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Volumn 83, Issue 5, 1999, Pages 427-429
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Oromandibular limb hypogenesis complex (Hanhart syndrome): A severe adult phenotype [3]
a
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Author keywords
[No Author keywords available]
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Indexed keywords
GROWTH FACTOR;
MORPHOGEN;
TRANSCRIPTION FACTOR;
ADULT;
CASE REPORT;
DISEASE COURSE;
DISEASE SEVERITY;
GENE MUTATION;
HUMAN;
JAW MALFORMATION;
LETTER;
LIMB MALFORMATION;
MALE;
MICROGNATHIA;
PHENOTYPE;
PRIORITY JOURNAL;
SKULL RADIOGRAPHY;
SYNDROME DELINEATION;
ABNORMALITIES, MULTIPLE;
ADULT;
HUMANS;
LIMB DEFORMITIES, CONGENITAL;
MALE;
MANDIBLE;
PHENOTYPE;
SYNDROME;
TONGUE;
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EID: 0033597186
PISSN: 01487299
EISSN: None
Source Type: Journal
DOI: 10.1002/(SICI)1096-8628(19990423)83:5<427::AID-AJMG18>3.0.CO;2-H Document Type: Letter |
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Times cited : (11)
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References (17)
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