Petty syndrome and fontaine-farriaux syndrome: Delineation of a single syndrome

American Journal of Medical Genetics, Part A

Volumn 152, Issue 7, 2010, Pages 1718-1723

  Braddock, Stephen R ^a   Ardinger, Holly H ^b   Yang, Chun Song ^c   Paschal, Bryce M ^c   Hall, Bryan D ^d  

^a UNIVERSITY OF VIRGINIA HEALTH SYSTEM   (United States)

^b CHILDREN S MERCY HOSPITAL   (United States)

^c UNIVERSITY OF VIRGINIA   (United States)

^d UNIVERSITY OF KENTUCKY   (United States)

Author keywords

Craniosynostosis; Fontaine Farriaux syndrome; Laminopathy; Lipodystrophy; Nail hypoplasia; Petty syndrome; Progeria

Indexed keywords

LAMIN A; LAMIN C;

ANAMNESIS; ARTICLE; CHILD; CLINICAL FEATURE; CONGENITAL DISORDER; CONTROLLED STUDY; FEMALE; FONTAINE FARRIAUX SYNDROME; GENE; GENETIC DISORDER; HUMAN; KARYOTYPE; MALE; PETTY SYNDROME; PHENOTYPE; PRIORITY JOURNAL; ABNORMALITIES, MULTIPLE; CASE REPORT; CELL NUCLEUS; FACIES; FATALITY; INFANT; NEWBORN; PREGNANCY; SYNDROME; ULTRASTRUCTURE;

ABNORMALITIES, MULTIPLE; CELL NUCLEUS; FACIES; FATAL OUTCOME; FEMALE; HUMANS; INFANT; INFANT, NEWBORN; MALE; PREGNANCY; SYNDROME;

EID: 77954126142     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.33468     Document Type: Article

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