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Results: 1-11 |
Results: 11
ANTIBODY DEFICIENCY IN WOLF-HIRSCHHORN-SYNDROME
Authors: HANLEYLOPEZ J ESTABROOKS LL STIEHM ER
Citation: J. Hanleylopez et al., ANTIBODY DEFICIENCY IN WOLF-HIRSCHHORN-SYNDROME, The Journal of pediatrics, 133(1), 1998, pp. 141-143
PRENATAL-DIAGNOSIS OF PARTIAL TRISOMY 15Q INHERITED FROM A UNIQUE MATERNAL 15-22 TRANSLOCATION
Authors: YARDMAN SG IINUMA K LYTLE CH ROBINETT SJ CONAWAY NK ESTABROOKS LL
Citation: Sg. Yardman et al., PRENATAL-DIAGNOSIS OF PARTIAL TRISOMY 15Q INHERITED FROM A UNIQUE MATERNAL 15-22 TRANSLOCATION, Cytogenetics and cell genetics, 74(4), 1996, pp. 303-303
DOES REMOVAL OF AMNIOTIC-FLUID FOR PRENATAL INTERPHASE FISH AFFECT TURN-AROUND TIME OF CHROMOSOME ANALYSIS
Authors: ESTABROOKS LL LYTLE CH VOSS J TAKACS JE SANDOW JM SAPETA MJ LAMB AN
Citation: Ll. Estabrooks et al., DOES REMOVAL OF AMNIOTIC-FLUID FOR PRENATAL INTERPHASE FISH AFFECT TURN-AROUND TIME OF CHROMOSOME ANALYSIS, Cytogenetics and cell genetics, 74(4), 1996, pp. 312-312
GENE CANDIDATES FOR HOLOPROSENCEPHALY AND PROGRESSIVE MYOCLONUS EPILEPSY ON 21Q22.3 ISOLATED BY DIRECT SELECTION TECHNIQUE
Authors: YAMAKAWA K COLBEM S BRUSILOVSKIY A HUBERT R MITCHELL S SUN Z CHEN XN ESTABROOKS LL SHIZUYA H KIM UJ BIRREN B SIMON M KORENBERG JR
Citation: K. Yamakawa et al., GENE CANDIDATES FOR HOLOPROSENCEPHALY AND PROGRESSIVE MYOCLONUS EPILEPSY ON 21Q22.3 ISOLATED BY DIRECT SELECTION TECHNIQUE, Cytogenetics and cell genetics, 70(3-4), 1995, pp. 177-177
ALBRIGHT HEREDITARY OSTEODYSTROPHY AND DEL(2)(Q37.3) IN 4 UNRELATED INDIVIDUALS
Authors: PHELAN MC ROGERS RC CLARKSON KB BOWYER FP LEVINE MA ESTABROOKS LL SEVERSON MC DOBYNS WB
Citation: Mc. Phelan et al., ALBRIGHT HEREDITARY OSTEODYSTROPHY AND DEL(2)(Q37.3) IN 4 UNRELATED INDIVIDUALS, American journal of medical genetics, 58(1), 1995, pp. 1-7
PRELIMINARY PHENOTYPIC MAP OF CHROMOSOME 4P16 BASED ON 4P DELETIONS
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
SUMMARY OF THE 1993 ASHG ANCILLARY MEETING - RECENT RESEARCH ON CHROMOSOME-4P SYNDROMES AND GENES
Authors: ESTABROOKS LL BREG WR HAYDEN MR LEDBETTER DH MYERS RM WYANDT HE YANGFENG TL HIRSCHHORN K
Citation: Ll. Estabrooks et al., SUMMARY OF THE 1993 ASHG ANCILLARY MEETING - RECENT RESEARCH ON CHROMOSOME-4P SYNDROMES AND GENES, American journal of medical genetics, 55(4), 1995, pp. 453-458
PRENATAL INTERPHASE FISH ANALYSIS OF AMNIOCYTES - LONGITUDINAL-STUDY OF ACCURACY AND DETECTION RATES
Authors: CARELLI MP LAMB AN ESTABROOKS LL WARD BE
Citation: Mp. Carelli et al., PRENATAL INTERPHASE FISH ANALYSIS OF AMNIOCYTES - LONGITUDINAL-STUDY OF ACCURACY AND DETECTION RATES, American journal of human genetics, 57(4), 1995, pp. 260-260
MOLECULAR CHARACTERIZATION OF CHROMOSOME 4P DELETIONS RESULTING IN WOLF-HIRSCHHORN SYNDROME
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
A GIRL WITH AN INVERTED DUPLICATED XQ AND AN ABNORMAL PHENOTYPE
Authors: CRANDALL BF LAMB AN ESTABROOKS LL
Citation: Bf. Crandall et al., A GIRL WITH AN INVERTED DUPLICATED XQ AND AN ABNORMAL PHENOTYPE, American journal of human genetics, 53(3), 1993, pp. 539-539
A PRELIMINARY PHENOTYPIC MAP OF CHROMOSOME-4P16
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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