Cryptic pericentric inversion of chromosome 17 detected by fluorescence in situ hybridization study in familial Miller-Dieker syndrome.

American journal of medical genetics

Volumn 71, Issue 2, 1997, Pages 236-237

  Yokoyama, Y ^a   Narahara, K ^a   Teraoka, M ^a   Koyama, K ^a   Seino, Y ^a   Yagi, S ^a   Konishi, T ^a   Miyawaki, T ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CHROMOSOME 17; CHROMOSOME INVERSION; CRANIOFACIAL MALFORMATION; FLUORESCENCE IN SITU HYBRIDIZATION; GENETICS; HUMAN; INFANT; MALE; MULTIPLE MALFORMATION SYNDROME; NOTE; PEDIGREE; SYNDROME; ULTRASTRUCTURE;

ABNORMALITIES, MULTIPLE; CHROMOSOMES, HUMAN, PAIR 17; CRANIOFACIAL ABNORMALITIES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INVERSION, CHROMOSOME; MALE; PEDIGREE; SYNDROME;

EID: 0031559410     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970808)71:2<236::AID-AJMG24>3.0.CO;2-E     Document Type: Note

References (0)