部分C型トリソミーの皮膚文字

M A Crawfurd

Lancet (London, England)

|June 1, 1968

まとめ

No abstract available in PubMed .

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関連する実験動画

部分C型トリソミーの皮膚文字

関連する概念動画

Anderson-Fabry disease.

Alport's syndrome.

Anderson-Fabry disease--family linkage studies using two polymorphic X-linked DNA probes.

Recognising placental steroid sulphatase deficiency.

Review: genetics of steroid sulphatase deficiency and X-linked ichthyosis.

Congenital haemolytic anaemia resulting from glucose phosphate isomerase deficiency: genetics, clinical picture, and prenatal diagnosis.

Inherited retinal degenerations: clinical phenotypes and emerging therapies.

Documenting hospice care.

After the wood chipper.

Assisted dying and the silencing of medicine's next generation.

Linguistic pragmatism: a woman with progressive abdominal pain in Thailand.

Medical compartmentalisation: a patient with chromosome 22q11.2 deletion syndrome in Japan.

関連する実験動画

部分C型トリソミーの皮膚文字

関連する概念動画

Anderson-Fabry disease.

Alport's syndrome.

Anderson-Fabry disease--family linkage studies using two polymorphic X-linked DNA probes.

Recognising placental steroid sulphatase deficiency.

Review: genetics of steroid sulphatase deficiency and X-linked ichthyosis.

Congenital haemolytic anaemia resulting from glucose phosphate isomerase deficiency: genetics, clinical picture, and prenatal diagnosis.

Inherited retinal degenerations: clinical phenotypes and emerging therapies.

Documenting hospice care.

After the wood chipper.

Assisted dying and the silencing of medicine's next generation.

Linguistic pragmatism: a woman with progressive abdominal pain in Thailand.

Medical compartmentalisation: a patient with chromosome 22q11.2 deletion syndrome in Japan.

関連する実験動画

部分C型トリソミーの皮膚文字

関連する概念動画

関連記事

Anderson-Fabry disease.

Alport's syndrome.

Anderson-Fabry disease--family linkage studies using two polymorphic X-linked DNA probes.

Recognising placental steroid sulphatase deficiency.

Review: genetics of steroid sulphatase deficiency and X-linked ichthyosis.

Congenital haemolytic anaemia resulting from glucose phosphate isomerase deficiency: genetics, clinical picture, and prenatal diagnosis.

Inherited retinal degenerations: clinical phenotypes and emerging therapies.

Documenting hospice care.

After the wood chipper.

Assisted dying and the silencing of medicine's next generation.

Linguistic pragmatism: a woman with progressive abdominal pain in Thailand.

Medical compartmentalisation: a patient with chromosome 22q11.2 deletion syndrome in Japan.

関連する実験動画

部分C型トリソミーの皮膚文字

関連する概念動画

関連記事

Anderson-Fabry disease.

Alport's syndrome.

Anderson-Fabry disease--family linkage studies using two polymorphic X-linked DNA probes.

Recognising placental steroid sulphatase deficiency.

Review: genetics of steroid sulphatase deficiency and X-linked ichthyosis.

Congenital haemolytic anaemia resulting from glucose phosphate isomerase deficiency: genetics, clinical picture, and prenatal diagnosis.

Inherited retinal degenerations: clinical phenotypes and emerging therapies.

Documenting hospice care.

After the wood chipper.

Assisted dying and the silencing of medicine's next generation.

Linguistic pragmatism: a woman with progressive abdominal pain in Thailand.

Medical compartmentalisation: a patient with chromosome 22q11.2 deletion syndrome in Japan.