An inherited pericentric chromosomal inversion (46, inv3 [p-q+]) associated with skeletal anomalies

Author:

Cohen Maimon M.,Davidson Ronald G.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference19 articles.

1. Chromosome studies in 5 cases of coloboma of the iris;Lele;Lancet,1965

2. Chromosome anomalies;Carr;Trans. Amer. Ass. Genitourin. Surg.,1962

3. Inversion pericentrique probable du chromosome no. 2 et malformations congenitales chez un garcon;Grouchy;Ann. Genet.,1963

4. Syndrome de Turner et inversion pericentrique du chromosome no. 2 [45,X,2(p+q-)];Hooft;Ann. Genet.,1968

5. Inherited pericentric inversion of chromosome number two: A linkage study;Weitkamp;Ann. Hum. Genet.,1969

Cited by 5 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. Oculofacial Manifestations of Chromosomal Aberrations;The Eye in Pediatric Systemic Disease;2017

2. A RETARDED CHILD WITH A 46XX,3p-q+ CHROMOSOME KARYOTYPE;Journal of Intellectual Disability Research;2008-06-28

3. Apparent Coats' Disease and Pericentric Inversion of Chromosome 3;American Journal of Ophthalmology;1987-07

4. A fetus with recombinant of chromosome 8 inherited from her carrier father;Human Genetics;1978

5. Chromosomal variants with normal phenotype in Man;Journal of Human Evolution;1973-07

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