Monozygotic twins concordant for Prader-Willi syndrome

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

Preputial cyst in the newborn: a case report.

The Pan African medical journal·2026

Use of whole blood in pediatric congenital heart surgery.

JTCVS open·2026

Managing cyanotic neonates with tetralogy of Fallot: A national perspective on surgical approaches.

JTCVS open·2026

Assessing the applicability of Society of Thoracic Surgeons-European Association for Cardio-Thoracic Surgery (STAT) categories in neonatal and low-weight congenital cardiac surgery: Insights from 20 years at a single center.

JTCVS open·2026

Dyke-Davidoff-Masson Syndrome Underlying Hemiplegic Cerebral Palsy in an Adolescent: A Case Report.

Cureus·2026

Streamlining Urinary Tract Infection Evaluation in a Large Pediatric Hospital System: Feasibility of Reflex Urine Culture After Urinalysis With Microscopy.

Archives of pathology & laboratory medicine·2026

Related Experiment Videos

Monozygotic twins concordant for Prader-Willi syndrome

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.

Preputial cyst in the newborn: a case report.

Use of whole blood in pediatric congenital heart surgery.

Managing cyanotic neonates with tetralogy of Fallot: A national perspective on surgical approaches.

Assessing the applicability of Society of Thoracic Surgeons-European Association for Cardio-Thoracic Surgery (STAT) categories in neonatal and low-weight congenital cardiac surgery: Insights from 20 years at a single center.

Dyke-Davidoff-Masson Syndrome Underlying Hemiplegic Cerebral Palsy in an Adolescent: A Case Report.

Streamlining Urinary Tract Infection Evaluation in a Large Pediatric Hospital System: Feasibility of Reflex Urine Culture After Urinalysis With Microscopy.

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Monozygotic twins concordant for Prader-Willi syndrome

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