Clinical, cytogenetic, and molecular observations in a patient with Pallister-Killian-syndrome with an unusual karyotype-Reference-Cited by-同舟云学术

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Clinical, cytogenetic, and molecular observations in a patient with Pallister-Killian-syndrome with an unusual karyotype

Published:2003-11-03 Issue:3 Volume:123A Page:296-300
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Leube Barbara,Majewski Frank,Gebauer J�rgen,Royer-Pokora Brigitte

Publisher

Wiley

Subject

Genetics (clinical)

Reference20 articles.

1. Cytogenetic and molecular analysis in trisomy 12p

2. Prezygotic origin of the isochromosome 12p in Pallister-Killian syndrome

3. Isochromosomes 12p and 9p: parental origin and possible mechanisms of formation

4. Trisomy 12p Syndrome: A Chromosomal Disorder Associated with Generalized 3-Hz Spike and Wave Discharges

Cited by 19 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Structural brain abnormalities in Pallister-Killian syndrome: a neuroimaging study of 31 children;Orphanet Journal of Rare Diseases;2024-03-08

2. Neuroimaging findings in Pallister-Killian syndrome;The Neuroradiology Journal;2017-12-20

3. Pallister–Killian syndrome: Cytogenetics and molecular investigations of mosaic tetrasomy 12p in prenatal chorionic villus and in amniocytes. Strategy of prenatal diagnosis;Taiwanese Journal of Obstetrics and Gynecology;2016-12

4. Cytogenomic delineation and clinical follow-up of 10 Brazilian patients with Pallister-Killian syndrome;Molecular Cytogenetics;2015-06-26

5. Pallister-Killian syndrome: a study of 22 British patients;Journal of Medical Genetics;2015-04-17

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