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Results: 1-9 |
Results: 9
DOUBLE TRANSFER OF CLEAVAGE-STAGE EMBRYOS FOLLOWED BY BLASTOCYSTS IN CASES OF REPEATED IVF FAILURE
Authors: SAFRAN A SHAYOVITS A PORATKATZ A NEIGER M EISENBERG V BENSHUSHAN A REUBINOFF B SCHENKER J BAREL H LEWIN A
Citation: A. Safran et al., DOUBLE TRANSFER OF CLEAVAGE-STAGE EMBRYOS FOLLOWED BY BLASTOCYSTS IN CASES OF REPEATED IVF FAILURE, Human reproduction (Oxford. Print), 13, 1998, pp. 30-30
BLASTOCYST CULTURE AS A MEANS TO SELECT VIABLE EMBRYOS FROM EMBRYOS FOUND TO BE UNSUITABLE FOR CRYOPRESERVATION
Authors: SAFRAN A NEIGER M SHAYOVITS A PORATKATZ A EISENBERG V BENSHUSHAN A REUBINOFF B SCHENKER J BAREL H LEWIN A
Citation: A. Safran et al., BLASTOCYST CULTURE AS A MEANS TO SELECT VIABLE EMBRYOS FROM EMBRYOS FOUND TO BE UNSUITABLE FOR CRYOPRESERVATION, Human reproduction (Oxford. Print), 13, 1998, pp. 117-117
DELETION (4)(Q33-]QTER) - A CASE-REPORT AND REVIEW OF THE LITERATURE
Authors: BOROCHOWITZ Z SHALEV SA YEHUDAI I BAREL H DAR H TIROSH E
Citation: Z. Borochowitz et al., DELETION (4)(Q33-]QTER) - A CASE-REPORT AND REVIEW OF THE LITERATURE, Journal of child neurology, 12(5), 1997, pp. 335-337
INHERITED INVERTED DUPLICATION OF X-CHROMOSOME IN A MALE - REPORT OF A PATIENT AND REVIEW OF THE LITERATURE
Authors: SHAPIRA M DAR H BAREL H BARNITZAN N EVEN L BOROCHOWITZ Z
Citation: M. Shapira et al., INHERITED INVERTED DUPLICATION OF X-CHROMOSOME IN A MALE - REPORT OF A PATIENT AND REVIEW OF THE LITERATURE, American journal of medical genetics, 72(4), 1997, pp. 409-414
THE CONTRIBUTION OF FLUORESCENCE IN-SITU HYBRIDIZATION (FISH) AND PCRTECHNIQUES TO THE DIAGNOSIS OF A CRYPTIC COMPLEX TRANSLOCATION IN A CASE OF ESSENTIAL-THROMBOCYTOPENIA - (ET)
Authors: DAR H BAREL H ZIV M DAOUD M BRAESTER A
Citation: H. Dar et al., THE CONTRIBUTION OF FLUORESCENCE IN-SITU HYBRIDIZATION (FISH) AND PCRTECHNIQUES TO THE DIAGNOSIS OF A CRYPTIC COMPLEX TRANSLOCATION IN A CASE OF ESSENTIAL-THROMBOCYTOPENIA - (ET), American journal of human genetics, 61(4), 1997, pp. 339-339
UPPER-LIMB MALFORMATIONS IN CHROMOSOME 22Q11 DELETIONS
Authors: SHALEV SA DAR H BAREL H BOROCHOWITZ Z
Citation: Sa. Shalev et al., UPPER-LIMB MALFORMATIONS IN CHROMOSOME 22Q11 DELETIONS, American journal of medical genetics, 62(3), 1996, pp. 302-302
VERY-LOW MATERNAL SERUM UNCONJUGATED ESTRIOL AND PRENATAL-DIAGNOSIS OF STEROID SULFATASE DEFICIENCY
Authors: DAVID M ISRAEL N MERKSAMER R BARNIZAN N BOROCHOWITZ Z BAREL H YEHUDAI I DAR H
Citation: M. David et al., VERY-LOW MATERNAL SERUM UNCONJUGATED ESTRIOL AND PRENATAL-DIAGNOSIS OF STEROID SULFATASE DEFICIENCY, Fetal diagnosis and therapy, 10(2), 1995, pp. 76-80
NEW HERITABLE FRAGILE SITE WITH SPONTANEOUS EXPRESSION AT 1Q41
Authors: DAR H BAREL H ZIV M SHAPIRO I
Citation: H. Dar et al., NEW HERITABLE FRAGILE SITE WITH SPONTANEOUS EXPRESSION AT 1Q41, American journal of medical genetics, 55(2), 1995, pp. 145-146
DELETION OF THE SHORT ARM, OF CHROMOSOME-10 (10P13) - REPORT OF A PATIENT AND REVIEW
Authors: SHAPIRA M BOROCHOWITZ Z BAREL H DAR H ETZIONI A LORBER A
Citation: M. Shapira et al., DELETION OF THE SHORT ARM, OF CHROMOSOME-10 (10P13) - REPORT OF A PATIENT AND REVIEW, American journal of medical genetics, 52(1), 1994, pp. 34-38
Risultati: 1-9 |