Chromosome 7 short arm deletion and craniosynostosis. A 7p-syndrome

Chromosome 7 short arm deletion and craniosynostosis. A 7p-syndrome

A patient with craniosynostosis and a small deletion of part of the short arm of chromosome 7 is described. A review of the literature indicates that craniosynostosis has occurred in at least four of the five infants (the fifth having microcephaly) affected by structural changes (resulting in deleti...

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Veröffentlicht in:Human genetics 1976-01, Vol.35 (1), p.117-123
Hauptverfasser: Gong, B T, Norwood, T H, Hoehn, H, McPherson, E, Hall, J G, Hickman, R
Format: Artikel
Sprache:eng
Schlagworte:
Blood Group Antigens
Chromosome Aberrations
Chromosome Deletion
Chromosomes, Human, 6-12 and X
Craniosynostoses - diagnosis
Craniosynostoses - genetics
Dermatoglyphics
Enzymes - blood
Humans
Infant, Newborn
Karyotyping
Male
Pedigree
Phenotype
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Beschreibung
Zusammenfassung:A patient with craniosynostosis and a small deletion of part of the short arm of chromosome 7 is described. A review of the literature indicates that craniosynostosis has occurred in at least four of the five infants (the fifth having microcephaly) affected by structural changes (resulting in deletion) within the terminal region of the short arm of chromosome 7.
ISSN:0340-6717
1432-1203
DOI:10.1007/BF00295627