15 results on '"Dagan, Judith"'
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2. The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: Report on two patients and review of the literature
3. Whole‐genome sequencing reveals complex chromosome rearrangement disruptingNIPBLin infant with Cornelia de Lange syndrome
4. A syndrome including thumb malformations, microcephaly, short stature, and hypogonadism
5. Whole‐genome sequencing reveals complex chromosome rearrangement disrupting NIPBL in infant with Cornelia de Lange syndrome.
6. Establishment and characterization of pheochromocytoma tumor models expressing different levels of trkA receptors
7. Prenatal diagnosis of sex chromosome aneuploidy: possible reasons for high rates of pregnancy termination
8. Increased Spontaneous Chromosomal Breakage in Shwachman Syndrome
9. Transient Neonatal Diabetes mellitus in a Child with invdup(6)(q22q23) of Paternal Origin
10. t(15;21)(q15;q22.1)pat resulting in partial trisomy and partial monosomy of chromosomes 15 and 21 in two offspring
11. Paracentric inversion X(q21.2q24) associated with mental retardation in males and normal ovarian function in females
12. Simultaneous Formation of inv dup(15) and dup(15q) in a Girl with Developmental Delay: Origin of the Abnormal Chromosomes
13. Isochromosome 18p in a mother and her child
14. The ATC (ataxia-telangiectasia complementation group C) locus localizes to 11q22–q23
15. CHROMOSOMES IN ATAXIATELANGIECTASIA
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