Citation: O. Geifmanholtzman et K. Fay, BRIEF CLINICAL REPORT - PRENATAL-DIAGNOSIS OF CONGENITAL MYOTONIC-DYSTROPHY AND COUNSELING OF THE PREGNANT MOTHER - CASE-REPORT AND LITERATURE-REVIEW, American journal of medical genetics, 78(3), 1998, pp. 250-253
Authors:
GEIFMANHOLTZMAN O
KAUFMANN L
GONCHOROFF N
BERNSTEIN I
HOLTZMAN EJ
Citation: O. Geifmanholtzman et al., PRENATAL-DIAGNOSIS OF THE FETAL RHC GENOTYPE FROM PERIPHERAL MATERNALBLOOD, Obstetrics and gynecology, 91(4), 1998, pp. 506-510
Authors:
GEIFMANHOLTZMAN O
BERNSTEIN IM
CAPELESS EL
HAWLEY P
SPECHT LA
BIANCHI DW
Citation: O. Geifmanholtzman et al., INCREASE IN FETAL BREECH PRESENTATION IN FEMALE CARRIERS OF DUCHENNE MUSCULAR-DYSTROPHY, American journal of medical genetics, 73(3), 1997, pp. 276-278
Authors:
GEIFMANHOLTZMAN O
WOJTOWYCZ M
KOSMAS E
ARTAL R
Citation: O. Geifmanholtzman et al., FEMALE ALLOIMMUNIZATION WITH ANTIBODIES KNOWN TO CAUSE HEMOLYTIC-DISEASE, Obstetrics and gynecology, 89(2), 1997, pp. 272-275
Authors:
GEIFMANHOLTZMAN O
CRANE SS
WINDERL L
HOLMES M
Citation: O. Geifmanholtzman et al., PERSISTENT UROGENITAL SINUS - PRENATAL-DIAGNOSIS AND PREGNANCY COMPLICATIONS, American journal of obstetrics and gynecology, 176(3), 1997, pp. 709-711
Citation: O. Geifmanholtzman et al., FIRST-TRIMESTER FETAL RHESUS GENOTYPING FROM PERIPHERAL MATERNAL BLOOD, American journal of human genetics, 61(4), 1997, pp. 873-873
Citation: T. Dye et O. Geifmanholtzman, MATERNAL SERUM SCREEN ACCEPTANCE, ANEUPLOIDY AND CENTRAL-NERVOUS-SYSTEM (CNS) ANOMALIES, American journal of human genetics, 61(4), 1997, pp. 1269-1269
Authors:
GEIFMANHOLTZMAN O
BERNSTEIN IM
BERRY SM
HOLTZMAN EJ
VADNAIS TJ
DEMARIA MA
BIANCHI DW
Citation: O. Geifmanholtzman et al., FETAL RHD GENOTYPING IN FETAL CELLS FLOW-SORTED FROM MATERNAL BLOOD, American journal of obstetrics and gynecology, 174(3), 1996, pp. 818-822
Authors:
GEIFMANHOLTZMAN O
HOLTZMAN EJ
VADNAIS TJ
PHILLIPS VE
CAPELESS EL
BIANCHI DW
Citation: O. Geifmanholtzman et al., DETECTION OF FETAL HLA-DQ-ALPHA SEQUENCES IN MATERNAL BLOOD - A GENDER-INDEPENDENT TECHNIQUE OF FETAL CELL IDENTIFICATION, Prenatal diagnosis, 15(3), 1995, pp. 261-268
Authors:
HOLTZMAN EJ
KOLAKOWSKI LF
GEIFMANHOLTZMAN O
OBRIEN DG
RASOULPOUR M
GUILLOT AP
AUSIELLO DA
Citation: Ej. Holtzman et al., MUTATIONS IN THE VASOPRESSIN V2 RECEPTOR GENE IN 2 FAMILIES WITH NEPHROGENIC DIABETES-INSIPIDUS, Journal of the American Society of Nephrology, 5(2), 1994, pp. 169-176
Citation: O. Geifmanholtzman et al., PRENATAL GENETIC DIAGNOSIS BY ISOLATION AND ANALYSIS OF FETAL CELLS CIRCULATING IN MATERNAL BLOOD, Seminars in perinatology, 18(4), 1994, pp. 366-375