Monosomy 1p36

Journal of Medical Genetics

Volumn 36, Issue 9, 1999, Pages 657-663

  Slavotinek, Anne ^a,c   Shaffer, Lisa G ^b   Shapira, Stuart K ^b  

^a ST MARY S HOSPITAL   (United Kingdom)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

^c NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

Author keywords

Contiguous gene deletion syndrome; Monosomy 1p36

Indexed keywords

ADOLESCENT; ANTERIOR FONTANEL; CARDIOMYOPATHY; CHILD; CHROMOSOME 1P; CLINICAL ARTICLE; CRANIOFACIAL MALFORMATION; DEVELOPMENTAL DISORDER; FEMALE; FOREHEAD; GENE DELETION; GROWTH RETARDATION; HUMAN; INFANT; MALE; MICROCEPHALY; MIDFACE HYPOPLASIA; MONOSOMY; MUSCLE HYPOTONIA; NEWBORN; PERCEPTION DEAFNESS; PRIORITY JOURNAL; REVIEW;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 1; FEMALE; HUMANS; INFANT; INFANT, NEWBORN; MALE; MIDDLE AGED; SYNDROME;

EID: 0032884027     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

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