Molecular genetic analysis of the 3p - syndrome

Human Molecular Genetics

Volumn 3, Issue 6, 1994, Pages 903-908

  Phipps, Maude E ^a   Latif, Farida ^a,b   Prowse, Amanda ^a   Payne, Stewart J ^a,c   Dietz band, Jeanne ^a,d   Leversha, Margaret ^a   Affara, Nabeel A ^a   Moore, Anthony T ^a,c   Tolmie, John ^a,e   Schinzel, Albert ^a,f   Lerman, Michael I ^a,b   Ferguson smith, Malcolm A ^a   Maher, Eamonn R ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b NATIONAL CANCER INSTITUTE   (United States)

^c ADDENBROOKE S HOSPITAL   (United Kingdom)

^d Oncor Inc   (United States)

^e UNIVERSITY OF GLASGOW   (United Kingdom)

^f UNIVERSITY OF ZURICH   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

DNA MARKER;

ARTICLE; CENTROMERE; CHILD; CHROMOSOME 3P; CHROMOSOME DELETION; CHROMOSOME MAP; CLINICAL ARTICLE; CONGENITAL HEART MALFORMATION; DNA DETERMINATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENETIC ANALYSIS; GROWTH RETARDATION; HEART DEVELOPMENT; HEART SEPTUM DEFECT; HUMAN; HUMAN CELL; INFANT; MALE; MENTAL DEFICIENCY; MICROCEPHALY; MICROGNATHIA; MOLECULAR GENETICS; PATHOLOGY; PATIENT CARE; PHENOTYPE; PRIORITY JOURNAL; PTOSIS; RISK FACTOR; TELOMERE; VON HIPPEL LINDAU DISEASE;

ABNORMALITIES, MULTIPLE; ADULT; CASE REPORT; CELL LINE; CHILD; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 3; FEMALE; FOLLOW-UP STUDIES; GENETIC MARKERS; HUMAN; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; LYMPHOCYTES; MALE; PHENOTYPE; POLYMORPHISM (GENETICS); SUPPORT, NON-U.S. GOV'T; SYNDROME;

EID: 0028286283     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/3.6.903     Document Type: Article

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