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1
Holoprosencephaly and cytogenetic findings: further information.
Am J Med Genet. 1989 Oct;34(2):265. doi: 10.1002/ajmg.1320340229.
3
Holoprosencephaly and interstitial deletion of 2(p2101p2109).
Am J Med Genet. 1989 Oct;34(2):252-4. doi: 10.1002/ajmg.1320340226.
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Prenatal detection of cyclopia associated with interstitial deletion of 2p.
Am J Med Genet. 1989 Oct;34(2):268-70. doi: 10.1002/ajmg.1320340231.
7
Trisomy for the distal part of the short arm of chromosome 3.
Helv Paediatr Acta. 1986 Mar;41(6):509-13.
8
Prenatal diagnosis of partial monosomy 3p and partial trisomy 2p in a fetus associated with shortening of the long bones and a single umbilical artery.
Prenat Diagn. 1996 Mar;16(3):270-5. doi: 10.1002/(SICI)1097-0223(199603)16:3<270::AID-PD836>3.0.CO;2-0.
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Prenatal detection of de novo inversion of chromosome (2) (p13q11.2) and postnatal follow-up.
Prenat Diagn. 1996 Apr;16(4):366-70. doi: 10.1002/(SICI)1097-0223(199604)16:4<366::AID-PD863>3.0.CO;2-Z.

引用本文的文献

1
Holoprosencephaly-polydactyly/pseudotrisomy 13: a presentation of two new cases and a review of the literature.
Clin Dysmorphol. 2012 Oct;21(4):183-190. doi: 10.1097/MCD.0b013e3283551fd0.

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