GROUP G DELETION SYNDROMES

被引:13
作者
KELCH, RP
FRANKLIN, M
SCHMICKEL, RD
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D O I
10.1136/jmg.8.3.341
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
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页码:341 / +
页数:1
相关论文
共 13 条
[1]   AUTOSOMAL MONOSOMY IN MAN - COMPLETE MONOSOMY G (21-22) IN A 4-AND-1/2-YEAR-OLD MENTALLY RETARDED GIRL [J].
ALAISH, MS ;
DELACRUZ, F ;
GOLDSMITH, LA ;
VOLPE, J ;
MELLA, G ;
ROBINSON, JC .
NEW ENGLAND JOURNAL OF MEDICINE, 1967, 277 (15) :777-+
[2]   MONOSOMY FOR A G AUTOSOME [J].
CHALLACOMBE, DN ;
TAYLOR, A .
ARCHIVES OF DISEASE IN CHILDHOOD, 1969, 44 (233) :113-+
[3]  
ENGEL E, 1966, LANCET, V1, P1130
[4]  
HALL B, 1967, HEREDITAS-GENETISK A, V57, P356
[5]   A CHILD WITH A GROUP-G RING CHROMOSOME [J].
HOEFNAGEL, D ;
SCHROEDE.M ;
BENIRSCH. .
HUMANGENETIK, 1967, 4 (01) :52-52
[6]  
LEJEUNE J, 1964, CR HEBD ACAD SCI, V259, P4187
[7]  
NEU RL, 1966, LANCET, V2, P390
[8]  
PENROSE LS, 1966, LANCET, V1, P497
[9]   A CHILD WITH PARTIAL DELETION OF A G-GROUP AUTOSOME [J].
REISMAN, LE ;
DARNELL, A ;
MURPHY, JW ;
HALL, B ;
KASAHARA, S .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1967, 114 (03) :336-&
[10]  
REISMAN LE, 1966, LANCET, V1, P394