HUMAN CHROMOSOMAL DELETION . 2 PATIENTS WITH 4P-SYNDROME

被引:35
作者
ARIAS, D
PASSARGE, E
ENGLE, MA
GERMAN, J
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D O I
10.1016/S0022-3476(70)80134-2
中图分类号
R72 [儿科学];
学科分类号
100202 ;
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页码:82 / +
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共 12 条
[1]   CHROMOSOMAL AUTORADIOGRAPHY IN CRI DU CHAT SYNDROME [J].
GERMAN, J ;
LEJEUNE, J ;
MACINTYRE, MN ;
DEGROUCH.J .
CYTOGENETICS, 1964, 3 (05) :347-+
[2]  
GERMAN J, 1967, 3 P INT C HUM GEN, P123
[3]  
Giorgi P L, 1965, Minerva Pediatr, V17, P1972
[4]  
HIRSCHHORN K, 1965, HUMANGENETIK, V1, P479
[5]  
KEMPEN CV, 1967, MAANDSCHR KINDERGENE, V35, P252
[6]  
Leao J C, 1966, Lancet, V1, P493
[7]  
LEJEUNE J, 1963, CR HEBD ACAD SCI, V257, P3098
[8]  
MILLER OJ, 1966, LANCET, V2, P105
[9]   NEW DOCUMENTS FOR DELINEATION OF A SYNDROME OF DELETION OF SHORT ARM OF ONE CHROMOSOME 4 [J].
PFEIFFER, RA .
ZEITSCHRIFT FUR KINDERHEILKUNDE, 1968, 102 (01) :49-&
[10]   FINDINGS IN PATIENT WITH APPARENT DELETION OF SHORT ARMS ON ONE OF B GROUP CHROMOSOMES [J].
SIDBURY, JB ;
GRAY, M ;
SCHMICKE.RD .
JOURNAL OF PEDIATRICS, 1964, 65 (6P2) :1098-+