARNECKI P DRISCOLL DA
Citation: Ev. Bawle et al., 7 NEW CASES OF CAYLER CARDIOFACIAL SYNDROME WITH CHROMOSOME 22Q11.2 DELETION, INCLUDING A FAMILIAL CASE, American journal of medical genetics, 79(5), 1998, pp. 406-410
LACK OF CORRELATION BETWEEN IMPAIRED T-CELL PRODUCTION, IMMUNODEFICIENCY, AND OTHER PHENOTYPIC FEATURES IN CHROMOSOME 22Q11.2 DELETION SYNDROMES (DIGEORGE-SYNDROME VELOCARDIOFACIAL SYNDROME)
Authors: SULLIVAN KE JAWAD AF RANDALL P DRISCOLL DA EMANUEL BS MCDONALDMCGINN DM ZACKAI EH
Citation: Ke. Sullivan et al., LACK OF CORRELATION BETWEEN IMPAIRED T-CELL PRODUCTION, IMMUNODEFICIENCY, AND OTHER PHENOTYPIC FEATURES IN CHROMOSOME 22Q11.2 DELETION SYNDROMES (DIGEORGE-SYNDROME VELOCARDIOFACIAL SYNDROME), Clinical immunology and immunopathology, 86(2), 1998, pp. 141-146
GROWTH-HORMONE DEFICIENCY IN PATIENTS WITH A 22Q11.2 DELETION - EXPANDING THE PHENOTYPE
Authors: WEINZIMER SA MCDONALDMCGINN DM DRISCOLL DA EMANUEL BS ZACKAI EH MOSHANG T
Citation: Sa. Weinzimer et al., GROWTH-HORMONE DEFICIENCY IN PATIENTS WITH A 22Q11.2 DELETION - EXPANDING THE PHENOTYPE, Pediatrics, 101(5), 1998, pp. 929-932
GENETIC-STRUCTURE OF THE FROGS GEOCRINIA-LUTEA AND GEOCRINIA-ROSEA REFLECTS EXTREME POPULATION DIVERGENCE AND RANGE CHANGES, NOT DISPERSAL BARRIERS
Authors: DRISCOLL DA
Citation: Da. Driscoll, GENETIC-STRUCTURE OF THE FROGS GEOCRINIA-LUTEA AND GEOCRINIA-ROSEA REFLECTS EXTREME POPULATION DIVERGENCE AND RANGE CHANGES, NOT DISPERSAL BARRIERS, Evolution, 52(4), 1998, pp. 1147-1157
GENETIC-STRUCTURE, METAPOPULATION PROCESSES AND EVOLUTION INFLUENCE THE CONSERVATION STRATEGIES FOR 2 ENDANGERED FROG SPECIES
Authors: DRISCOLL DA
Citation: Da. Driscoll, GENETIC-STRUCTURE, METAPOPULATION PROCESSES AND EVOLUTION INFLUENCE THE CONSERVATION STRATEGIES FOR 2 ENDANGERED FROG SPECIES, Biological Conservation, 83(1), 1998, pp. 43-54
CHARACTERIZATION OF 10P DELETIONS SUGGESTS 2 NONOVERLAPPING REGIONS CONTRIBUTE TO THE DIGEORGE-SYNDROME PHENOTYPE
Authors: GOTTLIEB S DRISCOLL DA PUNNETT HH SELLINGER B EMANUEL BS BUDARF ML
Citation: S. Gottlieb et al., CHARACTERIZATION OF 10P DELETIONS SUGGESTS 2 NONOVERLAPPING REGIONS CONTRIBUTE TO THE DIGEORGE-SYNDROME PHENOTYPE, American journal of human genetics, 62(2), 1998, pp. 495-498
CLONING AND EXPRESSION OF PRIMATE DAXX CDNAS AND MAPPING OF THE HUMANGENE TO CHROMOSOME 6P21.3 IN THE MHC REGION
Authors: KIRIAKIDOU M DRISCOLL DA LOPEZGUISA JM STRAUSS JF
Citation: M. Kiriakidou et al., CLONING AND EXPRESSION OF PRIMATE DAXX CDNAS AND MAPPING OF THE HUMANGENE TO CHROMOSOME 6P21.3 IN THE MHC REGION, DNA and cell biology, 16(11), 1997, pp. 1289-1298
STRUCTURAL AND MUTATIONAL ANALYSIS OF A CONSERVED GENE (DGSI) FROM THE MINIMAL DIGEORGE-SYNDROME CRITICAL REGION
Authors: GONG WL EMANUEL BS GALILI N KIM DH ROE B DRISCOLL DA BUDARF ML
Citation: Wl. Gong et al., STRUCTURAL AND MUTATIONAL ANALYSIS OF A CONSERVED GENE (DGSI) FROM THE MINIMAL DIGEORGE-SYNDROME CRITICAL REGION, Human molecular genetics, 6(2), 1997, pp. 267-276
IMPACT OF FUEL-REDUCTION BURNING ON THE FROG GEOCRINIA-LUTEA IN SOUTHWEST WESTERN-AUSTRALIA
Authors: DRISCOLL DA ROBERTS JD
Citation: Da. Driscoll et Jd. Roberts, IMPACT OF FUEL-REDUCTION BURNING ON THE FROG GEOCRINIA-LUTEA IN SOUTHWEST WESTERN-AUSTRALIA, Australian journal of ecology, 22(3), 1997, pp. 334-339
MOBILITY AND METAPOPULATION STRUCTURE OF GEOCRINIA-ALBA AND GEOCRINIA-VITELLINA, 2 ENDANGERED FROG SPECIES FROM SOUTHWESTERN AUSTRALIA
Authors: DRISCOLL DA
Citation: Da. Driscoll, MOBILITY AND METAPOPULATION STRUCTURE OF GEOCRINIA-ALBA AND GEOCRINIA-VITELLINA, 2 ENDANGERED FROG SPECIES FROM SOUTHWESTERN AUSTRALIA, Australian journal of ecology, 22(2), 1997, pp. 185-195
SKELETAL ANOMALIES AND DEFORMITIES IN PATIENTS WITH DELETIONS OF 22Q11
Authors: MING JE MCDONALDMCGINN DM MEGERIAN TE DRISCOLL DA ELIAS ER RUSSELL BM IRONS M EMANUEL BS MARKOWITZ RI ZACKAI EH
Citation: Je. Ming et al., SKELETAL ANOMALIES AND DEFORMITIES IN PATIENTS WITH DELETIONS OF 22Q11, American journal of medical genetics, 72(2), 1997, pp. 210-215
UNBALANCED 15-22 TRANSLOCATION IN A PATIENT WITH MANIFESTATIONS OF DIGEORGE-SYNDROME AND VELOCARDIOFACIAL SYNDROME
Authors: JAQUEZ M DRISCOLL DA LI MR EMANUEL BS HERNANDEZ I JAQUEZ F LEMBERT N RAMIREZ J MATALON R
Citation: M. Jaquez et al., UNBALANCED 15-22 TRANSLOCATION IN A PATIENT WITH MANIFESTATIONS OF DIGEORGE-SYNDROME AND VELOCARDIOFACIAL SYNDROME, American journal of medical genetics, 70(1), 1997, pp. 6-10
NASAL DIMPLE AS PART OF THE 22Q11.2 DELETION SYNDROME
Authors: GRIPP KW MCDONALDMCGINN DM DRISCOLL DA REED LA EMANUEL BS ZACKAI EH
Citation: Kw. Gripp et al., NASAL DIMPLE AS PART OF THE 22Q11.2 DELETION SYNDROME, American journal of medical genetics, 69(3), 1997, pp. 290-292
EVOLUTION OF LATENT HYPOPARATHYROIDISM IN FAMILIAL 22Q11 DELETION SYNDROME
Authors: CUNEO BF DRISCOLL DA GIDDING SS LANGMAN CB
Citation: Bf. Cuneo et al., EVOLUTION OF LATENT HYPOPARATHYROIDISM IN FAMILIAL 22Q11 DELETION SYNDROME, American journal of medical genetics, 69(1), 1997, pp. 50-55
DETECTION OF A 22Q11.2 DELETION IN CARDIAC PATIENTS SUGGESTS A RISK FOR VELOPHARYNGEAL INCOMPETENCE
Authors: MCDONALDMCGINN DM DRISCOLL DA EMANUEL BS GOLDMUNTZ E CLARK BJ SOLOT C COHEN M SCHULTZ P LAROSSA D RANDALL P ZACKAI EH
Citation: Dm. Mcdonaldmcginn et al., DETECTION OF A 22Q11.2 DELETION IN CARDIAC PATIENTS SUGGESTS A RISK FOR VELOPHARYNGEAL INCOMPETENCE, Pediatrics, 99(5), 1997, pp. 91-95
SUCCESSFUL FORMATION OF A CHIMERIC HUMAN THYMUS ALLOGRAFT FOLLOWING TRANSPLANTATION OF CULTURED POSTNATAL HUMAN THYMUS
Authors: MARKERT ML KOSTYU DD WARD FE MCLAUGHLIN TM WATSON TJ BUCKLEY RH SCHIFF SE UNGERLEIDER RM GAYNOR JW OLDHAM KT MAHAFFEY SM BALLOW M DRISCOLL DA HALE LP HAYNES BF
Citation: Ml. Markert et al., SUCCESSFUL FORMATION OF A CHIMERIC HUMAN THYMUS ALLOGRAFT FOLLOWING TRANSPLANTATION OF CULTURED POSTNATAL HUMAN THYMUS, The Journal of immunology, 158(2), 1997, pp. 998-1005
JUVENILE RHEUMATOID ARTHRITIS-LIKE POLYARTHRITIS IN CHROMOSOME 22Q11.2 DELETION SYNDROME (DIGEORGE ANOMALAD VELOCARDIOFACIAL SYNDROME CONOTRUNCAL ANOMALY FACE SYNDROME)
Authors: SULLIVAN KE MCDONALDMCGINN DM DRISCOLL DA ZMIJEWSKI CM ELLABBAN AS REED L EMANUEL BS ZACKAI EH ATHREYA BH KEENAN G
Citation: Ke. Sullivan et al., JUVENILE RHEUMATOID ARTHRITIS-LIKE POLYARTHRITIS IN CHROMOSOME 22Q11.2 DELETION SYNDROME (DIGEORGE ANOMALAD VELOCARDIOFACIAL SYNDROME CONOTRUNCAL ANOMALY FACE SYNDROME), Arthritis and rheumatism, 40(3), 1997, pp. 430-436
SCREENING CARDIAC PATIENTS FOR 22Q11.2 DELETIONS
Authors: DRISCOLL DA EMANUEL BS BUDARF ML
Citation: Da. Driscoll et al., SCREENING CARDIAC PATIENTS FOR 22Q11.2 DELETIONS, American journal of human genetics, 61(4), 1997, pp. 160-160
THE DIGEORGE-SYNDROME MINIMAL CRITICAL REGION CONTAINS A GOOSECOID-LIKE (GSCL) HOMEOBOX GENE THAT IS EXPRESSED EARLY IN HUMAN-DEVELOPMENT
Authors: GOTTLIEB S EMANUEL BS DRISCOLL DA SELLINGER B WANG ZL ROE B BUDARF ML
Citation: S. Gottlieb et al., THE DIGEORGE-SYNDROME MINIMAL CRITICAL REGION CONTAINS A GOOSECOID-LIKE (GSCL) HOMEOBOX GENE THAT IS EXPRESSED EARLY IN HUMAN-DEVELOPMENT, American journal of human genetics, 60(5), 1997, pp. 1194-1201
RECOGNITION OF TUBE-OVARIAN ABSCESS IN ADOLESCENTS WITH PELVIC INFLAMMATORY DISEASE
Authors: SLAP GB FORKE CM CNAAN A BELLAH RD KREIDER ME HANISSIAN JA GALLAGHER PR DRISCOLL DA
Citation: Gb. Slap et al., RECOGNITION OF TUBE-OVARIAN ABSCESS IN ADOLESCENTS WITH PELVIC INFLAMMATORY DISEASE, Journal of adolescent health, 18(6), 1996, pp. 397-403
KABUKI SYNDROME IS NOT CAUSED BY A MICRO DELETION IN THE DIGEORGE VELOCARDIOFACIAL CHROMOSOMAL REGION WITHIN 22Q11.2/
Authors: LI MR ZACKAI EH NIIKAWA N KAPLAN P DRISCOLL DA
Citation: Mr. Li et al., KABUKI SYNDROME IS NOT CAUSED BY A MICRO DELETION IN THE DIGEORGE VELOCARDIOFACIAL CHROMOSOMAL REGION WITHIN 22Q11.2/, American journal of medical genetics, 65(2), 1996, pp. 101-103
Risultati: 1-25 | 26-50 | 51-54