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Ocular abnormalities accompanying chromosome 13 defects.
1987
M B Raizman
Associated MeSH Terms
Cite
UI
MeSH Term
Description
Entries
D007231
Infant, Newborn
An infant during the first 28 days after birth.
Neonate,Newborns,Infants, Newborn,Neonates,Newborn,Newborn Infant,Newborn Infants
D008850
Microphthalmos
Congenital or developmental anomaly in which the eyeballs are abnormally small.
Microphthalmia
D002872
Chromosome Deletion
Actual loss of portion of a chromosome.
Monosomy, Partial,Partial Monosomy,Deletion, Chromosome,Deletions, Chromosome,Monosomies, Partial,Partial Monosomies
D002882
Chromosomes, Human, Pair 13
A specific pair of GROUP D CHROMOSOMES of the human chromosome classification.
Chromosome 13
D005260
Female
Females
D006801
Humans
Members of the species Homo sapiens.
Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D012303
Ring Chromosomes
Aberrant chromosomes with no ends, i.e., circular.
Chromosomes, Ring,Chromosome, Ring,Ring Chromosome
Related Publications
M B Raizman
Ocular abnormalities in Patau syndrome (chromosome 13 trisomy syndrome).
March 1990, Ophthalmic paediatrics and genetics,
M B Raizman
Duane Retraction Syndrome and Accompanying Ocular Abnormalities.
January 2019, Beyoglu eye journal,
M B Raizman
Abnormalities of chromosome 13 in myelofibrosis.
July 1984, Scandinavian journal of haematology,
M B Raizman
Pigmentary abnormalities in trisomy of chromosome 13.
July 1998, Clinical dysmorphology,
M B Raizman
Chromosome 13 abnormalities in multiple myeloma are mostly monosomy 13.
December 2000, British journal of haematology,
M B Raizman
Clinical ocular abnormalities in infants with trisomy 13.
June 2006, American journal of ophthalmology,
M B Raizman
[Ocular abnormalities of phenotype DR (ring D chromosome)].
August 1970, Annales d'oculistique,
M B Raizman
[Abnormalities syndrome in partial trisomy of the chromosome 13].
June 1975, Hippokrates,
M B Raizman
Ocular abnormality associated with partial duplication of chromosome 13.
February 1981, Annals of ophthalmology,
M B Raizman
Ocular and cerebral abnormalities in chromosome 18 deletion defect.
September 1970, American journal of ophthalmology,
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