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CHROMOSOME 9p DELETION SYNDROME

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

Related topics

Related topics

21 relations
9p partial monosomy syndromeAtrial Septal DefectsAutosomal dominant inheritanceChoanal Atresia

Broader (2)

Chromosome DeletionChromosomes, Human, Pair 9

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2008
2008
Mechanisms in disorders of sex development
“Is it a boy or a girl?” This is usually the first question that parents have when their baby is born. Sometimes it is not… 
2004
2004
[Diagnosis of 9p- syndrome at birth. A new case].
2003
2003
Monosomy 18p due to whole arm translocation
Monosomy 18p is one of the most frequent autosomal deletion syndrome, with variable clinical presentation. Most cases are due to… 
2001
2001
[Monosomy r(13), a new observation].
2001
2001
Ring 13 chromosome
1993
1993
10p monosomy, a phenotypic variant.
1980
1980
Two new cases of 9p- syndrome
Two new cases of 9p- syndrome are presented. Two girls have the monosomy of 9p with several clinical features typical for this… 
1979
1979
Type and contretype signs in monosomy and trisomy 9p. On a case 46,XY, del (9) (pter yields p12:).
A 15-month-old male with a partial monosomy 9p is reported. The comparative analysis with other cases of 9p monosomy demonstrates… 
1979
1979
Is it G banding sufficient for the localization of breakpoints in translocations?
The authors of the paper cited above reported a case of (13q; 18q)(q 12;q23) translocation with proximal 13q monosomy. With the… 
1977
1977
A case of 9p- syndrome
SummaryAn 8-month-old female child with the 9p- karyotype: 46,XX,del(9) (p22) is presented, being the first case from among…