Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome

American Journal of Human Genetics

Volumn 72, Issue 5, 2003, Pages 1200-1212

  Heilstedt, Heidi A ^a   Ballif, Blake C ^a   Howard, Leslie A ^a   Lewis, Richard A ^a   Stal, Samuel ^a   Kashork, Catherine D ^a   Bacino, Carlos A ^a   Shapira, Stuart K ^b   Shaffer, Lisa G ^a,c  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b University of Texas Health Science Center   (United States)

^c WASHINGTON STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CONTIG;

ARTICLE; CARDIOVASCULAR MALFORMATION; CHILD; CHROMOSOME 1P; CHROMOSOME DELETION; CHROMOSOME MAP; CHROMOSOME REARRANGEMENT; CLUSTER ANALYSIS; CONTROLLED STUDY; CRANIOFACIAL MALFORMATION; EXTRACHROMOSOMAL INHERITANCE; EYE MALFORMATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENETIC ANALYSIS; GENOTYPE PHENOTYPE CORRELATION; HEARING LOSS; HUMAN; HUMAN CELL; INFANT; MAJOR CLINICAL STUDY; MALE; MOLECULAR ANALYSIS; MONOSOMY; MONOSOMY 1P; NEUROLOGIC DISEASE; NEWBORN; PRIORITY JOURNAL;

EID: 0038406165     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/375179     Document Type: Article

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