Inherited Macrocephaly-Hamartoma syndromes

American Journal of Medical Genetics

Volumn 79, Issue 4, 1998, Pages 284-290

  DiLiberti, John H ^a  

^a UNIVERSITY OF ILLINOIS   (United States)

Author keywords

Autosomal dominant; Bannayan Riley Ruvalcaba syndrome; Carnitine; Cowden disease; Hamartoma; Lhermitte Duclos syndrome; Lipid myopathy; Macrocephaly; MATCHS; PTEN; Ruvalcaba Myhre Smith syndrome

Indexed keywords

CARNITINE; LIPID;

AUTOSOMAL DOMINANT INHERITANCE; BANNAYAN RILEY RUVALCABA SYNDROME; CANCER INCIDENCE; CHROMOSOME 10; CLINICAL FEATURE; CONFERENCE PAPER; COWDEN SYNDROME; GENE MUTATION; HAMARTOMA; HUMAN; LHERMITTE DUCLOS DISEASE; MACROCEPHALY; MULTIPLE MALFORMATION SYNDROME; MYOPATHY; ORAL DRUG ADMINISTRATION; PRIORITY JOURNAL; SKIN DISEASE; SYNDROME DELINEATION; THYROID DISEASE;

HAMARTOMA SYNDROME, MULTIPLE; HEAD; HUMANS;

EID: 0032476003     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19981002)79:4<284::AID-AJMG10>3.0.CO;2-N     Document Type: Conference Paper

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