18q-syndrome and ectodermal dysplasia syndrome: Description of a child and his family

American Journal of Medical Genetics

Volumn 116, Issue 2, 2003, Pages 192-199

  Zannolli, R ^a   Pierluigi, M ^b   Pucci, L ^a   Lagrasta, N ^a   Gasparre, O ^a   Matera, M R ^a   Di Bartolo, R M ^a   Mazzei, M A ^a   Sacco, P ^a   Miracco, C ^a   De Santi, M M ^a   Aitiani, P ^a   Cavani, S ^a   Pellegrini, L ^a   Fimiani, M ^a   Alessandrini, C ^a   Galluzzi, P ^c   Livi, W ^a   Gonnelli, S ^a   Terrosi Vagnoli, P ^a   Zappella, M ^a   Morgese, G ^a   more..

^a UNIVERSITY OF SIENA   (Italy)

^b GALLIERA HOSPITAL   (Italy)

^c UNIVERSITY HOSPITAL OF SIENA   (Italy)

Author keywords

18q syndrome; Central nervous system; Ectodermal dysplasia syndrome

Indexed keywords

18Q SYNDROME; ARTICLE; ATTENTION DEFICIT DISORDER; AUTOSOMAL RECESSIVE DISORDER; BONE MALFORMATION; BRAIN MALFORMATION; CASE REPORT; CHROMOSOME ABERRATION; CLINICAL FEATURE; CONTROLLED STUDY; ECTODERMAL DYSPLASIA SYNDROME; FACE MALFORMATION; FAMILY; HAIR DISEASE; HEARING IMPAIRMENT; HUMAN; JOINT LAXITY; KARYOTYPE 46,XY; MALE; MENTAL DEFICIENCY; PRIORITY JOURNAL; RESTLESS LEGS SYNDROME; SCHOOL CHILD; SKIN DEFECT; SKULL MALFORMATION; SPEECH DISORDER; TIC; TONGUE DISEASE; TOOTH MALFORMATION;

EID: 12244261615     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.10069     Document Type: Article

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