A rare chromosomal abnormality inherited from the mother in a boy conceived after intracytoplasmic sperm injection: a case report

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A rare chromosomal abnormality inherited from the mother in a boy conceived after intracytoplasmic sperm injection: a case report

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2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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2012年学术文章

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A rare chromosomal abnormality ...... sperm injection: a case report

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A rare chromosomal abnormality ...... sperm injection: a case report

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A rare chromosomal abnormality ...... sperm injection: a case report

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A rare chromosomal abnormality ...... sperm injection: a case report

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A rare chromosomal abnormality ...... sperm injection: a case report

@ast

A rare chromosomal abnormality ...... sperm injection: a case report

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P1476

A rare chromosomal abnormality ...... sperm injection: a case report

@en

P2093

Ding Ma

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Gui-jin Zhu

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Han-wang Zhang

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Hong Tian

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Li Yin

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Long-jie Gu

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P2860

Structural organization of the human short-chain acyl-CoA dehydrogenase gene

Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish origin

Three cases of partial trisomy 7q owing to rare structural rearrangements of chromosome 7.

FISH preimplantation diagnosis of chromosome aneuploidy in recurrent pregnancy wastage.

Improvements in cytogenetic slide preparation: controlled chromosome spreading, chemical aging and gradual denaturing.

Chromosome abnormalities in human beings.

Tandem duplication of the terminal band of the long arm of chromosome 7 (dir dup (7)(q36----qter)).

Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia.

Strong variable clinical presentation in 3 patients with 7q terminal deletion.

A fourteen years follow-up of a case of partial trisomy 12q and monosomy 12p recombinants of a familial pericentric inversion of chromosome 12: clinical, cytogenetic and molecular observations.

P2888

s10815-012-9796-9

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917-920

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P31

scholarly article

case report

P356

10.1007/S10815-012-9796-9

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P433

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P478

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P577

2012-05-24T00:00:00Z

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22622526

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P932

3463672

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