Pallister W Syndrome
What's New
Last Posted: Sep 06, 2016
- [Prenatal diagnosis of a Pallister-Killian syndrome case through analysis of a supernumerary chromosome using single nucleotide polymorphism array].
Li Suping, et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2016 10 (5) 682-5 - [Prenatal diagnosis of a case of Pallister-Killian syndrome].
Xi Hui, et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2015 2 (1) 73-6 - Pallister W syndrome
From NCATS Genetic and Rare Diseases Information Center - Pallister-Hall syndrome
From NCATS Genetic and Rare Diseases Information Center - Identification of somatic chromosomal abnormalities in hypothalamic hamartoma tissue at the GLI3 locus.
Craig David W, et al. American journal of human genetics 2008 2 (2) 366-74
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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- Page last reviewed:Feb 1, 2024
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