Frequency of X-chromatin or Y-chromatin positive cells in twins

Stabilized phase-shifting fringe analysis by use of current-induced frequency modulation of laser diodes.

Applied optics·2008

[Sex differences in subjective well-being and related factors in elderly people in the community aged 75 and over].

Nihon Ronen Igakkai zasshi. Japanese journal of geriatrics·2000

Mutations of a human homologue of the Drosophila eyes absent gene (EYA1) detected in patients with congenital cataracts and ocular anterior segment anomalies.

Human molecular genetics·2000

Bone metabolism after human parturition and the effect of lactation: longitudinal analysis of serum bone-related proteins and bone mineral content of the lumbar spine.

Endocrine journal·1999

No induction of chromosome aberrations in human spermatozoa exposed to extremely low frequency electromagnetic fields.

Mutation research·1998

Serum concentration of the pyridinoline cross-linked carboxyterminal telopeptide of type I collagen (ICTP) is a useful indicator of decline and recovery of bone mineral density in lumbar spine: analysis in Japanese postmenopausal women with or without hormone replacement.

Endocrine journal·1998

Gene-deletion and carrier detections, and prenatal diagnosis of Duchenne muscular dystrophy by analysis of the dystrophin gene amplified by polymerase chain reaction.

Jinrui idengaku zasshi. The Japanese journal of human genetics·1991

Rapid detection of a point mutation in thyroid-stimulating hormone beta-subunit gene causing congenital isolated thyroid-stimulating hormone deficiency.

Jinrui idengaku zasshi. The Japanese journal of human genetics·1991

Biochemical characteristics of glucose-6-phosphate dehydrogenase variants among the Malays of Singapore with report of a new non-deficient (GdSingapore) and three deficient variants.

Jinrui idengaku zasshi. The Japanese journal of human genetics·1991

Similar proportion of sporadic cases in cytochrome b558 negative chronic granulomatous disease and Duchenne muscular dystrophy.

Jinrui idengaku zasshi. The Japanese journal of human genetics·1991

The MspI restriction fragment length polymorphism of human aldolase B gene on chromosome 9q21.3-q22.2.

Jinrui idengaku zasshi. The Japanese journal of human genetics·1991

The prevalence at birth of cogenital malformations at a maternity hospital in Osaka City, 1948-1990.

Jinrui idengaku zasshi. The Japanese journal of human genetics·1991

Machine-Readable Database for Genotype-Phenotype Analyses in Rare Diseases Using FKTN-related Congenital Muscular Dystrophies as a Prototype.

Research square·2026

NEMP1 organizes the meiotic telomere LINC interface to control chromosome movement and telomere integrity.

bioRxiv : the preprint server for biology·2026

TOPBP1-Dependent DNA Damage Processing Promotes Centromere Loss in an Inviable Xenopus Hybrid.

bioRxiv : the preprint server for biology·2026

TDP-43 dysfunction induces cryptic circular RNAs in ALS/FTD.

bioRxiv : the preprint server for biology·2026

Dynamics of bleomycin-induced lung injury at single-nucleus resolution.

bioRxiv : the preprint server for biology·2026

Single-cell DNA cytometry with magnetic- and fluorescence-activated bead sorting.

bioRxiv : the preprint server for biology·2026

Related Experiment Videos

Frequency of X-chromatin or Y-chromatin positive cells in twins

Related Concept Videos

Stabilized phase-shifting fringe analysis by use of current-induced frequency modulation of laser diodes.

[Sex differences in subjective well-being and related factors in elderly people in the community aged 75 and over].

Mutations of a human homologue of the Drosophila eyes absent gene (EYA1) detected in patients with congenital cataracts and ocular anterior segment anomalies.

Bone metabolism after human parturition and the effect of lactation: longitudinal analysis of serum bone-related proteins and bone mineral content of the lumbar spine.

No induction of chromosome aberrations in human spermatozoa exposed to extremely low frequency electromagnetic fields.

Serum concentration of the pyridinoline cross-linked carboxyterminal telopeptide of type I collagen (ICTP) is a useful indicator of decline and recovery of bone mineral density in lumbar spine: analysis in Japanese postmenopausal women with or without hormone replacement.

Gene-deletion and carrier detections, and prenatal diagnosis of Duchenne muscular dystrophy by analysis of the dystrophin gene amplified by polymerase chain reaction.

Rapid detection of a point mutation in thyroid-stimulating hormone beta-subunit gene causing congenital isolated thyroid-stimulating hormone deficiency.

Biochemical characteristics of glucose-6-phosphate dehydrogenase variants among the Malays of Singapore with report of a new non-deficient (GdSingapore) and three deficient variants.

Similar proportion of sporadic cases in cytochrome b558 negative chronic granulomatous disease and Duchenne muscular dystrophy.

The MspI restriction fragment length polymorphism of human aldolase B gene on chromosome 9q21.3-q22.2.

The prevalence at birth of cogenital malformations at a maternity hospital in Osaka City, 1948-1990.

Machine-Readable Database for Genotype-Phenotype Analyses in Rare Diseases Using FKTN-related Congenital Muscular Dystrophies as a Prototype.

NEMP1 organizes the meiotic telomere LINC interface to control chromosome movement and telomere integrity.

TOPBP1-Dependent DNA Damage Processing Promotes Centromere Loss in an Inviable Xenopus Hybrid.

TDP-43 dysfunction induces cryptic circular RNAs in ALS/FTD.

Dynamics of bleomycin-induced lung injury at single-nucleus resolution.

Single-cell DNA cytometry with magnetic- and fluorescence-activated bead sorting.

Related Experiment Videos

Frequency of X-chromatin or Y-chromatin positive cells in twins

Related Concept Videos

Related Articles