Another explanation for familial Cornelia de Lange syndrome [2]

American Journal of Medical Genetics

Volumn 118 A, Issue 2, 2003, Pages 198-

  Gardner, R J M ^a  

^a ROYAL CHILDREN'S HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

AUTISM; AUTOSOMAL DOMINANT INHERITANCE; CHILD; DE LANGE SYNDROME; GENE MUTATION; GENETIC MODEL; HUMAN; LETTER; PRIORITY JOURNAL; SYNDROME DELINEATION; DOMINANT GENE; FAMILY HEALTH; GENETICS; MULTIFACTORIAL INHERITANCE; NOTE; PATHOLOGY;

DE LANGE SYNDROME; FAMILY HEALTH; GENES, DOMINANT; HUMANS; MULTIFACTORIAL INHERITANCE;

EID: 0041319489     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (2)

1. Li CC. 1987. A genetical model for emergenesis: In memory of Laurence H. Snyder, 1901-86. Am J Hum Genet 41:517-523.
2. Russell KL, Ming JE, Patel K, Jukofsky L, Magnusson M, Krantz ID. 2001. Dominant paternal transmission of Cornelia de Lange syndrome: A new case and review of 25 previously reported familial recurrences. Am J Med Genet 104:267-276.