Cytogenetic and Clinical Assessment of a Family with Treacher Collins Syndrome

Table 2

Mosaicism of deletions 5q and 3q in the affected members.

Affected members	Karyotype	%
II.2	46,XX	60
	46,XXdel(5q32-33)	30
	46,XXdel(3q23–25)	10
III.3	46,XX	53
	46,XXdel(5q32-33)	47
IV.1	46,XY	45
	46,XYdel(5q32-33)	55
IV.2	46,XX	60
	46,XXdel(5q32-33)	40