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Results: 1-17 |
Results: 17
CEREBRO-OCULO-NASAL-SYNDROME - ANOTHER CASE AND REVIEW OF THE LITERATURE
Authors: ERCAL D SAY B
Citation: D. Ercal et B. Say, CEREBRO-OCULO-NASAL-SYNDROME - ANOTHER CASE AND REVIEW OF THE LITERATURE, Clinical dysmorphology, 7(2), 1998, pp. 139-141
INDUCTION OF AGAMOUS GENE-EXPRESSION PLAYS A KEY ROLE IN RIPENING OF TOMATO SEPALS IN-VITRO
Authors: ISHIDA BK JENKINS SM SAY B
Citation: Bk. Ishida et al., INDUCTION OF AGAMOUS GENE-EXPRESSION PLAYS A KEY ROLE IN RIPENING OF TOMATO SEPALS IN-VITRO, Plant molecular biology, 36(5), 1998, pp. 733-739
LETTER TO THE EDITOR - PULMONARY AGENESIS - IMPORTANCE OF DETAILED CYTOGENETIC STUDIES
Authors: SAY B CARPENTER NJ
Citation: B. Say et Nj. Carpenter, LETTER TO THE EDITOR - PULMONARY AGENESIS - IMPORTANCE OF DETAILED CYTOGENETIC STUDIES, American journal of medical genetics, 76(5), 1998, pp. 446-446
NOVEL MUTATION IN THE FGFR2 GENE AT THE SAME CODON AS THE CROUZON-SYNDROME MUTATIONS IN A SEVERE PFEIFFER-SYNDROME TYPE-2 CASE
Authors: SCHAEFER F ANDERSON C CAN B SAY B
Citation: F. Schaefer et al., NOVEL MUTATION IN THE FGFR2 GENE AT THE SAME CODON AS THE CROUZON-SYNDROME MUTATIONS IN A SEVERE PFEIFFER-SYNDROME TYPE-2 CASE, American journal of medical genetics, 75(3), 1998, pp. 252-255
2 SISTERS WITH DIFFERENT CHROMOSOMAL MICRODELETIONS - RUBINSTEIN-TAYBI-SYNDROME AND 22Q DELETION SYNDROME
Authors: CAN B QU Y JACKSON LG FLOYD M SAY B
Citation: B. Can et al., 2 SISTERS WITH DIFFERENT CHROMOSOMAL MICRODELETIONS - RUBINSTEIN-TAYBI-SYNDROME AND 22Q DELETION SYNDROME, Clinical genetics, 54(4), 1998, pp. 371-372
INV DUP(13)(QTERQ21.1) WITH NEOCENTROMERE IN 13Q32 - PRECISE DEFINITION OF DUPLICATION AND CENTROMERE LOCATION USING CENP ANTIBODIES AND FISH
Authors: WARBURTON D PERRICONE L SAY B CARPENTER N YU CY WARBURTON PE
Citation: D. Warburton et al., INV DUP(13)(QTERQ21.1) WITH NEOCENTROMERE IN 13Q32 - PRECISE DEFINITION OF DUPLICATION AND CENTROMERE LOCATION USING CENP ANTIBODIES AND FISH, American journal of human genetics, 61(4), 1997, pp. 812-812
MIDLINE FIELD DEFECTS AND HIRSCHSPRUNG DISEASE
Authors: SAY B SMITH DP
Citation: B. Say et Dp. Smith, MIDLINE FIELD DEFECTS AND HIRSCHSPRUNG DISEASE, American journal of medical genetics, 61(3), 1996, pp. 293-294
DETECTION OF A FAMILIAL CRYPTIC TRANSLOCATION BY FLUORESCENT IN-SITU HYBRIDIZATION
Authors: SMITH DP FLOYD M SAY B
Citation: Dp. Smith et al., DETECTION OF A FAMILIAL CRYPTIC TRANSLOCATION BY FLUORESCENT IN-SITU HYBRIDIZATION, Journal of Medical Genetics, 33(1), 1996, pp. 84-84
FAMILIAL DELETION OF CHROMOSOME-18 (P11.2)
Authors: VELAGALETI GVN HARRIS S CARPENTER NJ COLDWELL J SAY B
Citation: Gvn. Velagaleti et al., FAMILIAL DELETION OF CHROMOSOME-18 (P11.2), Annales de genetique, 39(4), 1996, pp. 201-204
PARTIAL TRISOMY 13Q IDENTIFIED BY SEQUENTIAL FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: RAO VVNG CARPENTER NJ GUCSAVAS M COLDWELL J SAY B
Citation: Vvng. Rao et al., PARTIAL TRISOMY 13Q IDENTIFIED BY SEQUENTIAL FLUORESCENCE IN-SITU HYBRIDIZATION, American journal of medical genetics, 58(1), 1995, pp. 50-53
CD1-TUBE DEFECTS( CELLS IN MOTHERS OF STILLBORN INFANTS WITH NEURAL)
Authors: SENIZ FN MUFTUOGLU E BATUN MS SAY B
Citation: Fn. Seniz et al., CD1-TUBE DEFECTS( CELLS IN MOTHERS OF STILLBORN INFANTS WITH NEURAL), American journal of medical genetics, 56(1), 1995, pp. 60-61
MATERNAL SERUM-FREE BETA-HCG SCREENING - RESULTS OF STUDIES INCLUDING480 CASES OF DOWN-SYNDROME
Authors: MACRI JN SPENCER K GARVER K BUCHANAN PD SAY B CARPENTER NJ MULLER F BOUE A
Citation: Jn. Macri et al., MATERNAL SERUM-FREE BETA-HCG SCREENING - RESULTS OF STUDIES INCLUDING480 CASES OF DOWN-SYNDROME, Prenatal diagnosis, 14(2), 1994, pp. 97-103
AASE-SMITH SYNDROME - REPORT OF A NEW CASE WITH UNUSUAL FEATURES
Authors: YETGIN S BALCI S IRKEN G COSKUN T SAY B
Citation: S. Yetgin et al., AASE-SMITH SYNDROME - REPORT OF A NEW CASE WITH UNUSUAL FEATURES, Turkish Journal of Pediatrics, 36(3), 1994, pp. 239-242
DOWN-SYNDROME PHENOTYPES - THE CONSEQUENCES OF CHROMOSOMAL IMBALANCE (VOL 91, PG 4997, 1994)
Authors: KORENBERG JR CHEN XN SCHIPPER R SUN Z GONSKY R GERWEHR S CARPENTER N DAUMER C DIGNAN P DISTECHE C GRAHAM JM HUDGINS L MCGILLIVRAY B MIYAZAKI K OGASAWARA N PARK JP PAGON R PUESCHEL S SACK G SAY B SCHUFFENHAUER S SOUKUP S YAMANAKA T
Citation: Jr. Korenberg et al., DOWN-SYNDROME PHENOTYPES - THE CONSEQUENCES OF CHROMOSOMAL IMBALANCE (VOL 91, PG 4997, 1994), Proceedings of the National Academy of Sciences of the United Statesof America, 91(23), 1994, pp. 11281-11281
DOWN-SYNDROME PHENOTYPES - THE CONSEQUENCES OF CHROMOSOMAL IMBALANCE
Authors: KORENBERG JR CHEN XN SCHIPPER R SUN Z GONSKY R GERWEHR S CARPENTER N DAUMER C DIGNAN P DISTECHE C GRAHAM JM HUGDINS L MCGILLIVRAY B MIYAZAKI K OGASAWARA N PARK JP PAGON R PUESCHEL S SACK G SAY B SCHUFFENHAUER S SOUKUP S YAMANAKA T
Citation: Jr. Korenberg et al., DOWN-SYNDROME PHENOTYPES - THE CONSEQUENCES OF CHROMOSOMAL IMBALANCE, Proceedings of the National Academy of Sciences of the United Statesof America, 91(11), 1994, pp. 4997-5001
THE COSTELLO SYNDROME
Authors: SAY B GUCSAVAS M MORGAN H YORK C
Citation: B. Say et al., THE COSTELLO SYNDROME, American journal of medical genetics, 47(2), 1993, pp. 163-165
COMPLEX DOWN-SYNDROME CHROMOSOMES - MOLECULAR DEFINITION USING FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: CHEN XN KORENBERG JR CARPENTER N SUN ZG SCHIPPER R NOYA D SAY B
Citation: Xn. Chen et al., COMPLEX DOWN-SYNDROME CHROMOSOMES - MOLECULAR DEFINITION USING FLUORESCENCE IN-SITU HYBRIDIZATION, American journal of human genetics, 53(3), 1993, pp. 531-531
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