CHROMOSOME 9p DELETION SYNDROME

Known as: Monosomy 9p Syndrome, Chromosome 9, monosomy 9p, deletion 9p syndrome 
 

Topic mentions per year

Topic mentions per year

1976-2015
012319762015

Papers overview

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2013
2013
A 4-month-old Sri Lankan male child case with a de novo terminal deletion in the p22→pter region of chromosome 9 is described… (More)
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2011
2011
We report on a 17-year-old patient with midline defects, ocular hypertelorism, neuropsychomotor development delay, neonatal… (More)
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2011
2011
Monosomy 9p syndrome, also known as Alfi syndrome, has been described as a contiguous syndrome characterized by mental… (More)
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2009
2009
We read the manuscript by Swinkels et al. [2008], ‘‘Clinical and Cytogenetic Characterization of 13 Dutch Patients With Deletion… (More)
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1999
1999
A male infant with a deletion of 9p and concomitant duplication of 4q: 46,XY, der(9)t(4;9)(q27;p24), is described. Parental… (More)
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1995
1995
A child with phenotypic features of the 9p- syndrome, including metopic craniosynostosis, small ears, abdominal wall defect, and… (More)
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1989
1989
We describe a newborn infant with 9p- syndrome and nonketotic hyperglycinemia. This unusual occurrence may not have been… (More)
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1985
1985
This report describes an adult male with a partial trisomy 6p(p211-pter) and a partial monosomy 9p(9p24-pter) resulting from a de… (More)
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1976
1976
Six patients (4 females and 2 males) with terminal deletion of the short arm of chromosome 9 distal to band p22 are described… (More)
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