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Results: 1-10 |
Results: 10
THE CLINICAL-SIGNIFICANCE OF ISOLATED ANOMALIES OF THE CORPUS-CALLOSUM ON MR-IMAGING
Authors: FILIPPI CG KIER EL POBER B SCHULZ RJ SALUJA S BRONEN RA
Citation: Cg. Filippi et al., THE CLINICAL-SIGNIFICANCE OF ISOLATED ANOMALIES OF THE CORPUS-CALLOSUM ON MR-IMAGING, Radiology, 205, 1997, pp. 1232-1232
CHARACTERIZATION OF THE WILLIAMS-SYNDROME DELETION REGION ON CHROMOSOME 7Q11.23
Authors: OSBORNE LR SODER S HERBRICK JA POBER B COSTA T SHI XM HENG HHQ GREAVETTE TF SCHERER SW TSUI LC
Citation: Lr. Osborne et al., CHARACTERIZATION OF THE WILLIAMS-SYNDROME DELETION REGION ON CHROMOSOME 7Q11.23, American journal of human genetics, 61(4), 1997, pp. 204-204
HEMIZYGOTIC DELETION OF THE SYNTAXIN 1A GENE IN INDIVIDUALS WITH WILLIAMS-SYNDROME
Authors: OSBORNE LR SODER S SHI XM POBER B COSTA T SCHERER SW TSUI LC
Citation: Lr. Osborne et al., HEMIZYGOTIC DELETION OF THE SYNTAXIN 1A GENE IN INDIVIDUALS WITH WILLIAMS-SYNDROME, American journal of human genetics, 61(2), 1997, pp. 449-452
IDENTIFICATION OF GENES FROM A 500-KB REGION AT 7Q11.23 THAT IS COMMONLY DELETED IN WILLIAMS-SYNDROME PATIENTS
Authors: OSBORNE LR MARTINDALE D SCHERER SW SHI XM HUIZENGA J HENG HHQ COSTA T POBER B LEW L BRINKMAN J ROMMENS J KOOP B TSUI LC
Citation: Lr. Osborne et al., IDENTIFICATION OF GENES FROM A 500-KB REGION AT 7Q11.23 THAT IS COMMONLY DELETED IN WILLIAMS-SYNDROME PATIENTS, Genomics, 36(2), 1996, pp. 328-336
A DE-NOVO SATELLITED SHORT ARM OF THE Y-CHROMOSOME POSSIBLY RESULTINGFROM AN UNSTABLE TRANSLOCATION
Authors: LIN CL GIBSON L POBER B YANGFENG TL
Citation: Cl. Lin et al., A DE-NOVO SATELLITED SHORT ARM OF THE Y-CHROMOSOME POSSIBLY RESULTINGFROM AN UNSTABLE TRANSLOCATION, Human genetics, 96(5), 1995, pp. 585-588
PHYSICAL MAPPING OF THE 7Q11.23 REGION AND ANALYSIS OF PATIENTS WITH WILLIAMS-SYNDROME
Authors: OSBORNE LR SCHERER SW SHI XM HENG HHO COSTA T POBER B TSUI LC
Citation: Lr. Osborne et al., PHYSICAL MAPPING OF THE 7Q11.23 REGION AND ANALYSIS OF PATIENTS WITH WILLIAMS-SYNDROME, American journal of human genetics, 57(4), 1995, pp. 1549-1549
DELETION ANALYSIS OF INDIVIDUALS WITH WILLIAMS-SYNDROME AND FAMILIAL SUPRAVALVAR AORTIC-STENOSIS
Authors: SMOOT L POBER B LACRO RV KUNKEL LM
Citation: L. Smoot et al., DELETION ANALYSIS OF INDIVIDUALS WITH WILLIAMS-SYNDROME AND FAMILIAL SUPRAVALVAR AORTIC-STENOSIS, American journal of human genetics, 57(4), 1995, pp. 1572-1572
EVIDENCE FOR AN X-LINKED DISEASE LOCUS WITH A CLINICAL PHENOTYPE OF HYPOHIDROTIC ECTODERMAL DYSPLASIA AND IMMUNODEFICIENCY WITH HYPER-IGM -DISTINCT FROM BOTH THE EDA AND HIGM1 LOCI
Authors: GAULT J ORLOW S SCHNEIDER L FULEIHAN R POBER B JONES M LITT M ZONANA J
Citation: J. Gault et al., EVIDENCE FOR AN X-LINKED DISEASE LOCUS WITH A CLINICAL PHENOTYPE OF HYPOHIDROTIC ECTODERMAL DYSPLASIA AND IMMUNODEFICIENCY WITH HYPER-IGM -DISTINCT FROM BOTH THE EDA AND HIGM1 LOCI, Cytogenetics and cell genetics, 64(3-4), 1993, pp. 192-192
AN X-LINKED LOCUS WITH A PHENOTYPE OF HYPOHIDROTIC ECTODERMAL DYSPLASIA AND IMMUNODEFICIENCY WITH HYPER-IGM - APPARENTLY DISTINCT FROM BOTHTHE EDA AND HIGM1 LOCI
Authors: GAULT J ORLOW S SCHNEIDER L FULEIHAN R POBER B JONES M LITT M ZONANA J
Citation: J. Gault et al., AN X-LINKED LOCUS WITH A PHENOTYPE OF HYPOHIDROTIC ECTODERMAL DYSPLASIA AND IMMUNODEFICIENCY WITH HYPER-IGM - APPARENTLY DISTINCT FROM BOTHTHE EDA AND HIGM1 LOCI, American journal of human genetics, 53(3), 1993, pp. 1002-1002
CYTOGENETIC AND MOLECULAR CHARACTERIZATION OF A DE-NOVO SATELLITED SHORT ARM OF Y-CHROMOSOME
Authors: LIN C GIBSON L POBER B YANGFENG T
Citation: C. Lin et al., CYTOGENETIC AND MOLECULAR CHARACTERIZATION OF A DE-NOVO SATELLITED SHORT ARM OF Y-CHROMOSOME, American journal of human genetics, 53(3), 1993, pp. 1582-1582
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