Wolf-Hirschhorn Syndrome (WHS) - Literature review on the features of the syndrome

Advances in Clinical and Experimental Medicine

Volumn 23, Issue 3, 2014, Pages 485-489

  Paradowska Stolarz, Anna M ^a  

^a WROCLAW MEDICAL UNIVERSITY   (Poland)

Author keywords

4p16.3 deletion syndrome; Facial features; MSX1 mutation; Wolf Hirschhorn syndrome

Indexed keywords

TRANSCRIPTION FACTOR MSX1;

CHROMOSOME 4; CHROMOSOME DELETION; CLEFT LIP; CLEFT PALATE; CLINICAL FEATURE; CONGENITAL DISORDER; DECIDUOUS TOOTH; DEFORMITY; DIFFERENTIAL DIAGNOSIS; EYEBROW; FACIES; FETUS DISEASE; GENETIC ASSOCIATION; GROWTH RETARDATION; HUMAN; HYPERTELORISM; HYPODONTIA; INFANT DISEASE; MENTAL DEFICIENCY; MICROCEPHALY; MICROGNATHIA; MOLAR TOOTH; NOSE; PREMOLAR TOOTH; REVIEW; WOLF HIRSCHHORN SYNDROME; FACE MALFORMATION; OPITZ SYNDROME; PITT ROGERS DANKS SYNDROME; PRIMARY DENTITION; RUBINSTEIN SYNDROME; SMITH MAGENIS SYNDROME; TOOTH MALFORMATION;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 4; DIAGNOSIS, DIFFERENTIAL; FACE; GENETIC PREDISPOSITION TO DISEASE; GENETIC TESTING; HUMANS; MSX1 TRANSCRIPTION FACTOR; PHENOTYPE; PREDICTIVE VALUE OF TESTS; PRENATAL DIAGNOSIS; PROGNOSIS; TOOTH ABNORMALITIES; WOLF-HIRSCHHORN SYNDROME;

EID: 84905690436     PISSN: 18995276     EISSN: None     Source Type: Journal    
DOI: 10.17219/acem/24111     Document Type: Review

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