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「"Geneix A "[Author]」の検索結果

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De novo balanced complex chromosome rearrangement (CCR) involving chromosome 8, 11 and 16 in a boy with mild developmental delay and psychotic disorder.

An unusual familial chromosome 9 "variant" with variable phenotype: characterization by CGH analysis.

Chorionic villus sampling (CVS) and fluorescence in situ hybridization (FISH) for a rapid first-trimester prenatal diagnosis.

Sperm analysis by FISH in a case of t(17; 22) (q11; q12) balanced translocation: case report.

Aspects of intracranial and spinal tumors in patients with Down syndrome and report of a rapidly progressing Grade 2 astrocytoma.

A tumor profile in Down syndrome.

Another reason to look for tumor suppressor genes on chromosome 21.

Fluorescent in-situ hybridization and sequence-tagged sites for delineation of an X:Y translocation in a patient with secondary amenorrhoea.

A history of miscarriages and mild prognathism as possible mode of presentation of mosaic trisomy 18 in women.

Hepatic calcifications in a fetus with trisomy 9 that underwent cordocentesis.

[Effect of various pharmacologic agents on the nucleus and chromosomes of human lymphocytes].

[Pericentric inversion of chromosome Y. Familial study].

47,X,i(Xq), Y karyotype. A new case.

Cytogenetic studies in a case of T-cell prolymphocytic leukemia.

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