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Results: 1-19 |
Results: 19
SEX-CHROMOSOME MARKERS - CHARACTERIZATION USING FLUORESCENCE IN-SITU HYBRIDIZATION AND REVIEW OF THE LITERATURE
Authors: SCHWARTZ S DEPINET TW LEANACOX J ISADA NB KARSON EM PARK VM PASZTOR LM SHEPPARD LC STALLARD R WOLFF DJ ZINN AB ZURCHER VL ZACKOWSKI JL
Citation: S. Schwartz et al., SEX-CHROMOSOME MARKERS - CHARACTERIZATION USING FLUORESCENCE IN-SITU HYBRIDIZATION AND REVIEW OF THE LITERATURE, American journal of medical genetics, 71(1), 1997, pp. 1-7
RECIPROCAL TRANSLOCATION-4-11 WITH BOTH ADJACENT-1 SEGREGANTS VIABLE WITHIN A FAMILY
Authors: ROGERS JC HARRIS DJ PASZTOR LM
Citation: Jc. Rogers et al., RECIPROCAL TRANSLOCATION-4-11 WITH BOTH ADJACENT-1 SEGREGANTS VIABLE WITHIN A FAMILY, Clinical genetics, 51(4), 1997, pp. 250-256
RING CHROMOSOME-1, MONOSOMY-11 AND HISTOLOGICAL FEATURES OF WILMS-TUMOR
Authors: PASZTOR LM GAROLA R
Citation: Lm. Pasztor et R. Garola, RING CHROMOSOME-1, MONOSOMY-11 AND HISTOLOGICAL FEATURES OF WILMS-TUMOR, American journal of human genetics, 61(4), 1997, pp. 424-424
DOES THE INDICATION FOR AMNIOCENTESIS INFLUENCE THE DECISION TO TERMINATE A PREGNANCY FOLLOWING PRENATAL-DIAGNOSIS OF TRISOMY-21
Authors: BEGLEITER ML ROGERS JC PASZTOR LM HARRIS DJ COWLES TA
Citation: Ml. Begleiter et al., DOES THE INDICATION FOR AMNIOCENTESIS INFLUENCE THE DECISION TO TERMINATE A PREGNANCY FOLLOWING PRENATAL-DIAGNOSIS OF TRISOMY-21, American journal of human genetics, 61(4), 1997, pp. 833-833
CHROMOSOMAL LOCALIZATION OF THE BETA-ADDUCIN GENE TO MOUSE CHROMOSOME-6 AND HUMAN-CHROMOSOME-2
Authors: WHITE RA ANGELONI SV PASZTOR LM
Citation: Ra. White et al., CHROMOSOMAL LOCALIZATION OF THE BETA-ADDUCIN GENE TO MOUSE CHROMOSOME-6 AND HUMAN-CHROMOSOME-2, Mammalian genome, 6(10), 1995, pp. 741-743
ASSIGNMENT OF FGF8 TO HUMAN-CHROMOSOME 10Q25-Q26 - MUTATIONS IN FGF8 MAY BE RESPONSIBLE FOR SOME TYPES OF ACROCEPHALOSYNDACTYLY LINKED TO THIS REGION
Authors: WHITE RA DOWLER LL ANGELONI SV PASZTOR LM MACARTHUR CA
Citation: Ra. White et al., ASSIGNMENT OF FGF8 TO HUMAN-CHROMOSOME 10Q25-Q26 - MUTATIONS IN FGF8 MAY BE RESPONSIBLE FOR SOME TYPES OF ACROCEPHALOSYNDACTYLY LINKED TO THIS REGION, Genomics, 30(1), 1995, pp. 109-111
ASSIGNMENT OF THE TRANSCRIPTION FACTOR GATA4 GENE TO HUMAN-CHROMOSOME-8 AND MOUSE CHROMOSOME-14 - GATA4 IS A CANDIDATE GENE FOR DS (DISORGANIZATION)
Authors: WHITE RA DOWLER LL PASZTOR LM GATSON LL ADKISON LR ANGELONI SV WILSON DB
Citation: Ra. White et al., ASSIGNMENT OF THE TRANSCRIPTION FACTOR GATA4 GENE TO HUMAN-CHROMOSOME-8 AND MOUSE CHROMOSOME-14 - GATA4 IS A CANDIDATE GENE FOR DS (DISORGANIZATION), Genomics, 27(1), 1995, pp. 20-26
IDENTIFICATION OF A FAMILIAL UNBALANCED TRANSLOCATION USING FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: PASZTOR LM BOSSAYT PJ WAUTERS J
Citation: Lm. Pasztor et al., IDENTIFICATION OF A FAMILIAL UNBALANCED TRANSLOCATION USING FLUORESCENCE IN-SITU HYBRIDIZATION, Cytogenetics and cell genetics, 71(4), 1995, pp. 394-394
IDENTIFICATION OF DE-NOVO TRANSLOCATIONS INVOLVING 1P36
Authors: PASZTOR LM HARRIS DJ
Citation: Lm. Pasztor et Dj. Harris, IDENTIFICATION OF DE-NOVO TRANSLOCATIONS INVOLVING 1P36, Cytogenetics and cell genetics, 69(1-2), 1995, pp. 117-117
IDENTIFICATION AND CHARACTERIZATION OF A NOVEL RELATED ADHESION FOCALTYROSINE KINASE (RAFTK) FROM MEGAKARYOCYTES AND BRAIN
Authors: AVRAHAM H LONDON R FU Y OTA S HIREGOWDARA D LI J JIANG S PASZTOR LM WHITE RA GROOPMAN JE AVRAHAM S
Citation: H. Avraham et al., IDENTIFICATION AND CHARACTERIZATION OF A NOVEL RELATED ADHESION FOCALTYROSINE KINASE (RAFTK) FROM MEGAKARYOCYTES AND BRAIN, Blood, 86(10), 1995, pp. 1114-1114
MULTIPLE CONGENITAL-ANOMALIES AND AMBIGUOUS GENITALIA IN A CHILD WITHTRISOMY 7Q
Authors: BEGLEITER ML ZALLES C SCHWARTZ JD HARRIS JD PASZTOR LM
Citation: Ml. Begleiter et al., MULTIPLE CONGENITAL-ANOMALIES AND AMBIGUOUS GENITALIA IN A CHILD WITHTRISOMY 7Q, American journal of human genetics, 57(4), 1995, pp. 597-597
DE-NOVO TRISOMY 6P
Authors: PASZTOR LM ROGERS JC SCHWARTZ ID HARRIS DJ
Citation: Lm. Pasztor et al., DE-NOVO TRISOMY 6P, American journal of human genetics, 57(4), 1995, pp. 684-684
INVERSION DUPLICATION CHROMOSOME-8 WITH DIAPHRAGMATIC-HERNIA
Authors: RINGER K ROGERS J PASZTOR LM
Citation: K. Ringer et al., INVERSION DUPLICATION CHROMOSOME-8 WITH DIAPHRAGMATIC-HERNIA, American journal of human genetics, 57(4), 1995, pp. 696-696
INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME-1 - DEL(1)(PTER-]42.11-Q42.3-]QTER)
Authors: ROGERS JC HARRIS DJ PASZTOR LM
Citation: Jc. Rogers et al., INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME-1 - DEL(1)(PTER-]42.11-Q42.3-]QTER), American journal of human genetics, 57(4), 1995, pp. 700-700
ANOTHER LOOK AT A FAMILY WITH T(8-12) AND HEREDITARY SPHEROCYTOSIS
Authors: HARRIS DJ PASZTOR LM WHITE RA
Citation: Dj. Harris et al., ANOTHER LOOK AT A FAMILY WITH T(8-12) AND HEREDITARY SPHEROCYTOSIS, American journal of human genetics, 57(4), 1995, pp. 1960-1960
EVIDENCE FOR A DISTINCT REGION CAUSING A CAT-LIKE CRY IN PATIENTS WITH 5P DELETIONS
Authors: GERSH M GOODART SA PASZTOR LM HARRIS DJ WEISS L OVERHAUSER J
Citation: M. Gersh et al., EVIDENCE FOR A DISTINCT REGION CAUSING A CAT-LIKE CRY IN PATIENTS WITH 5P DELETIONS, American journal of human genetics, 56(6), 1995, pp. 1404-1410
ANALYSIS OF A DE-NOVO TANDEM DUPLICATION OF DISTAL 22Q
Authors: HARRIS DJ PASZTOR LM
Citation: Dj. Harris et Lm. Pasztor, ANALYSIS OF A DE-NOVO TANDEM DUPLICATION OF DISTAL 22Q, Cytogenetics and cell genetics, 63(4), 1993, pp. 252-252
FAMILIAL TURNER VARIANT WITH A DUPLICATED DELETED X-CHROMOSOME
Authors: PASZTOR LM SCHWARTZ ID
Citation: Lm. Pasztor et Id. Schwartz, FAMILIAL TURNER VARIANT WITH A DUPLICATED DELETED X-CHROMOSOME, Cytogenetics and cell genetics, 63(4), 1993, pp. 252-252
TRANSLOCATION 4 11 WITH BOTH ADJACENT I SEGREGANTS VIABLE WITHIN A FAMILY/
Authors: ROGERS JC HARRIS DJ PASZTOR LM
Citation: Jc. Rogers et al., TRANSLOCATION 4 11 WITH BOTH ADJACENT I SEGREGANTS VIABLE WITHIN A FAMILY/, American journal of human genetics, 53(3), 1993, pp. 593-593
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