Cytogenetic survey of primary amenorrhea

QTL analysis of body weight and carcass body length traits in an F2 intercross between Landrace and Korean native pigs.

Animal genetics·2014

QTL analysis of white blood cell, platelet and red blood cell-related traits in an F2 intercross between Landrace and Korean native pigs.

Animal genetics·2011

Novel alternative splicing by exon skipping in KIT associated with whole-body roan in an intercrossed population of Landrace and Korean Native pigs.

Animal genetics·2011

Nanocrystallization of the Fd3m Ti2Ni-type phase in Hf-based metallic glasses.

Journal of nanoscience and nanotechnology·2003

Embryogenomics: developmental biology meets genomics.

Trends in biotechnology·2001

Random monoallelic expression of three genes clustered within 60 kb of mouse t complex genomic DNA.

Genome research·2001

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

A Rare Finding of Mosaic 45,XX,der(13;21)(q10;q10)[15]/46,XX,r(13)(p11.2q33) Following Abnormal Prenatal Chromosomal Microarray Testing.

Case reports in genetics·2026

Corrigendum to "Determination of human papillomavirus prevalence in the female population from Zanjan, Iran" [Prev. Med. Rep. 62 (2026) 103406].

Preventive medicine reports·2026

A Rare Mimicker: Renal Endometriosis and Its Diagnostic Pitfalls-Review of Reported Cases.

Diagnostics (Basel, Switzerland)·2026

Thyroid-stimulating hormone-secreting pituitary neuroendocrine tumor (TSH-PitNet) diagnosed during pregnancy and treated with a somatostatin analog.

Taiwanese journal of obstetrics & gynecology·2026

Intramyometrial mature cystic teratoma in a Rudimentary horn in Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome: A Rare Surgical Finding.

Journal of pediatric and adolescent gynecology·2026

Persistent progesterone elevation in infertility revealing non-classic P450 oxidoreductase deficiency: 2 cases.

JCEM case reports·2026

Related Experiment Videos

Cytogenetic survey of primary amenorrhea

Related Concept Videos

QTL analysis of body weight and carcass body length traits in an F2 intercross between Landrace and Korean native pigs.

QTL analysis of white blood cell, platelet and red blood cell-related traits in an F2 intercross between Landrace and Korean native pigs.

Novel alternative splicing by exon skipping in KIT associated with whole-body roan in an intercrossed population of Landrace and Korean Native pigs.

Nanocrystallization of the Fd3m Ti2Ni-type phase in Hf-based metallic glasses.

Embryogenomics: developmental biology meets genomics.

Random monoallelic expression of three genes clustered within 60 kb of mouse t complex genomic DNA.

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.

A Rare Finding of Mosaic 45,XX,der(13;21)(q10;q10)[15]/46,XX,r(13)(p11.2q33) Following Abnormal Prenatal Chromosomal Microarray Testing.

Corrigendum to "Determination of human papillomavirus prevalence in the female population from Zanjan, Iran" [Prev. Med. Rep. 62 (2026) 103406].

A Rare Mimicker: Renal Endometriosis and Its Diagnostic Pitfalls-Review of Reported Cases.

Thyroid-stimulating hormone-secreting pituitary neuroendocrine tumor (TSH-PitNet) diagnosed during pregnancy and treated with a somatostatin analog.

Intramyometrial mature cystic teratoma in a Rudimentary horn in Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome: A Rare Surgical Finding.

Persistent progesterone elevation in infertility revealing non-classic P450 oxidoreductase deficiency: 2 cases.

Related Experiment Videos

Cytogenetic survey of primary amenorrhea

Related Concept Videos

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