Diagnosis of FS should not be made until PKS is ruled out [2] (multiple letters)

American Journal of Medical Genetics

Volumn 102, Issue 3, 2001, Pages 306-

  Zenker, Martin ^a,b   Vargas, Juan ^c   Cox, Gerald F ^c   Korf, Bruce R ^c  

^a UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

^b UNIVERSITY HOSPITAL ERLANGEN   (Germany)

^c HARVARD INSTITUTES OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 12P; CHROMOSOME MOSAICISM; CYTOGENETICS; DIFFERENTIAL DIAGNOSIS; FAMILIAL DISEASE; FLUORESCENCE IN SITU HYBRIDIZATION; FRYNS SYNDROME; HUMAN; ISOCHROMOSOME; LETTER; MONOZYGOTIC TWINS; PALLISTER KILLIAN SYNDROME; PRIORITY JOURNAL; SUPERNUMERARY CHROMOSOME;

EID: 0035882386     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.1447     Document Type: Letter

References (0)