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مکتبة رقمیه للعلوم الطبيه
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Results of search for 'au:"Abu, Almogit"'
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Authors
Abu, Almogit
Aviram-Goldring, Ayala
Avni, Isaac
Ben-Amitai, Dan
Berkun, Yackov
Frydman, Moshe
Gerad, Liora
Horev, Liran
Ingber, Arieh
Livneh, Avi
Marek, Dina
Marek-Yagel, Dina
Morad, Yair
Nir, Uri
Padeh, Shai
Pras, Elon
Pras, Eran
Pras, Mordechai
Reish, Orit
Reznik-Wolf, Haike
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Topics
AC133 Antigen
Adolescent
Adult
Alleles
Antigens, CD
Base Sequence
Child
Child, Preschool
Chromosome Mapping
Corneal Diseases
Female
Frameshift Mutation
Haplotypes
Humans
Male
Mutation
Pedigree
Syndrome
Young Adult
genetics
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English
Your search returned 5 results.
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1.
Deleterious mutations in the Zinc-Finger 469 gene cause brittle cornea syndrome.
[electronic resource]
by
Abu, Almogit
Frydman, Moshe
Marek, Dina
Pras, Eran
Nir, Uri
Reznik-Wolf, Haike
Pras, Elon
Producer:
20080716
In:
American journal of human genetics
vol. 82
Online resources:
Available from publisher's website
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No items available.
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2.
Cone-rod dystrophy and a frameshift mutation in the PROM1 gene.
[electronic resource]
by
Pras, Eran
Abu, Almogit
Rotenstreich, Ygal
Avni, Isaac
Reish, Orit
Morad, Yair
Reznik-Wolf, Haike
Pras, Elon
Producer:
20091028
In:
Molecular vision
vol. 15
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No items available.
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3.
Clinical disease among patients heterozygous for familial Mediterranean fever.
[electronic resource]
by
Marek-Yagel, Dina
Berkun, Yackov
Padeh, Shai
Abu, Almogit
Reznik-Wolf, Haike
Livneh, Avi
Pras, Mordechai
Pras, Elon
Producer:
20090817
In:
Arthritis and rheumatism
vol. 60
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Available from publisher's website
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No items available.
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4.
Mapping of a gene causing brittle cornea syndrome in Tunisian jews to 16q24.
[electronic resource]
by
Abu, Almogit
Frydman, Moshe
Marek, Dina
Pras, Eran
Stolovitch, Chaim
Aviram-Goldring, Ayala
Rienstein, Shlomit
Reznik-Wolf, Haike
Pras, Elon
Producer:
20070201
In:
Investigative ophthalmology & visual science
vol. 47
Online resources:
Available from publisher's website
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No items available.
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5.
An autosomal recessive form of monilethrix is caused by mutations in DSG4: clinical overlap with localized autosomal recessive hypotrichosis.
[electronic resource]
by
Zlotogorski, Abraham
Marek, Dina
Horev, Liran
Abu, Almogit
Ben-Amitai, Dan
Gerad, Liora
Ingber, Arieh
Frydman, Moshe
Reznik-Wolf, Haike
Vardy, Daniel A
Pras, Elon
Producer:
20060705
In:
The Journal of investigative dermatology
vol. 126
Online resources:
Available from publisher's website
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