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CHROMOSOME 9p DELETION SYNDROME

Known as: Monosomy 9p Syndrome, Chromosome 9, monosomy 9p, deletion 9p syndrome 
National Institutes of Health

Papers overview

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2006
2006
In recent years, subtelomeric rearrangements have been identified as a major cause of multiple congenital anomalies/mental… 
2004
2004
SummaryThe Miller-Dieker Syndrome (MDS) consists of lissencephaly, characteristic facies, pre- and postnatal growth retardation… 
Review
2004
Review
2004
11. Riskin-Mashiah S, Moise J, Wilkins I, Ayres N, Fraser C. In utero diagnosis of intrapericardial teratoma: a case for in utero… 
1998
1998
The insulin like growth factor 4 (INSL4) gene belongs to the insulin gene superfamily and has been mapped by fluorescent in situ… 
1990
1990
We report results of cytogenetic analysis of a cell line established from a radiation induced germ cell tumor. Tumors of this… 
1986
1986
A 26-year-old girl with multiple congenital malformations, sex-reversal, and partial trisomy 3p/monosomy 9p is described. A… 
1983
1983
A three generation pedigree is described in which there are two carriers of translocation t(7;18). Two members of the family have… 
1982
1982
The presence of a chromosomal translocation was suggested in a large kindred with several cases of mental retardation. Chromosome… 
1979
1979
A 15-month-old male with a partial monosomy 9p is reported. The comparative analysis with other cases of 9p monosomy demonstrates… 
1979
1979
A girl with a complex rearrangement of chromosome 9 is reported. She shows the characteristic clinical features of monosomy 9p…