A FURTHER CASE OF TERMINAL DELETION (14)(Q32.2) IN A CHILD WITH MILD DYSMORPHIC FEATURES

被引：0

作者：

WANG, HS ^{[1
]}

ALLANSON, JE ^{[1
]}

机构：

[1] CHILDRENS HOSP EASTERN ONTARIO,DIV GENET,401 SMYTH RD,OTTAWA K1H 8L1,ONTARIO,CANADA

来源：

ANNALES DE GENETIQUE | 1992年 / 35卷 / 03期

关键词：

CHROMOSOME-14; DELETION; DYSMORPHISM;

D O I：

暂无

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

The fifth patient with a terminal deletion of the long arm of chromosome 14 is reported, and compared with previous cases.

引用

页码：171 / 173

页数：3

共 6 条

[1]

ANYADIKE IO, 1991, C J DIAGN, P39

[2] DISTAL MONOSOMY-14 NOT ASSOCIATED WITH RING FORMATION [J].

HREIDARSSON, SJ ;

STAMBERG, J .

JOURNAL OF MEDICAL GENETICS, 1983, 20 (02) :147-149

[3] RING CHROMOSOME 14 - A DISTINCT CLINICAL ENTITY [J].

SCHMIDT, R ;

EVIATAR, L ;

NITOWSKY, HM ;

WONG, M ;

MIRANDA, S .

JOURNAL OF MEDICAL GENETICS, 1981, 18 (04) :304-307

[4] TERMINAL DELETION (14)(Q32.3) - A NEW CASE [J].

TELFORD, N ;

THOMSON, DAG ;

GRIFFITHS, MJ ;

ILETT, S ;

WATT, JL .

JOURNAL OF MEDICAL GENETICS, 1990, 27 (04) :261-263

[5]

TURLEAU C, 1984, ANN GENET-PARIS, V27, P237

[6] A TERMINAL DELETION (14)(Q31.1) IN A CHILD WITH MICROCEPHALY, NARROW PALATE, GINGIVAL HYPERTROPHY, PROTUBERANT EARS, AND MILD MENTAL-RETARDATION [J].

YEN, FS ;

PODRUCH, PE ;

WEISSKOPF, B .

JOURNAL OF MEDICAL GENETICS, 1989, 26 (02) :130-133

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