Partial and complete trisomy 9: Delineation of a trisomy 9 syndrome Journal Articles

abstract

• Two infants with trisomy involving chromosome 9 are described. One had complete trisomy 9 and the other karyotype 47,XX,+der(9),t(7;9) (p22;q32)mat. A trisomy 9 syndrome is delineated, consisting of features of the trisomy 9p syndrome and various other malformations. These include abnormalities of the cardiovascular and urogenital systems, cranial suture anomalies, dislocation of the hips and knees and early death. A possible relationship of some of these findings to regions of 9q involved in cases of partial trisomy 9 is suggested.

authors

• Sutherland, Grant R
• Carter, Ronald
• Morris, Lloyd L

status

• published 

publication date

• 1976

has subject area

• 0604 Genetics (FoR)
• 1104 Complementary and Alternative Medicine (FoR)
• 1114 Paediatrics and Reproductive Medicine (FoR)
• Abnormalities, Multiple (MeSH)
• Chromosome Mapping (MeSH)
• Chromosomes, Human, 6-12 and X (MeSH)
• Female (MeSH)
• Genetics & Heredity (Science Metrix)
• Humans (MeSH)
• Infant (MeSH)
• Infant, Newborn (MeSH)
• Karyotyping (MeSH)
• Male (MeSH)
• Trisomy (MeSH)

published in

• Human Genetics  Journal

keywords

• Abnormalities, Multiple
• Chromosome Mapping
• Chromosomes, Human, 6-12 and X
• Female
• Humans
• Infant
• Infant, Newborn
• Karyotyping
• Male
• Trisomy

Digital Object Identifier (DOI)

• 10.1007/bf00291495

PubMed ID

• 1270071

start page

• 133

end page

• 140

volume

• 32

issue

• 2