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Trisomie 10 partielle par translocation familiale t(1;10) (q44;q22)

โœ Scribed by Colette Laurent; M. Bovier-Lapierre; B. Dutrillaux


Publisher
Springer
Year
1973
Tongue
English
Weight
418 KB
Volume
18
Category
Article
ISSN
0340-6717

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๐Ÿ“œ SIMILAR VOLUMES


Familial translocation t(10;21)(q22;q22)
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A family is described with a translocation t(10;21)(q22;q22) transmitted through three generations. This family was studied for the apparition of several miscarriages and two sisters with multiple malformations. Both children had a probably partial trisomy of chromosome 10 and a monosomy of chromoso

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Retardation of growth and mental development, craniofacial dysmorphy, limb anomalies, cryptorchidism and repeated infections are observed in a child with 47,XY,+der(14),t(1;14)(q44;q22)pat.

Partial trisomy of chromosome 10(q22-q24
โœ Han, J.Y. ;Kim, K.H. ;Jun, H.J. ;Je, G.H. ;Glotzbach, C.D. ;Shaffer, L.G. ๐Ÿ“‚ Article ๐Ÿ“… 2004 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 86 KB ๐Ÿ‘ 1 views

## Abstract Interchromosomal insertional translocations are rare chromosome rearrangements with an incidence of about 1:80,000 live births. We report on the clinical and cytogenetic findings of a newborn baby with partial trisomy 10q22โ€“10q24 due to a maternal insertional translocation 15;10. Partia

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A new case of partial trisomy for the long arm of chromosome 1 was observed in a newborn female, who died at age 26 days. The father was a proven carrier of a balanced translocation involving chromosomes 1 and 10.