A cytogenetic survey of consecutive liveborn infants-incidence and type of chromosome abnormalities

Long waiting time before tooth extraction may increase delayed wound healing in elderly Japanese.

Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA·2018

Issues with the surgical treatment of antiresorptive agent-related osteonecrosis of the jaws.

Oral diseases·2018

Significant improvement of bone mineral density and bone turnover markers by denosumab therapy in bisphosphonate-unresponsive patients.

Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA·2016

Efficacy and safety of once-yearly zoledronic acid in Japanese patients with primary osteoporosis: two-year results from a randomized placebo-controlled double-blind study (ZOledroNate treatment in Efficacy to osteoporosis; ZONE study).

Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA·2016

Comparing immunocompetent and immunodeficient mice as animal models for bone tissue engineering.

Oral diseases·2015

Panoramic radiography measurements, osteoporosis diagnoses and fractures in Japanese men and women.

Oral diseases·2014

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

Results from the VANISH study: A prospective multicenter study validating a single-nucleotide polymorphism-based noninvasive prenatal test to assess aneuploidy risk in surviving twins of vanishing twin pregnancies.

Pregnancy (Hoboken, N.J.)·2026

Interobserver reliability and digital morphometric characterization of constitutional chromosomal heteromorphisms in clinical cytogenetics.

Human genetics·2026

Related Experiment Videos

A cytogenetic survey of consecutive liveborn infants-incidence and type of chromosome abnormalities

Related Concept Videos

Long waiting time before tooth extraction may increase delayed wound healing in elderly Japanese.

Issues with the surgical treatment of antiresorptive agent-related osteonecrosis of the jaws.

Significant improvement of bone mineral density and bone turnover markers by denosumab therapy in bisphosphonate-unresponsive patients.

Efficacy and safety of once-yearly zoledronic acid in Japanese patients with primary osteoporosis: two-year results from a randomized placebo-controlled double-blind study (ZOledroNate treatment in Efficacy to osteoporosis; ZONE study).

Comparing immunocompetent and immunodeficient mice as animal models for bone tissue engineering.

Panoramic radiography measurements, osteoporosis diagnoses and fractures in Japanese men and women.

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.

FAT1 generates a nuclear fragment that impairs DNA damage repair in gastric cancer.

Results from the VANISH study: A prospective multicenter study validating a single-nucleotide polymorphism-based noninvasive prenatal test to assess aneuploidy risk in surviving twins of vanishing twin pregnancies.

Loss-of-function variants in CFAP57, SEPTIN4, SPEM2, and CFAP46 cause asthenoteratozoospermia.

Chromosome-Scale Assembly of Novel Caenorhabditis sp. 65 (strain JU4118).

Comparative analysis of chromosome interaction networks in 12 human cell types using Hi-C.

Interobserver reliability and digital morphometric characterization of constitutional chromosomal heteromorphisms in clinical cytogenetics.

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A cytogenetic survey of consecutive liveborn infants-incidence and type of chromosome abnormalities

Related Concept Videos

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