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Results: 1-7 |
Results: 7
REFINED MOLECULAR CHARACTERIZATION OF THE BREAKPOINTS IN SMALL INV DUP(15) CHROMOSOMES
Authors: HUANG B CROLLA JA CHRISTIAN SL WOLFLEDBETTER ME MACHA ME PAPENHAUSEN PN LEDBETTER DH
Citation: B. Huang et al., REFINED MOLECULAR CHARACTERIZATION OF THE BREAKPOINTS IN SMALL INV DUP(15) CHROMOSOMES, Human genetics, 99(1), 1997, pp. 11-17
FISH ANALYSIS IN 100 PATIENTS WITH ISOLATED-LISSENCEPHALY-SEQUENCE (ILS) - LIS1 PROBES SIGNIFICANTLY INCREASE DELETION DETECTION RATE
Authors: PILZ DT MACHA ME PRECHT KS DOBYNS WB SMITH ACM LEDBETTER DH
Citation: Dt. Pilz et al., FISH ANALYSIS IN 100 PATIENTS WITH ISOLATED-LISSENCEPHALY-SEQUENCE (ILS) - LIS1 PROBES SIGNIFICANTLY INCREASE DELETION DETECTION RATE, American journal of human genetics, 61(4), 1997, pp. 162-162
IDENTIFICATION OF 2 CLASSES OF BREAKPOINTS IN SMALL INV DUP(15) CHROMOSOMES CONFIRMS HOTSPOTS FOR CHROMOSOME-15 REARRANGEMENTS
Authors: HUANG B CROLLA JA CHRISTIAN SL WOLFLEDBETTER ME MACHA ME PAPENHAUSEN PN LEDBETTER DH
Citation: B. Huang et al., IDENTIFICATION OF 2 CLASSES OF BREAKPOINTS IN SMALL INV DUP(15) CHROMOSOMES CONFIRMS HOTSPOTS FOR CHROMOSOME-15 REARRANGEMENTS, Cytogenetics and cell genetics, 74(4), 1996, pp. 303-303
LOCALIZATION OF THE 3C SYNDROME OR A PHENOCOPY TO CHROMOSOME 1Q44-QTER
Authors: SMITH ACM DAYSALVATORE DL NING Y MACHA ME CHRISTIAN SL TURNER TH SCIORRA LJ DOBYNS WB LEDBETTER DH
Citation: Acm. Smith et al., LOCALIZATION OF THE 3C SYNDROME OR A PHENOCOPY TO CHROMOSOME 1Q44-QTER, American journal of human genetics, 57(4), 1995, pp. 1320-1320
IDENTIFICATION OF A SUBTLE TRANSLOCATION AND THE USE OF CHROMOSOME PAINTING PROBES IN A FAMILY WITH RECURRENT MISCARRIAGES AND A CHILD WITHMCA
Authors: SPIKES A MACHA ME DUNN R SHAFFER LG
Citation: A. Spikes et al., IDENTIFICATION OF A SUBTLE TRANSLOCATION AND THE USE OF CHROMOSOME PAINTING PROBES IN A FAMILY WITH RECURRENT MISCARRIAGES AND A CHILD WITHMCA, Cytogenetics and cell genetics, 63(4), 1993, pp. 255-255
PRENATAL-DIAGNOSIS AND CLINICAL FINDINGS IN A CASE OF HEXASOMY 12P
Authors: MACHA ME VANDENVEYVER IB MCCASKILL C CARPENTER RJ SHAFFER LG
Citation: Me. Macha et al., PRENATAL-DIAGNOSIS AND CLINICAL FINDINGS IN A CASE OF HEXASOMY 12P, Cytogenetics and cell genetics, 63(4), 1993, pp. 256-256
PRENATAL-DIAGNOSIS AND CLINICAL FINDINGS IN A CASE OF HEXASOMY-12P
Authors: VANDENVEYVER IB MACHA ME MCCASKILL C CARPENTER RJ SHAFFER LG
Citation: Ib. Vandenveyver et al., PRENATAL-DIAGNOSIS AND CLINICAL FINDINGS IN A CASE OF HEXASOMY-12P, American journal of medical genetics, 47(8), 1993, pp. 1171-1174
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