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Arrhinencephaly associated with a deficiency involving chromosome 18.A patient with a short arm deletion of chromosome 18 (46,XY,18p-)Absent IgA and deletions of chromosome 18Autosomal deletion syndrome 46,XX,18p-: a new case report with absence of IgA in serum.Familial reciprocal C/18 translocation.FAMILIAL SHORT ARM DEFICIENCY OF CHROMOSOME 18 CONCOMITANT WITH ARHINENCEPHALY AND ALOPECIA CONGENITAA special role of the group 17,18 chromosomes in reticuloendothelial neoplasia
P2860
Q34632913-DAED6337-B6DA-4C1B-905D-5E8253901CF3Q34633723-5604DA6F-CBCA-4145-A912-7775D15856FAQ34633908-47CC2FE6-D640-439D-8CBC-C51A23B9B90AQ34633994-7732A60F-7213-4A00-9304-2B72467A96B5Q35231401-221308E1-A97D-4655-B69D-42BD187859D5Q35913026-32D94E74-63EE-4D5C-ACB4-95DA70C56D20Q36038944-804BB69D-0424-471B-8A52-04F28696784A
P2860
description
1964 nî lūn-bûn
@nan
1964年の論文
@ja
1964年論文
@yue
1964年論文
@zh-hant
1964年論文
@zh-hk
1964年論文
@zh-mo
1964年論文
@zh-tw
1964年论文
@wuu
1964年论文
@zh
1964年论文
@zh-cn
name
PROBABLE DELETION OF THE SHORT ARM OF CHROMOSOME 18.
@ast
PROBABLE DELETION OF THE SHORT ARM OF CHROMOSOME 18.
@en
type
label
PROBABLE DELETION OF THE SHORT ARM OF CHROMOSOME 18.
@ast
PROBABLE DELETION OF THE SHORT ARM OF CHROMOSOME 18.
@en
prefLabel
PROBABLE DELETION OF THE SHORT ARM OF CHROMOSOME 18.
@ast
PROBABLE DELETION OF THE SHORT ARM OF CHROMOSOME 18.
@en
P2093
P2860
P1476
PROBABLE DELETION OF THE SHORT ARM OF CHROMOSOME 18.
@en
P2093
P2860
P304
P407
P577
1964-09-01T00:00:00Z