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Results:
1-20
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Results: 20
Authors:
SLACK JL
ARTHUR DC
LAWRENCE D
MROZEK K
MAYER RJ
DAVEY FR
TANTRAVAHI R
PETTENATI MJ
BIGNER S
CARROLL AJ
RAO KW
SCHIFFER CA
BLOOMFIELD CD
Citation: Jl. Slack et al., SECONDARY CYTOGENETIC CHANGES IN ACUTE PROMYELOCYTIC LEUKEMIA - PROGNOSTIC IMPORTANCE IN PATIENTS TREATED WITH CHEMOTHERAPY ALONE AND ASSOCIATION WITH THE INTRON-3 BREAKPOINT OF THE PML GENE - A CANCER AND LEUKEMIA GROUP-B STUDY, Journal of clinical oncology, 15(5), 1997, pp. 1786-1795
Authors:
MROZEK K
HEINONEN K
LAWRENCE D
CARROLL AJ
KODURU PRK
RAO KW
SCHIFFER CA
BLOOMFIELD CD
Citation: K. Mrozek et al., T(9-11)(P22-Q23) CONFERS BETTER PROGNOSIS THAN OTHER TRANSLOCATIONS OF 11Q23 IN ADULTS WITH DE-NOVO ACUTE MYELOID-LEUKEMIA (AML) - A CANCERAND LEUKEMIA GROUP-B STUDY, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 332-332
Authors:
HANSEN WF
BERNARD LE
LANGLOIS S
RAO KW
CHESCHEIR NC
AYLSWORTH AS
SMITH DI
ROBINSON WP
BARRETT IJ
KALOUSEK DK
Citation: Wf. Hansen et al., MATERNAL UNIPARENTAL DISOMY OF CHROMOSOME-2 AND CONFINED PLACENTAL MOSAICISM FOR TRISOMY-2 IN A FETUS WITH INTRAUTERINE GROWTH RESTRICTION,HYPOSPADIAS, AND OLIGOHYDRAMNIOS, Prenatal diagnosis, 17(5), 1997, pp. 443-450
Authors:
FU KL
TENFOE JLR
JOENJE H
RAO KW
LIU JM
WALSH CE
Citation: Kl. Fu et al., FUNCTIONAL CORRECTION OF FANCONI-ANEMIA GROUP-A HEMATOPOIETIC-CELLS BY RETROVIRAL GENE-TRANSFER, Blood, 90(9), 1997, pp. 3296-3303
Authors:
MROZEK K
HEINONEN K
LAWRENCE D
CARROLL AJ
KODURU PRK
RAO KW
STROUT MP
HUTCHISON RE
MOORE JO
MAYER RJ
SCHIFFER CA
BLOOMFIELD CD
Citation: K. Mrozek et al., ADULT PATIENTS WITH DE-NOVO ACUTE MYELOID-LEUKEMIA AND T(9-11)(P22-Q23) HAVE A SUPERIOR OUTCOME TO PATIENTS WITH OTHER TRANSLOCATIONS INVOLVING BAND 11Q23 - A CANCER AND LEUKEMIA GROUP-B STUDY, Blood, 90(11), 1997, pp. 4532-4538
Authors:
FU KL
LO JR
TENFOE JRL
JOENJE H
RAO KW
LIU JM
WALSH CE
Citation: Kl. Fu et al., FUNCTIONAL CORRECTION OF FANCONI-ANEMIA GROUP-A HEMATOPOIETIC-CELLS -CLINICAL AND DIAGNOSTIC IMPLICATIONS, Blood, 90(10), 1997, pp. 1926-1926
Authors:
JOSEPH GL
KAISERROGERS KA
RAO KW
Citation: Gl. Joseph et al., A RETROSPECTIVE SEARCH FOR 1P36 DELETIONS IN 48 PATIENTS WITH A PRADER-WILLI-LIKE PHENOTYPE USING METAPHASE FISH, American journal of human genetics, 61(4), 1997, pp. 728-728
Authors:
KAISERROGERS KA
POWELL CM
CALLANAN NP
LEDBETTER DH
SUSSMAN DS
RAO KW
Citation: Ka. Kaiserrogers et al., THE USEFULNESS AND LIMITATIONS OF USING FISH TO CHARACTERIZE 2 PARTIALLY CRYPTIC COMPLEX CHROMOSOME REARRANGEMENTS, American journal of human genetics, 61(4), 1997, pp. 731-731
Authors:
PHILLIPS KK
KAISERROGERS KA
EUBANKS S
RAO KW
Citation: Kk. Phillips et al., PRENATAL-DIAGNOSIS OF AN INVERSION X(Q26.3Q28) IN A FAMILY WITH A FERTILE FEMALE AND AN APPARENTLY FERTILE MALE, American journal of human genetics, 61(4), 1997, pp. 783-783
Authors:
WELLS SR
KULLER JA
RAO KW
AYLSWORTH AS
Citation: Sr. Wells et al., MULTIPLE CONGENITAL-MALFORMATIONS IN AN INFANT PRENATALLY DIAGNOSED WITH MOSAICISM FOR DUP(1Q) AND DEL(XQ), Clinical genetics, 49(4), 1996, pp. 216-219
Authors:
ESTABROOKS LL
RAO KW
DRISCOLL DA
CRANDALL BF
DEAN JCS
IKONEN E
KORF B
AYLSWORTH AS
Citation: Ll. Estabrooks et al., PRELIMINARY PHENOTYPIC MAP OF CHROMOSOME 4P16 BASED ON 4P DELETIONS, American journal of medical genetics, 57(4), 1995, pp. 581-586
Authors:
PETTENATI MJ
RAO PN
PHELAN MC
GRASS F
RAO KW
COSPER P
CARROLL AJ
ELDER F
SMITH JL
HIGGINS MD
LANMAN JT
HIGGINS RR
BUTLER MG
LUTHARDT F
KEITGES E
JACKSONCOOK C
BROWN J
SCHWARTZ S
VANDYKE DL
PALMER CG
Citation: Mj. Pettenati et al., PARACENTRIC INVERSIONS IN HUMANS - A REVIEW OF 446 PARACENTRIC INVERSIONS WITH PRESENTATION OF 120 NEW CASES, American journal of medical genetics, 55(2), 1995, pp. 171-187
Authors:
BERNARD LE
KALOUSEK DK
LANGLOIS S
BARRETT IJ
HANSEN WF
AYLSWORTH AS
SMITH DI
RAO KW
Citation: Le. Bernard et al., CONFINED PLACENTAL MOSAICISM FOR TRISOMY-2 WITH FETAL MATERNAL UNIPARENTAL DISOMY OF CHROMOSOME, American journal of human genetics, 57(4), 1995, pp. 261-261
Authors:
POWELL CM
REITNAUER PJ
KAISERROGERS KA
RAO KW
Citation: Cm. Powell et al., A PARACENTRIC INVERSION OF 16Q IN A PATIENT WITH ANUS, HAND, AND EAR ANOMALIES - FURTHER EVIDENCE FOR A TOWNES-BROCKS SYNDROME GENE AT 16Q12.1, American journal of human genetics, 57(4), 1995, pp. 552-552
Authors:
KAISERROGERS KA
DAVENPORT ML
POWELL CM
RAO KW
Citation: Ka. Kaiserrogers et al., A RECOMBINANT X-CHROMOSOME WITH AN ATYPICAL CENTROMERE OBSERVED IN A CHILD WITH TURNER-SYNDROME, American journal of human genetics, 57(4), 1995, pp. 658-658
Authors:
REITNAUER PJ
ALBRIGHT SG
AYLSWORTH AS
POWELL CM
KAISERROGERS KA
RAO KW
Citation: Pj. Reitnauer et al., A SUBTLE FAMILIAL TRANSLOCATION-11-22 ASSOCIATED WITH MACROCEPHALY INBALANCED CARRIERS, American journal of human genetics, 57(4), 1995, pp. 695-695
Authors:
ALBRIGHT SG
LACHIEWICZ AM
TARLETON JC
RAO KW
SCHWARTZ CE
RICHIE R
TENNISON MB
AYLSWORTH AS
Citation: Sg. Albright et al., FRAGILE-X PHENOTYPE IN A PATIENT WITH A LARGE DE-NOVO DELETION IN XQ27-Q28, American journal of medical genetics, 51(4), 1994, pp. 294-297
Authors:
ESTABROOKS LL
LAMB AN
AYLSWORTH AS
CALLANAN NP
RAO KW
Citation: Ll. Estabrooks et al., MOLECULAR CHARACTERIZATION OF CHROMOSOME 4P DELETIONS RESULTING IN WOLF-HIRSCHHORN SYNDROME, Journal of Medical Genetics, 31(2), 1994, pp. 103-107
Authors:
TEPPERBERG JH
TENNISON MB
KAISERROGERS K
ALBRIGHT SG
AYLSWORTH AS
RAO KW
Citation: Jh. Tepperberg et al., AN INHERITED CRYPTIC TRANSLOCATION BETWEEN CHROMOSOME-13 AND CHROMOSOME-15, DETECTED BY FISH IN A CHILD WITH ANGELMAN SYNDROME, American journal of human genetics, 53(3), 1993, pp. 609-609
Authors:
ESTABROOKS LL
RAO KW
DRISCOLL DA
IKONEN E
KORF B
CRANDALL BF
AYLSWORTH AS
Citation: Ll. Estabrooks et al., A PRELIMINARY PHENOTYPIC MAP OF CHROMOSOME-4P16, American journal of human genetics, 53(3), 1993, pp. 1288-1288
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