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6 in total

1. Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance.

Authors: J C Barber; C A Joyce; M N Collinson; J C Nicholson; L R Willatt; H M Dyson; M S Bateman; A J Green; J R Yates; N R Dennis
Journal: J Med Genet Date: 1998-06 Impact factor: 6.318

2. Inherited interstitial duplications of proximal 15q: genotype-phenotype correlations.

Authors: C E Browne; N R Dennis; E Maher; F L Long; J C Nicholson; J Sillibourne; J C Barber
Journal: Am J Hum Genet Date: 1997-12 Impact factor: 11.025

3. Organisation of the pericentromeric region of chromosome 15: at least four partial gene copies are amplified in patients with a proximal duplication of 15q.

Authors: J A Fantes; S K Mewborn; C M Lese; J Hedrick; R L Brown; V Dyomin; R S K Chaganti; S L Christian; D H Ledbetter
Journal: J Med Genet Date: 2002-03 Impact factor: 6.318

Review 4. Directly transmitted unbalanced chromosome abnormalities and euchromatic variants.

Authors: J C K Barber
Journal: J Med Genet Date: 2005-08 Impact factor: 6.318

5. Prenatal diagnosis and genetic counseling of a paternally inherited microduplication 18q11.1 to 18q11.2 in a chinese family.

Authors: Juan Chen; Ying Zhang; Mingxi Zhang
Journal: Mol Cytogenet Date: 2022-09-01 Impact factor: 1.904

6. Familial microdeletion 18p11.32 to 18p11.31 in a Chinese family with normal phenotype.

Authors: Miaomiao Han; Lei Wei; Fang Liu; Xia Gao
Journal: Mol Cytogenet Date: 2022-03-24 Impact factor: 2.009

6 in total