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مقالات الدوريات
3
0
Molecular analysis of berardinelli-seip congenital lipodystrophy in Oman : evidence for multiple loci.
Heathcote, Kirsten.
American Diabetes Association Inc.
2002-05-01
Molecular analysis of berardinelli-seip congenital lipodystrophy in Oman : evidence for multiple loci.
مقالات الدوريات
0
0
Fatal cardiac arrhythmia and long-qt syndrome in a new form of congenital generalized lipodystrophy with muscle rippling (cgl4) due to ptrf-cavin mutations.
Rajab, Anna.
Elsevier B. V.
2010-03
Fatal cardiac arrhythmia and long-qt syndrome in a new form of congenital generalized lipodystrophy with muscle rippling (cgl4) due to ptrf-cavin mutations.
مقالات الدوريات
0
0
Recessive developmental delay, small stature, microcephaly and brain calcifications with locus on chromosome 2.
Rajab, Anna.
Elsevier B. V.
2009-02
Recessive developmental delay, small stature, microcephaly and brain calcifications with locus on chromosome 2.
مقالات الدوريات
0
0
Developmental and degenerative features in a complicated spastic paraplegia.
Manzini, M. Chiara.
Wiley.
2010-04
Developmental and degenerative features in a complicated spastic paraplegia.
مقالات الدوريات
0
0
Genetic services and testing in the Sultanate of Oman : Sultanate of Oman steps into modern genetics.
Rajab, Anna.
Elsevier.
2013-07
Genetic services and testing in the Sultanate of Oman : Sultanate of Oman steps into modern genetics.
مقالات الدوريات
0
0
Loss of PCLO function underlies pontocerebellar hypoplasia type III.
Ahmed, Mustafa Y.
Lippincott Williams and Wilkins.
2015-04
Loss of PCLO function underlies pontocerebellar hypoplasia type III.
مقالات الدوريات
0
0
Cytogenetic studies in couples with recurrent miscarriage in the Sultanate of Oman.
Goud, Tadakal Mallana.
Reproductive Healthcare.
2009-03
Cytogenetic studies in couples with recurrent miscarriage in the Sultanate of Oman.
مقالات الدوريات
0
0
Cytogenetic studies of 1232 patients with different sexual development abnormalities from the Sultanate of Oman.
Al-Alawiyah, Intisar.
Elsevier.
2016-02
Cytogenetic studies of 1232 patients with different sexual development abnormalities from the Sultanate of Oman.
مقالات الدوريات
0
0
Repository of mutations from Oman : the entry point to a national mutation database [version 1; referees : 2 approved].
Rajab, Anna.
F1000 Research.
2015-09
Repository of mutations from Oman : the entry point to a national mutation database [version 1; referees : 2 approved].
مقالات الدوريات
0
0
Importance of FISH combined with morphology, immunophenotype and cytogenetic analysis of childhood/adult acute lymphoblastic leukemia in Omani patients.
Goud, Tadakal Mallana.
Asian Pacific Organization for Cancer Prevention.
2015-12
Importance of FISH combined with morphology, immunophenotype and cytogenetic analysis of childhood/adult acute lymphoblastic leukemia in Omani patients.
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Human chromosome abnormalities--Diagnosis--Oman
(2)
Cerebellar diseases--Oman
(1)
Chromosome abnormalities--Oman
(1)
Codon, Nonsense--Oman
(1)
Cytogenetic analysis--Oman
(1)
Cytogenetics--Oman
(1)
Fetus--Abnormalities--Oman
(1)
Genetic disorders--Oman
(1)
Genetic linkage--Oman
(1)
Heart--Pathophysiology--Oman
(1)
Human genetics--Variation--Oman
(1)
Klinefelter's syndrome--Oman
(1)
Leukemia--Oman
(1)
Long QT syndrome--Oman
(1)
Miscarriage--Oman
(1)
Nervous system--Diseases--Oman
(1)
Oman--Population
(1)
Population genetics--Oman
(1)
Sex chromosome abnormalities--Oman
(1)
المؤلف
Rajab, Anna.
(4)
Goud, Tadakal Mallana.
(2)
Ahmed, Mustafa Y.
(1)
Al-Alawiyah, Intisar.
(1)
Heathcote, Kirsten.
(1)
Manzini, M. Chiara.
(1)
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Elsevier
(2)
Elsevier B V
(2)
American Diabetes Association Inc
(1)
Asian Pacific Organization for Cancer Prevention
(1)
F1000 Research
(1)
Lippincott Williams and Wilkins
(1)
Reproductive Healthcare
(1)
Wiley
(1)
sfy39587stp18
