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1 . Academic Journal
Replicative senescence in organ transplantation—mechanisms and significance
저자
by
Chkhotua, A
;
Shohat, M
;
Tobar, A
;
Magal, N
;
Kaganovski, E
, et al.
소스
In
Transplant Immunology
2002 9(2):165-171
Full Text (ScienceDirect)
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7 . Academic Journal
High frequency of autosomal-recessive DFNB59 hearing loss in an isolated Arab population in Israel
저자
by
Borck, G
;
Rainshtein, L
;
Hellman-Aharony, S
;
Volk, AE
;
Friedrich, K
, et al.
소스
Clinical Genetics
. Sep 01, 2012 82(3):271-276
Web of Science
Scopus
JCR 저널정보
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7 . Academic Journal
Infantile bilateral striatal necrosis maps to chromosome 19q.
저자
by
Basel-Vanagaite, L
;
Straussberg, R
;
Ovadia, H
;
Kaplan, A
;
Magal, N
, et al.
소스
Neurology; 2004 Jan 13, Vol. 62 Issue 1, p87-90, 4p
Full Text (LWW)
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7 . Academic Journal
Overexpression of a set of genes, including WISP-1, common to pulmonary metastases of both mouse D122 Lewis lung carcinoma and B16-F10.9 melanoma cell lines.
저자
by
Margalit, O
;
Eisenbach, L
;
Amariglio, N
;
Kaminski, N
;
Harmelin, A
, et al.
소스
British Journal of Cancer
. 7/21/2003, Vol. 89 Issue 2, p314-319. 6p.
Web of Science
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7 . Academic Journal
Facial clefting in an Arab town in Israel.
저자
by
Jaber, L
;
Nahmani, A
;
Halpern, GJ
;
Shohat, M
.
소스
Clinical Genetics
. Jun2002, Vol. 61 Issue 6, p448-453. 6p.
Web of Science
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6 . Academic Journal
Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
저자
by
Avrahami, L
;
Maas, S
;
Pasmanik-Chor, M
;
Rainshtein, L
;
Magal, N
, et al.
소스
Clinical Genetics
. Jul 01, 2008 74(1):47-53
Web of Science
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7 . Academic Journal
Higher than expected carrier rates for familial Mediterranean fever in various Jewish ethnic groups.
저자
by
Stoffman, N
;
Magal, N
;
Shohat, T
;
Lotan, R
;
Koman, S
, et al.
소스
European Journal of Human Genetics
. Apr2000, Vol. 8 Issue 4, p307. 4p.
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7 . Academic Journal
Expanding the phenotypic spectrum of L1CAM-associated disease
저자
by
Basel-Vanagaite, L
;
Straussberg, R
;
Friez, M J
;
Inbar, D
;
Korenreich, L
, et al.
소스
Clinical Genetics
. May 01, 2006 69(5):414-419
Web of Science
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7 . Academic Journal
The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation
저자
by
Basel-Vanagaite, L
;
Attia, R
;
Yahav, M
;
Ferland, R J
;
Anteki, L
, et al.
소스
JOURNAL OF MEDICAL GENETICS
. Mar 01, 2006 43(3):203-210
Full Text (BMJ Journals)
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7 . Academic Journal
A putative new locus for an autosomal recessive cerebellar ataxia syndrome on chromosome 22q11
저자
by
Baris, H
;
Legum, C
;
Levin, L
;
Magal, N
;
Drasinover, V
, et al.
소스
Clinical Genetics
. Aug 01, 2005 68(2):185-187
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