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Results: 1-15 |
Results: 15
RANDOM X INACTIVATION IN A FEMALE WITH A BALANCED T(X-9) AND AN ABNORMAL PHENOTYPE
Authors: ZACKOWSKI JL SCHWARTZ S MONTGOMERY T WOLFF DJ
Citation: Jl. Zackowski et al., RANDOM X INACTIVATION IN A FEMALE WITH A BALANCED T(X-9) AND AN ABNORMAL PHENOTYPE, Cytogenetics and cell genetics, 82(1-2), 1998, pp. 143-143
RANDOM X-INACTIVATION IN A GIRL WITH A BALANCED T(X-9) AND AN ABNORMAL PHENOTYPE
Authors: WOLFF DJ SCHWARTZ S MONTGOMERY T ZACKOWSKI JL
Citation: Dj. Wolff et al., RANDOM X-INACTIVATION IN A GIRL WITH A BALANCED T(X-9) AND AN ABNORMAL PHENOTYPE, American journal of medical genetics, 77(5), 1998, pp. 401-404
CHARACTERIZATION OF NEO-CENTROMERES IN MARKER CHROMOSOMES LACKING DETECTABLE ALPHA-SATELLITE DNA
Authors: DEPINET TW ZACKOWSKI JL EARNSHAW WC KAFFE S SEKHON GS STALLARD R SULLIVAN BA VANCE GH VANDYKE DL WILLARD HF ZINN AB SCHWARTZ S
Citation: Tw. Depinet et al., CHARACTERIZATION OF NEO-CENTROMERES IN MARKER CHROMOSOMES LACKING DETECTABLE ALPHA-SATELLITE DNA, Human molecular genetics, 6(8), 1997, pp. 1195-1204
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
PRENATAL DETECTION AND DELINEATION BY FISH OF PARTIAL MONOSOMY 9Q ANDTRISOMY-12 RESULTING FROM A SUBTLE PATERNAL RECIPROCAL INSERTION
Authors: ZACKOWSKI JL EARLEY KA PHILLIPS SE SURKA WS PROUD VK ABUHAMAD AZ SCHWARTZ S
Citation: Jl. Zackowski et al., PRENATAL DETECTION AND DELINEATION BY FISH OF PARTIAL MONOSOMY 9Q ANDTRISOMY-12 RESULTING FROM A SUBTLE PATERNAL RECIPROCAL INSERTION, American journal of human genetics, 61(4), 1997, pp. 824-824
NON-MOSAIC TETRASOMY 9P IN A LIVEBORN INFANT WITH MULTIPLE CONGENITAL-ANOMALIES - CASE-REPORT AND COMPARISON WITH TRISOMY 9P
Authors: LEICHTMAN LG ZACKOWSKI JL STORTO PD NEWLIN A
Citation: Lg. Leichtman et al., NON-MOSAIC TETRASOMY 9P IN A LIVEBORN INFANT WITH MULTIPLE CONGENITAL-ANOMALIES - CASE-REPORT AND COMPARISON WITH TRISOMY 9P, American journal of medical genetics, 63(3), 1996, pp. 434-437
MOSAICISM FOR STRUCTURAL CHROMOSOME-ABERRATIONS - RESULTS OF A SURVEY
Authors: ZACKOWSKI JL
Citation: Jl. Zackowski, MOSAICISM FOR STRUCTURAL CHROMOSOME-ABERRATIONS - RESULTS OF A SURVEY, Cytogenetics and cell genetics, 71(4), 1995, pp. 395-395
ESTIMATION FROM FISH DATA OF THE TOTAL FREQUENCY OF ANEUPLOIDY IN HUMAN SPERM
Authors: HOEGERMAN SF PANG MG ZACKOWSKI JL KEARNS WG
Citation: Sf. Hoegerman et al., ESTIMATION FROM FISH DATA OF THE TOTAL FREQUENCY OF ANEUPLOIDY IN HUMAN SPERM, Cytogenetics and cell genetics, 71(4), 1995, pp. 396-396
PARACENTRIC INVERSION OF CHROMOSOME-1 INHERITED FROM A MOSAIC FATHER
Authors: ZACKOWSKI JL NEWLIN A LEICHTMAN LG NEU RL
Citation: Jl. Zackowski et al., PARACENTRIC INVERSION OF CHROMOSOME-1 INHERITED FROM A MOSAIC FATHER, Cytogenetics and cell genetics, 69(1-2), 1995, pp. 117-117
REPRODUCTIVE OUTCOME IN 3 FAMILIES WITH A SATELLITED CHROMOSOME-4 WITH REVIEW OF THE LITERATURE
Authors: ARN PH YOUNIE L RUSSO S ZACKOWSKI JL MANKINEN C ESTABROOKS L
Citation: Ph. Arn et al., REPRODUCTIVE OUTCOME IN 3 FAMILIES WITH A SATELLITED CHROMOSOME-4 WITH REVIEW OF THE LITERATURE, American journal of medical genetics, 57(3), 1995, pp. 420-424
DETECTION BY FLUORESCENCE IN-SITU HYBRIDIZATION OF CHROMOSOME-4, CHROMOSOME-6, CHROMOSOME-7, CHROMOSOME-8, CHROMOSOME-9, CHROMOSOME-10, CHROMOSOME-11, CHROMOSOME-12, CHROMOSOME-13, CHROMOSOME-17, CHROMOSOME-18, CHROMOSOME-21, CHROMOSOME-X AND CHROMOSOME-Y ANEUPLOIDY IN SPERM FROM OLIGO-ASTHENO-TERATO-ZOOSPERMIC PATIENTS OF AN IN-VITRO FERTILIZATION PROGRAM
Authors: PANG MG ZACKOWSKI JL HOEGERMAN SF FRIEDMAN E MOON SY CUTICCHIA AJ ACOSTA AA KEARNS WG
Citation: Mg. Pang et al., DETECTION BY FLUORESCENCE IN-SITU HYBRIDIZATION OF CHROMOSOME-4, CHROMOSOME-6, CHROMOSOME-7, CHROMOSOME-8, CHROMOSOME-9, CHROMOSOME-10, CHROMOSOME-11, CHROMOSOME-12, CHROMOSOME-13, CHROMOSOME-17, CHROMOSOME-18, CHROMOSOME-21, CHROMOSOME-X AND CHROMOSOME-Y ANEUPLOIDY IN SPERM FROM OLIGO-ASTHENO-TERATO-ZOOSPERMIC PATIENTS OF AN IN-VITRO FERTILIZATION PROGRAM, American journal of human genetics, 57(4), 1995, pp. 680-680
ARE SPECIFIC SHORT ARM VARIANTS OR HETEROMORPHISMS OVER-REPRESENTED IN THE CHROMOSOME-15 DELETION IN ANGELMAN OR PRADER-WILLI-SYNDROME PATIENTS - REPLY
Authors: ZACKOWSKI JL BENTWILLIAMS A GRAY BA
Citation: Jl. Zackowski et al., ARE SPECIFIC SHORT ARM VARIANTS OR HETEROMORPHISMS OVER-REPRESENTED IN THE CHROMOSOME-15 DELETION IN ANGELMAN OR PRADER-WILLI-SYNDROME PATIENTS - REPLY, American journal of medical genetics, 50(1), 1994, pp. 45-45
A CASE OF OF 45, X 46, X DIC(Y) DIAGNOSED PRENATALLY/
Authors: ZACKOWSKI JL LONG CK STORTO PD
Citation: Jl. Zackowski et al., A CASE OF OF 45, X 46, X DIC(Y) DIAGNOSED PRENATALLY/, Cytogenetics and cell genetics, 63(4), 1993, pp. 251-252
CLINICAL, CYTOGENETIC, AND MOLECULAR EVIDENCE FOR AN INFANT WITH SMITH-MAGENIS SYNDROME BORN FROM A MOTHER HAVING A MOSAIC 17P11.2P12 DELETION
Authors: ZORI RT LUPSKI JR ZHANG HJ GREENBERG F KILLIAN JM GRAY BA DRISCOLL DJ PATEL PI ZACKOWSKI JL
Citation: Rt. Zori et al., CLINICAL, CYTOGENETIC, AND MOLECULAR EVIDENCE FOR AN INFANT WITH SMITH-MAGENIS SYNDROME BORN FROM A MOTHER HAVING A MOSAIC 17P11.2P12 DELETION, American journal of medical genetics, 47(4), 1993, pp. 504-511
PREAXIAL ACROFACIAL DYSOSTOSIS (NAGER SYNDROME) ASSOCIATED WITH AN INHERITED AND APPARENTLY BALANCED X-9 TRANSLOCATION - PRENATAL AND POSTNATAL LATE REPLICATION STUDIES
Authors: ZORI RT GRAY BA BENTWILLIAMS A DRISCOLL DJ WILLIAMS CA ZACKOWSKI JL
Citation: Rt. Zori et al., PREAXIAL ACROFACIAL DYSOSTOSIS (NAGER SYNDROME) ASSOCIATED WITH AN INHERITED AND APPARENTLY BALANCED X-9 TRANSLOCATION - PRENATAL AND POSTNATAL LATE REPLICATION STUDIES, American journal of medical genetics, 46(4), 1993, pp. 379-383
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