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. Author manuscript; available in PMC: 2017 Jul 3.
Published in final edited form as: Am J Med Genet. 1986 Mar;23(3):793–809. doi: 10.1002/ajmg.1320230307

TABLE III.

Parental Origin of Chromosome 15 Deletion

Patient
AgNOR
GTG
QFQ
No. Sex Pat Mat Child Pat Mat Child Pat Mat Child Origin
54783 F M/M L/M L/M* mp/mp sp/1p mp*/1p Pat
26676 F M/M L/S L/M* mp/mp 1p/mp 1p/mp* 4/1 3/2 2/1* Pat
54917 M M/− S/S M*/S −p+/sp −p/−p sp*/−p Pat
54101 M sp/sp mp/mp sp*/mp 2/2 3/2 3/2* Pat
23276 M M/M L/S M*/S mp/mp 1p/mp mp/mp* Pat
54573 M M/M M/− M*/− 1p/mp 1p/−p mp*/−p 3/3 2/1 3*/1 Pat
53706 M mp/mp 1p/sp 1p/mp* 1/1 3/1 3/1* Pat
54220 F 1p/1p −p+/mp 1p*/mp 4/2 1/1 4*/1 Pat
53166 M mp/sp 1p/1p 1p/sp* 3/2 5/3 5/2* Pat
29583 M mp/mp mp/mp mp/mp* 2/2 4/4 4/2* Pat
52937 M L/L M/S L*/S 1p/1p sp/sp 1p*/sp 4/2 1/1 4*/1 Pat
55274 F sp/mp sp/mp mp/sp* 4/2 3/3 3/2* Pat
55276 F mp/mp sp/sp mp*/sp 3/2 2/2 3*/2 Pat

The code for heteromorphisms described by AgNOR is: L, large; M, medium; S, small; —, inactive. GTG-stained slides were scored for satellite stalk and short arm length (I, long; m, medium; s, short; —, absent stalk; p +, long; p, normal; p, absent p arm). QFQ-stained slides were scored for satellite intensity after Paris nomenclature (1, negative; 2, pale; 3, medium; 4, intense; 5, brilliant). The deletion chromosome in each case is identified by an asterisk.