Newborn with Supernumerary Marker Chromosome Derived from Chromosomes 11 And 22- A Case Report.

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Newborn with Supernumerary Marker Chromosome Derived from Chromosomes 11 And 22- A Case Report.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年學術文章

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2016年學術文章

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2016年學術文章

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Newborn with Supernumerary Mar ...... omes 11 And 22- A Case Report.

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Newborn with Supernumerary Mar ...... omes 11 And 22- A Case Report.

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Newborn with Supernumerary Mar ...... omes 11 And 22- A Case Report.

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P1476

Newborn with Supernumerary Mar ...... omes 11 And 22- A Case Report.

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Mahmoud Nori-Shadkam

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Masoud Dehghan Tezerjani

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Mohammad Yahya Vahidi Mehrjardi

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Mohammadreza Dehghani

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Seyed Mehdi Kalantar

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Magic roundabout is a new member of the roundabout receptor family that is endothelial specific and expressed at sites of active angiogenesis

Partial trisomy 2q33.3-q37.3 in a patient with an inverted duplicated neocentric marker chromosome.

Cryptic duplication of the distal segment of 22q due to a translocation (21;22): three case reports and a review of the literature.

Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity?

Characterisation of supernumerary chromosomal markers: a study of 13 cases.

A molecular and FISH approach to determining karyotype and phenotype correlations in six patients with supernumerary marker(22) chromosomes.

Severe psychomotor delay in a severe presentation of cat-eye syndrome.

Upper airway malformation associated with partial trisomy 11q.

Forty four probands with an additional "marker" chromosome.

P304

376-380

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P31

scholarly article

case report

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P478

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P577

2016-03-01T00:00:00Z

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27141501

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P932

4851753

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