On the association profound nerve deafness, semilobar holoprosencephaly, and minor midline developmental anomalies

Genetic Counseling

Volumn 10, Issue 4, 1999, Pages 399-401

  Vantrappen, Greet ^a   Feenstra, L ^b   Fryns, J P ^b  

^a UNIVERSITY HOSPITALS LEUVEN   (Belgium)

^b NONE

Author keywords

Deafness; Holoprosencephaly; Midline developmental defects

Indexed keywords

ARTICLE; CASE REPORT; DEVELOPMENTAL DISORDER; DISEASE ASSOCIATION; HOLOPROSENCEPHALY; HUMAN; HUMAN CELL; MALE; PERCEPTION DEAFNESS; PRESCHOOL CHILD;

ABNORMALITIES, MULTIPLE; DEAFNESS; GENITALIA, MALE; HOLOPROSENCEPHALY; HUMANS; INFANT; KARYOTYPING; MALE; SYNDROME;

EID: 0033405451     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (1)

1. MÜNCKE M.: Clinical, cytogenetic and molecular approaches to the genetic heterogeneity of holoprosencephaly. Am. J. Med. Genet., 1989, 34, 237-245.