15 results on '"Maya, Idit"'
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2. Exploring inheritance, and clinical penetrance of distal Xq28 duplication syndrome: insights from 47 new unpublished cases
3. Prenatal and postnatal chromosomal microarray analysis in 885 cases of various congenital heart defects
4. The effect of polyhydramnios degree on chromosomal microarray results: a retrospective cohort analysis of 742 singleton pregnancies
5. Is it time to report carrier state for recessive disorders in every microarray analysis?—A pilot model based on hearing loss genes deletions
6. A study of normal copy number variations in Israeli population
7. Chromosomal microarray should be performed for cases of fetal short long bones detected prenatally
8. Teaching clinicians practical genomic medicine: 7 years’ experience in a tertiary care center
9. Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies
10. The rare 13q33–q34 microdeletions: eight new patients and review of the literature
11. Noncoding copy-number variations are associated with congenital limb malformation
12. Prenatal microarray analysis in right aortic arch—a retrospective cohort study and review of the literature
13. Microarray analysis in pregnancies with isolated unilateral kidney agenesis
14. High-frequency low-penetrance copy-number variant classification: should we revise the existing guidelines?
15. Homozygous MED25 mutation implicated in eye–intellectual disability syndrome
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