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FAMILIAL SHORT ARM DEFICIENCY OF CHROMOSOME 18 CONCOMITANT WITH ARHINENCEPHALY AND ALOPECIA CONGENITA.

作者信息

UCHIDA I A, MCRAE K N, RAY M

出版信息

Am J Hum Genet. 1965 Sep;17(5):410-9.

Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef12/1932656/66cd75f6d981/ajhg00545-0041-a.jpg

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[Deletion of the short arms of chromosome No. 18].
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A patient with a short arm deletion of chromosome 18 (46,XY,18p-).
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Arrhinencephaly associated with a deficiency involving chromosome 18.
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Deletion of short arm of a chromosome 18 (46, XX, 18 p-).
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本文引用的文献

1
DELETION OF THE SHORT ARM OF CHROMOSOME 18.
Cytogenetics. 1964;3:201-6. doi: 10.1159/000129811.
2
PROBABLE DELETION OF THE SHORT ARM OF CHROMOSOME 18.
Am J Hum Genet. 1964 Sep;16(3):364-74.
3
[3 CASES OF PARTIAL DELETION OF THE SHORT ARM OF A 5 CHROMOSOME].
C R Hebd Seances Acad Sci. 1963 Nov 18;257:3098-102.
5
Arhinencephaly.
J Pediatr. 1963 Jun;62:895-900. doi: 10.1016/s0022-3476(63)80104-3.
6
Cebocephaly with endocrine dysgenesis. Report of 3 cases.
J Pediatr. 1961 Nov;59:726-33. doi: 10.1016/s0022-3476(61)80010-3.

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