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Results: 1-14 |
Results: 14

Authors: ESTOP AM MUNNE S CIEPLY KM VANDERMARK KK LAMB AN FISCH H
Citation: Am. Estop et al., MEIOTIC PRODUCTS OF A KLINEFELTER 47,XXY MALE AS DETERMINED BY SPERM FLUORESCENCE IN-SITU HYBRIDIZATION ANALYSIS, Human reproduction, 13(1), 1998, pp. 124-127

Authors: SANDLIN CJ LAMB AN KERSHBERG HB PRECHT KS LESE CM LEDBETTER DH HUANG B
Citation: Cj. Sandlin et al., JUMPING TRANSLOCATIONS INVOLVING THE Y-CHROMOSOME IN A FAMILY, American journal of human genetics, 61(4), 1997, pp. 793-793

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

Authors: RICHKIND KE LAMB AN WASON D LYTLE C VELASCO J
Citation: Ke. Richkind et al., PROSPECTIVE EVALUATION OF FISH ANALYSIS FOR HEMATOLOGIC MALIGNANCIES, Blood, 86(10), 1995, pp. 3094-3094

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

Authors: LAMB AN PETTENATI M HANNA J KRASIKOV N NEU R RAO N WEINSTEIN M WEISER J ESTABROOKS L
Citation: An. Lamb et al., 6 CASES OF SATELLITED LONG ARM OF CHROMOSOME-2 DETECTED DURING PRENATAL CHROMOSOME DIAGNOSIS, American journal of human genetics, 57(4), 1995, pp. 1642-1642

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: NEU RL LYTLE CH RYAN SL WEINSTEIN ME LAMB AN
Citation: Rl. Neu et al., EXAMPLES OF THE PRACTICAL APPLICATION OF FISH TECHNOLOGY IN THE DIAGNOSTIC CYTOGENETIC LABORATORY, Cytogenetics and cell genetics, 63(4), 1993, pp. 254-254

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

Authors: KRASIKOV N LAMB AN VETRANO LA HANSEN JL MENGES DE LYTLE CH ROHERTY SL DAVENPORT MB PAUKER S DOLKART L DAVIS G
Citation: N. Krasikov et al., BENIGN VARIANT 8P23.1, American journal of human genetics, 53(3), 1993, pp. 568-568

Authors: ROHERTY S LYTLE CH LAMB AN
Citation: S. Roherty et al., DISCREPANCY BETWEEN CYTOGENETIC AND FISH ANALYSIS FOR DELETION DETECTION IN PRADER-WILLI AND ANGELMAN SYNDROMES, American journal of human genetics, 53(3), 1993, pp. 594-594

Authors: TOWNER J CARVAJAL MV MOSCATELLO D LYTLE C GALLAGHER T NEU RL LACASSIE Y LAMB AN
Citation: J. Towner et al., ABNORMAL PHENOTYPE ASSOCIATED WITH AN INHERITED AND WITH A DE-NOVO INV DUP(15) MARKER CHROMOSOME - DETECTION OF EUCHROMATIC SEQUENCES USINGPROBES FROM THE PWS AS DELETION REGIONS/, American journal of human genetics, 53(3), 1993, pp. 612-612

Authors: RANDOLPH LM LAMB AN
Citation: Lm. Randolph et An. Lamb, MOLECULAR CONFIRMATION OF CYTOGENETIC DELETION IS VITAL IN PRADER-WILLI-SYNDROME AND ANGELMAN SYNDROME, American journal of human genetics, 53(3), 1993, pp. 1752-1752

Authors: LAMB AN LYTLE CH ROHERTY S SAPETA M THEVES R WARD BE
Citation: An. Lamb et al., ANEUPLOIDY DETECTION IN UNCULTURED AMNIOCYTES - INTERSITE TRANSFER OFINTERPHASE FISH TECHNOLOGY, American journal of human genetics, 53(3), 1993, pp. 1802-1802
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