AAAAAA

   
Results: 1-11 |
Results: 11
TRANSIENT THERAPY-RELATED MYELODYSPLASTIC SYNDROME-ASSOCIATED WITH MONOSOMY-7 AND 11Q23 TRANSLOCATION
Authors: LAVER JH YUSUF U CANTU ES BARREDO JC HOLT LB ABBOUD MR
Citation: Jh. Laver et al., TRANSIENT THERAPY-RELATED MYELODYSPLASTIC SYNDROME-ASSOCIATED WITH MONOSOMY-7 AND 11Q23 TRANSLOCATION, Leukemia, 11(3), 1997, pp. 448-450
ALL PATIENTS WITH THE T(11-16)(Q23-P13.3) THAT INVOLVES MLL AND CBP HAVE TREATMENT-RELATED HEMATOLOGIC DISORDERS
Authors: ROWLEY JD RESHMI S SOBULO O MUSVEE T ANASTASI J RAIMONDI S SCHNEIDER NR BARREDO JC CANTU ES SCHLEGELBERGER B BEHM F DOGGETT NA BORROW J ZELEZNIKLE N
Citation: Jd. Rowley et al., ALL PATIENTS WITH THE T(11-16)(Q23-P13.3) THAT INVOLVES MLL AND CBP HAVE TREATMENT-RELATED HEMATOLOGIC DISORDERS, Blood, 90(2), 1997, pp. 535-541
EVIDENCE IMPLICATING THE 22Q11 REGION IN THE DEVELOPMENT OF A WILMS-TUMOR ASSOCIATED WITH VELOCARDIOFACIAL SYNDROME (VCFS)
Authors: CANTU ES SALINAS CF WRIGHT CF
Citation: Es. Cantu et al., EVIDENCE IMPLICATING THE 22Q11 REGION IN THE DEVELOPMENT OF A WILMS-TUMOR ASSOCIATED WITH VELOCARDIOFACIAL SYNDROME (VCFS), American journal of human genetics, 61(4), 1997, pp. 517-517
MOSAIC VS NONMOSAIC TRISOMY-9 - REPORT OF A LIVEBORN INFANT EVALUATEDBY FLUORESCENCE IN-SITU HYBRIDIZATION AND REVIEW OF THE LITERATURE
Authors: CANTU ES EICHER DJ PAI GS DONAHUE CJ HARLEY RA
Citation: Es. Cantu et al., MOSAIC VS NONMOSAIC TRISOMY-9 - REPORT OF A LIVEBORN INFANT EVALUATEDBY FLUORESCENCE IN-SITU HYBRIDIZATION AND REVIEW OF THE LITERATURE, American journal of medical genetics, 62(4), 1996, pp. 330-335
XP PSEUDOAUTOSOMAL GENE HAPLOINSUFFICIENCY AND LINEAR GROWTH DEFICIENCY IN 3 GIRLS WITH CHROMOSOME XP22-YQ11 TRANSLOCATION
Authors: JOSEPH M CANTU ES PAI GS WILLI SM PAPENHAUSEN PR WEISS L
Citation: M. Joseph et al., XP PSEUDOAUTOSOMAL GENE HAPLOINSUFFICIENCY AND LINEAR GROWTH DEFICIENCY IN 3 GIRLS WITH CHROMOSOME XP22-YQ11 TRANSLOCATION, Journal of Medical Genetics, 33(11), 1996, pp. 906-911
THE HUMAN PALMITOYL-COA LIGASE (FACL2) GENE MAPS TO THE CHROMOSOME 4Q34-Q35 REGION BY FLUORESCENCE IN-SITU HYBRIDIZATION (FISH) AND SOMATIC-CELL HYBRID PANELS
Authors: CANTU ES SPRINKLE TJ GHOSH B SINGH I
Citation: Es. Cantu et al., THE HUMAN PALMITOYL-COA LIGASE (FACL2) GENE MAPS TO THE CHROMOSOME 4Q34-Q35 REGION BY FLUORESCENCE IN-SITU HYBRIDIZATION (FISH) AND SOMATIC-CELL HYBRID PANELS, Genomics, 28(3), 1995, pp. 600-602
AN ATYPICAL TURNER SYNDROME PATIENT WITH RING X-CHROMOSOME MOSAICISM
Authors: CANTU ES JACOBS DF PAI GS
Citation: Es. Cantu et al., AN ATYPICAL TURNER SYNDROME PATIENT WITH RING X-CHROMOSOME MOSAICISM, Annals of clinical and laboratory science, 25(1), 1995, pp. 60-65
CLINICAL PROFILE OF PATIENTS WITH CHROMOSOME 22Q11 MICRODELETION AT THE DIGEORGE LOCUS
Authors: JOSEPH M CANTU ES JASTRAZAB JM SALINAS CF PAI GS
Citation: M. Joseph et al., CLINICAL PROFILE OF PATIENTS WITH CHROMOSOME 22Q11 MICRODELETION AT THE DIGEORGE LOCUS, American journal of human genetics, 57(4), 1995, pp. 510-510
TRICHORHINOPHALANGEAL SYNDROME TYPE-II (LANGER-GIEDION) WITH BILATERAL AGENESIS OF TIBIA AND FIRST METATARSUS IN A BOY WITH 8Q INTERSTITIAL
Authors: SALINAS CF CANTU ES PAI GS TURLEAU C
Citation: Cf. Salinas et al., TRICHORHINOPHALANGEAL SYNDROME TYPE-II (LANGER-GIEDION) WITH BILATERAL AGENESIS OF TIBIA AND FIRST METATARSUS IN A BOY WITH 8Q INTERSTITIAL, American journal of human genetics, 57(4), 1995, pp. 560-560
MENTAL-RETARDATION (MR) IN ULLRICH-TURNER SYNDROME (UTS)
Authors: CANTU ES HAMMOND LS PAI GS
Citation: Es. Cantu et al., MENTAL-RETARDATION (MR) IN ULLRICH-TURNER SYNDROME (UTS), American journal of human genetics, 53(3), 1993, pp. 411-411
INFANTILE SYSTEMIC HYALINOSIS - NEW CRANIOFACIAL AND ORODENTAL FINDINGS IN A BLACK FEMALE
Authors: SALINAS CF SAHN EE REID TR CANTU ES HUTCHINS AR
Citation: Cf. Salinas et al., INFANTILE SYSTEMIC HYALINOSIS - NEW CRANIOFACIAL AND ORODENTAL FINDINGS IN A BLACK FEMALE, American journal of human genetics, 53(3), 1993, pp. 499-499
Risultati: 1-11 |