TERTIARY PARTIAL 14 TRISOMY 47,XX,+14Q-

被引：28

作者：

FRYNS, JP

CASSIMAN, JJ

VANDENBE.H

机构：

[1] UNIV LEUVEN, DEPT PEDIAT, LEUVEN, BELGIUM

[2] UNIV LEUVEN, DEPT HUMAN BIOL, DIV HUMAN GENET, LEUVEN, BELGIUM

来源：

HUMANGENETIK | 1974年 / 24卷 / 01期

关键词：

D O I：

10.1007/BF00281111

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：71 / 77

页数：7

共 24 条

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[2]

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[3] INHERITED SMALL EXTRA CHROMOSOME - MOTHER WITH 46,XX,T(17-22)(PL-QL) AND A SON WITH 47,XY, +DER(22) MAT [J].

BORGAONKAR, DS ;

MCKUSICK, VA ;

FARBER, PA .

JOURNAL OF MEDICAL GENETICS, 1973, 10 (04) :379-384

[4] QUINACRINE FLUORESCENCE FOR IDENTIFYING METAPHASE CHROMOSOMES, WITH SPECIAL REFERENCE TO PHOTOMICROGRAPHY [J].

BREG, WR .

STAIN TECHNOLOGY, 1972, 47 (02) :87-&

[5] SEGREGATING RECIPROCAL (4-21) (Q21-Q21) TRANSLOCATION WITH PROPOSITA TRISOMIC FOR PARTS OF 4Q AND 21 [J].

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KOIVISTO, M ;

SCHRODER, J .

JOURNAL OF MEDICAL GENETICS, 1973, 10 (04) :384-389

[6]

ENDO A, 1972, JPN J HUM GENET, V17, P44

[7] NEWBORN WITH CAT-EYE SYNDROME [J].

FRYNS, JP ;

VANDENBE.H ;

VERRESEN, H ;

EGGERMONT, E .

HUMANGENETIK, 1972, 15 (03) :242-+

[8]

GERALD PS, 1968, PEDIATR RES, V2, P297

[9] SIBLINGS WITH DIFFERENT TYPES OF CHROMOSAL ABERRATIONS DUE TO D/E-TRANSLOCATION OF MOTHER [J].

HAUSCHTE.E ;

MURSET, G ;

PRADER, A ;

BUHLER, E .

CYTOGENETICS, 1966, 5 (05) :281-&

[10]

JACOBS PA, 1972, 4 P INT C HUM GEN, P242

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