Neonatal Gorlin syndrome associated to hemimegalencephaly confirmed by genetic study [1];Síndrome de Gorlin neonatal asociado a hemimegalencefalia confirmado por estudio genético

Revista de Neurologia

Volumn 43, Issue 4, 2006, Pages 251-253

  Garcia Oguiza A ^a   Miralbes Terraza S ^a   Calvo Martin M T ^a   Labarta Aizpun, J ^a   Lopez Pison J ^a   Marco Tello, A ^a   Rebage Moisés, Victor ^a,b  

^a HOSPITAL UNIVERSITARIO MIGUEL SERVET   (Spain)

^b NONE   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

APGAR SCORE; BASAL CELL NEVUS SYNDROME; CASE REPORT; ELECTROENCEPHALOGRAPHY; FACE DYSMORPHIA; GENETIC ASSOCIATION; HUMAN; LETTER; MALE; MALFORMATION SYNDROME; MICROCEPHALY; NEWBORN; PATHOGENESIS; PHENOTYPE; VALGUS KNEE; ADULT; FEMALE; GENETICS; INFANT; MOLECULAR GENETICS; MUTATION; NERVOUS SYSTEM MALFORMATION; NUCLEOTIDE SEQUENCE; PATHOLOGY;

CELL SURFACE RECEPTOR; PATCHED RECEPTORS;

ADULT; BASAL CELL NEVUS SYNDROME; BASE SEQUENCE; FEMALE; HUMANS; INFANT; INFANT, NEWBORN; MALE; MOLECULAR SEQUENCE DATA; MUTATION; NERVOUS SYSTEM MALFORMATIONS; RECEPTORS, CELL SURFACE;

EID: 33750578443     PISSN: 02100010     EISSN: None     Source Type: Journal    
DOI: 10.33588/rn.4304.2005650     Document Type: Letter

References (17)

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