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Results: 1-17 |
Results: 17
MUTATIONS OF THE FORKHEAD WINGED-HELIX GENE, FKHL7, IN PATIENTS WITH AXENFELD-RIEGER ANOMALY/
Authors: MEARS AJ JORDAN T MIRZAYANS F DUBOIS S KUME P PARLEE M RITCH R KOOP B KUO WL COLLINS C MARSHALL J GOULD DB PEARCE W CARLSSON P ENERBACK S MORISSETTE J BHATTACHARYA S HOGAN B RAYMOND V WALTER MA
Citation: Aj. Mears et al., MUTATIONS OF THE FORKHEAD WINGED-HELIX GENE, FKHL7, IN PATIENTS WITH AXENFELD-RIEGER ANOMALY/, American journal of human genetics, 63(5), 1998, pp. 1316-1328
AXENFELD-RIEGER ANOMALY MAPS TO 6P25
Authors: GOULD DB MEARS AJ PEARCE WG WALTER MA
Citation: Db. Gould et al., AXENFELD-RIEGER ANOMALY MAPS TO 6P25, Investigative ophthalmology & visual science, 38(4), 1997, pp. 3728-3728
PHYSICAL MAPPING OF THE IRIDOGONIODYSGENESIS ANOMALY REGION AT 6P25
Authors: MEARS AJ MIRZAYANS F GOULD DB WALTER MA
Citation: Aj. Mears et al., PHYSICAL MAPPING OF THE IRIDOGONIODYSGENESIS ANOMALY REGION AT 6P25, Investigative ophthalmology & visual science, 38(4), 1997, pp. 2692-2692
PHYSICAL AND GENETIC-MAPPING OF THE IGDA LOCUS AT 6P25
Authors: MEARS AJ COLLINS C MIRZAYANS F MYAMBO K WERNICK M KUO WL PEARCE WG WALTER MA
Citation: Aj. Mears et al., PHYSICAL AND GENETIC-MAPPING OF THE IGDA LOCUS AT 6P25, American journal of human genetics, 61(4), 1997, pp. 1665-1665
AUTOSOMAL-DOMINANT AXENFELD-RIEGER ANOMALY MAPS TO 6P25
Authors: GOULD DB MEARS AJ PEARCE WG WALTER MA
Citation: Db. Gould et al., AUTOSOMAL-DOMINANT AXENFELD-RIEGER ANOMALY MAPS TO 6P25, American journal of human genetics, 61(3), 1997, pp. 765-768
IDENTIFICATION OF THE HUMAN CHROMOSOMAL REGION CONTAINING THE IRIDOGONIODYSGENESIS ANOMALY LOCUS BY GENOMIC-MISMATCH SCANNING
Authors: MIRZAYANS F MEARS AJ GUO SW PEARCE WG WALTER MA
Citation: F. Mirzayans et al., IDENTIFICATION OF THE HUMAN CHROMOSOMAL REGION CONTAINING THE IRIDOGONIODYSGENESIS ANOMALY LOCUS BY GENOMIC-MISMATCH SCANNING, American journal of human genetics, 61(1), 1997, pp. 111-119
AUTOSOMAL-DOMINANT IRIDOGONIODYSGENESIS AND AXENFELD-RIEGER SYNDROME ARE GENETICALLY DISTINCT
Authors: WALTER MA MIRZAYANS F MEARS AJ HICKEY K PEARCE WG
Citation: Ma. Walter et al., AUTOSOMAL-DOMINANT IRIDOGONIODYSGENESIS AND AXENFELD-RIEGER SYNDROME ARE GENETICALLY DISTINCT, Ophthalmology, 103(11), 1996, pp. 1907-1915
IRIDOGONIODYSGENESIS IS GENETICALLY DISTINCT FROM AXENFELD-RIEGER SYNDROME
Authors: MEARS AJ PEARCE WG MIRZAYANS F WALTER MA
Citation: Aj. Mears et al., IRIDOGONIODYSGENESIS IS GENETICALLY DISTINCT FROM AXENFELD-RIEGER SYNDROME, Investigative ophthalmology & visual science, 37(3), 1996, pp. 2077-2077
DER(22)T(11-22) RESULTING FROM A PATERNAL DE-NOVO TRANSLOCATION, ADJACENT-1 SEGREGATION, AND MATERNAL HETERODISOMY OF CHROMOSOME-22
Authors: DAWSON AJ MEARS AJ CHUDLEY AE BECHHANSEN T MCDERMID H
Citation: Aj. Dawson et al., DER(22)T(11-22) RESULTING FROM A PATERNAL DE-NOVO TRANSLOCATION, ADJACENT-1 SEGREGATION, AND MATERNAL HETERODISOMY OF CHROMOSOME-22, Journal of Medical Genetics, 33(11), 1996, pp. 952-956
AUTOSOMAL-DOMINANT IRIDOGONIODYSGENESIS ANOMALY MAPS TO 6P25
Authors: MEARS AJ MIRZAYANS F GOULD DB PEARCE WG WALTER MA
Citation: Aj. Mears et al., AUTOSOMAL-DOMINANT IRIDOGONIODYSGENESIS ANOMALY MAPS TO 6P25, American journal of human genetics, 59(6), 1996, pp. 1321-1327
CAT EYE SYNDROME PATIENT WITH INTERSTITIAL DUPLICATION OF CHROMOSOME 22Q11.2
Authors: SELLINGER BT TATSUMURA YO MEARS AJ MCDERMID HE EMANUEL BS BUDARF ML
Citation: Bt. Sellinger et al., CAT EYE SYNDROME PATIENT WITH INTERSTITIAL DUPLICATION OF CHROMOSOME 22Q11.2, Cytogenetics and cell genetics, 71(4), 1995, pp. 394-394
DER(22)T(11-22) DUE TO A PATERNAL DE-NOVO TRANSLOCATION, ADJACENT-1 SEGREGATION AND MATERNAL HETERODISOMY OF CHROMOSOME-22
Authors: DAWSON AJ CHUDLEY AE MEARS AJ BECHHANSEN NT MCDERMID HE
Citation: Aj. Dawson et al., DER(22)T(11-22) DUE TO A PATERNAL DE-NOVO TRANSLOCATION, ADJACENT-1 SEGREGATION AND MATERNAL HETERODISOMY OF CHROMOSOME-22, American journal of human genetics, 57(4), 1995, pp. 623-623
MINUTE SUPERNUMERARY RING CHROMOSOME-22 ASSOCIATED WITH CAT EYE SYNDROME - FURTHER DELINEATION OF THE CRITICAL REGION
Authors: MEARS AJ ELSHANTI H MURRAY JC MCDERMID HE PATIL SR
Citation: Aj. Mears et al., MINUTE SUPERNUMERARY RING CHROMOSOME-22 ASSOCIATED WITH CAT EYE SYNDROME - FURTHER DELINEATION OF THE CRITICAL REGION, American journal of human genetics, 57(3), 1995, pp. 667-673
THE E-SUBUNIT OF VACUOLAR H-ATPASE LOCALIZES CLOSE TO THE CENTROMERE ON HUMAN-CHROMOSOME 22()
Authors: BAUD V MEARS AJ LAMOUR V SCAMPS C DUNCAN AMV MCDERMID HE LIPINSKI M
Citation: V. Baud et al., THE E-SUBUNIT OF VACUOLAR H-ATPASE LOCALIZES CLOSE TO THE CENTROMERE ON HUMAN-CHROMOSOME 22(), Human molecular genetics, 3(2), 1994, pp. 335-339
MAPPING OF THE CRITICAL REGION OF CAT EYE SYNDROME AT 22Q11.2
Authors: MEARS AJ RIAZI MA BUDARF ML EMANUEL BS MURRAY JC PATIL SR MCDERMID HE
Citation: Aj. Mears et al., MAPPING OF THE CRITICAL REGION OF CAT EYE SYNDROME AT 22Q11.2, Cytogenetics and cell genetics, 67(4), 1994, pp. 289-289
A SUBUNIT OF VACUOLAR H-ATPASE IS ENCODED WITHIN THE CAT EYE SYNDROMECRITICAL REGION ON HUMAN-CHROMOSOME-22()
Authors: BAUD V MEARS AJ LAMOUR V SCAMPS C DUNCAN AMV MCDERMID HE LIPINSKI M
Citation: V. Baud et al., A SUBUNIT OF VACUOLAR H-ATPASE IS ENCODED WITHIN THE CAT EYE SYNDROMECRITICAL REGION ON HUMAN-CHROMOSOME-22(), Cytogenetics and cell genetics, 67(4), 1994, pp. 294-294
MOLECULAR CHARACTERIZATION OF THE MARKER CHROMOSOME ASSOCIATED WITH CAT EYE SYNDROME
Authors: MEARS AJ DUNCAN AMV BUDARF ML EMANUEL BS SELLINGER B SIEGELBARTELT J GREENBERG CR MCDERMID HE
Citation: Aj. Mears et al., MOLECULAR CHARACTERIZATION OF THE MARKER CHROMOSOME ASSOCIATED WITH CAT EYE SYNDROME, American journal of human genetics, 55(1), 1994, pp. 134-142
Risultati: 1-17 |