Results 171 to 180 of about 13,528 (181)
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Stratigraphic division based on minor elements in the sediment core Q43 from the outer shelf of the East China Sea: Approached through correspondence analysis and fuzzy cluster analysis

Journal of Ocean University of China, 2005
The multivariate statistical techniques, principal component analysis, Q-mode factor analysis, correspondence analysis and fuzzy C-means clustering were applied to analyzing the datasets of minor element concentrations in sediment samples of a core collected from the outer shelf of the East China Sea.
Xiaotong Lin, Weiran Li, Shujie Du
openaire   +1 more source

Prenatal Diagnosis of a Fetus with Terminal Deletion of Chromosome 1 (q43) in First-Trimester Screening: Is There a Characteristic Antenatal 1q Deletion Phenotype? A Case Report and Review of the Literature

Fetal Diagnosis and Therapy, 2010
The terminal deletion of chromosome 1q is a disease of rare incidence. It might be hereditary or caused by spontaneous changes within the chromosome. Phenotypic characteristics including typical facial appearance, microcephaly, psychomotor retardation and variable other anomalies are suggested to be based on the loss of macrochromosomal materials ...
N, Wagner   +6 more
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A case of childhood acute myeloid leukemia AML (M5) with a neocentric chromosome neo(1)(qter-->q23 approximately 24::q23 approximately 24-->q43-->neo-->q43-->qter) and tetrasomy of chromosomes 8 and 21.

Cancer genetics and cytogenetics, 2009
Hyperdiploidy is rarely observed in childhood acute myeloid leukemia (AML). Described here is the case of a 2(1/2)-year-old girl with AML-M5 and 51 chromosomes characterized by double tetrasomy of chromosomes 8 and 21 and also a neocentric derivative chromosome neo(1)(qter-->q23 approximately 24::q23 approximately 24-->q43-->neo-->q43-->qter).
Amanda Faria, de Figueiredo   +8 more
openaire   +1 more source

MPEC 2024-Q43 : DAILY ORBIT UPDATE (2024 August 26)

The Minor Planet Electronic Circulars contain information on unusual minor planets, routine data on comets and natural satellites, and occasional editorial announcements. They are published on behalf of Division F of the International Astronomical Union by the Minor Planet Center, Smithsonian Astrophysical Observatory, Cambridge, MA 02138, U.S.A.
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Terminal (1)(q43) long-arm deletion of chromosome no. 1 in a three-year-old female.

Birth defects original article series, 1976
A 3-year-old Latin female is reported with a terminal deletion of the No. 1 chromosome, karyotype formula 46, XX, del(1) (q43). Principle clinical features include: Anatomic - microcephaly; bilateral, convergent strabismus; epicanthus; brachycephaly; bulbar nose; sparse hair; partial soft tissue syndactylism between 2nd and 3rd fingers which are ...
C B, Mankinen, J W, Sears, V R, Alvarez
openaire   +1 more source

Evidence for the assignment of GUK 1 gene locus to 1q32 leads to q43 segment from gene dosage effect.

Annales de genetique, 1980
A male infant with dup (1) (q32 leads to q43) constitution is reported. He had mental and physical retardation and a constellation of dysmorphisms, which are considered characteristic of trisomics for the distal one-third of the long arm of chromosome 1.
B, Dallapiccola   +4 more
openaire   +1 more source

Distal deletion of the long arm of chromosome number 1 (q43-->qter) associated with severe mental retardation and a nonspecific dysmorphic syndrome.

Annales de genetique, 1993
A 6 8/12-year-old girl with severe mental retardation, multiple congenital malformations and a de novo distal deletion of the long arm of chromosome 1 [del 1 (q43-->qter)] is here described. A review of the reported patients does not allow to distinguish different phenotypes related to distal deletion 1q42 and/or 1q43.
D M, Ioan   +3 more
openaire   +1 more source

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