AAAAAA

   
Results: 1-8 |
Results: 8
PRENATAL-DIAGNOSIS OF A DE-NOVO TRISOMY 6Q22.2-]6QTER AND MONOSOMY 1PTER-]1P36.3 - CASE-REPORT WITH A 2-YEAR FOLLOW-UP AND A BRIEF REVIEW OF OTHER PRENATAL CASES OF PARTIAL TRISOMY 6Q (VOL 51, PG 115, 1997)
Authors: KULHARYA AS CARLIN ME STETTLER WA HUSLIG M KUKOLICH MK GARCIAHERAS J
Citation: As. Kulharya et al., PRENATAL-DIAGNOSIS OF A DE-NOVO TRISOMY 6Q22.2-]6QTER AND MONOSOMY 1PTER-]1P36.3 - CASE-REPORT WITH A 2-YEAR FOLLOW-UP AND A BRIEF REVIEW OF OTHER PRENATAL CASES OF PARTIAL TRISOMY 6Q (VOL 51, PG 115, 1997), Clinical genetics, 52(4), 1997, pp. 251-251
PRENATAL-DIAGNOSIS OF A DE-NOVO TRISOMY 6Q22.2-]6QTER AND MONOSOMY 1PTER-]1P36.3 - CASE-REPORT WITH A 2-YEAR FOLLOW-UP AND A BRIEF REVIEW OF OTHER PRENATAL CASES OF PARTIAL TRISOMY 6Q
Authors: KULHARYA AS CARLIN ME STETTLER WA HUSLIG M KUKOLICH MK GARCIAHERAS J
Citation: As. Kulharya et al., PRENATAL-DIAGNOSIS OF A DE-NOVO TRISOMY 6Q22.2-]6QTER AND MONOSOMY 1PTER-]1P36.3 - CASE-REPORT WITH A 2-YEAR FOLLOW-UP AND A BRIEF REVIEW OF OTHER PRENATAL CASES OF PARTIAL TRISOMY 6Q, Clinical genetics, 51(2), 1997, pp. 115-117
UNUSUAL FAMILIAL ADD(15) CHROMOSOME CONTAINS NECESSARY Y-GENES FOR FERTILITY
Authors: MOWREY PN GADI IK TEPPERBERG JH ALLAHHAM M KUKOLICH MK PAPENHAUSEN PR
Citation: Pn. Mowrey et al., UNUSUAL FAMILIAL ADD(15) CHROMOSOME CONTAINS NECESSARY Y-GENES FOR FERTILITY, American journal of human genetics, 61(4), 1997, pp. 767-767
MILD PHENOTYPIC EFFECTS OF A DE-NOVO DELETION-XPTER-]XP22.3 AND DUPLICATION-3PTER-]3P23
Authors: KULHARYA AS ROOP H KUKOLICH MK NACHTMAN RG BELMONT JW GARCIAHERAS J
Citation: As. Kulharya et al., MILD PHENOTYPIC EFFECTS OF A DE-NOVO DELETION-XPTER-]XP22.3 AND DUPLICATION-3PTER-]3P23, American journal of medical genetics, 56(1), 1995, pp. 16-21
INTERSTITIAL DELETIONS 4Q21.1Q25 AND 4Q25Q27 - PHENOTYPIC VARIABILITYAND RELATION TO RIEGER ANOMALY
Authors: KULHARYA AS MABERRY M KUKOLICH MK DAY DW SCHNEIDER NR WILSON GN TONK V
Citation: As. Kulharya et al., INTERSTITIAL DELETIONS 4Q21.1Q25 AND 4Q25Q27 - PHENOTYPIC VARIABILITYAND RELATION TO RIEGER ANOMALY, American journal of medical genetics, 55(2), 1995, pp. 165-170
DEFINITION OF A 14 CM CRITICAL REGION FOR AXENFELD-RIEGER SYNDROME ATCHROMOSOME 4Q25-27
Authors: MIRZAYANS F TONK V KUKOLICH MK PEARCE WG WALTER MA
Citation: F. Mirzayans et al., DEFINITION OF A 14 CM CRITICAL REGION FOR AXENFELD-RIEGER SYNDROME ATCHROMOSOME 4Q25-27, American journal of human genetics, 57(4), 1995, pp. 1137-1137
MOLECULAR AND CYTOGENETIC STUDIES ON A DE-NOVO DELETION XPTER-]XP22.3AND DUPLICATION 3PTER-]3P23 ASSOCIATED WITH MILD DYSMORPHIA AND SPEECH DELAY
Authors: KULHARYA AS ROOP H KUKOLICH MK NACHTMAN RG BELMONT JW GARCIAHERAS J
Citation: As. Kulharya et al., MOLECULAR AND CYTOGENETIC STUDIES ON A DE-NOVO DELETION XPTER-]XP22.3AND DUPLICATION 3PTER-]3P23 ASSOCIATED WITH MILD DYSMORPHIA AND SPEECH DELAY, American journal of human genetics, 53(3), 1993, pp. 569-569
TRISOMY 6QTER-]6Q22.2 AND MONOSOMY 1PTER-]1P36.3 IDENTIFIED BY FISH AT AMNIOCENTESIS
Authors: GARCIAHERAS J KULHARYA AS STETTLER WA CARLIN ME GOULD M KUKOLICH MK
Citation: J. Garciaheras et al., TRISOMY 6QTER-]6Q22.2 AND MONOSOMY 1PTER-]1P36.3 IDENTIFIED BY FISH AT AMNIOCENTESIS, American journal of human genetics, 53(3), 1993, pp. 1570-1570
Risultati: 1-8 |