(Q56929847)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10706364%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

title

Holoprosencephaly, hypertelorism, and ectrodactyly in a boy with an apparently balanced de novo t(2;4) (q14.2;q35) (English)

1 reference

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4 November 2019

1 reference

1 reference

Lucina Bobadilla-Morales

3

1 reference

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4 November 2019

Lucina Bobadilla-Morales

4

1 reference

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4 November 2019

author name string

A Corona-Rivera

1

1 reference

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4 November 2019

J R Corona-Rivera

2

1 reference

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4 November 2019

T A García-Cobian

5

1 reference

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4 November 2019

E Corona-Rivera

6

1 reference

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4 November 2019

publication date

1 February 2000

1 reference

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American Journal of Medical Genetics Part A

4 November 2019

published in

1 reference

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4 November 2019

volume

90

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4 November 2019

issue

5

1 reference

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4 November 2019

page(s)

423-426

1 reference

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Perspectives on holoprosencephaly: Part I. Epidemiology, genetics, and syndromology

4 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2820000228%2990%3A5%3C423%3A%3AAID-AJMG12%3E3.0.CO%3B2-K

Perspectives on holoprosencephaly: Part III. Spectra, distinctions, continuities, and discontinuities

21 January 2018

1 reference

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Novel translocation (2;4) with consistent involvement of 2p23 in acute nonlymphocytic leukemia (M2)

21 January 2018

1 reference

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Private multiple congenital anomaly syndromes may result from unbalanced subtle translocations: t(2q;4p) explains the Lambotte syndrome

21 January 2018

1 reference

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Association of holoprosencephaly, ectrodactyly, cleft lip/cleft palate and hypertelorism: a possible third case

21 January 2018

1 reference

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Chromosome studies in in-vitro fertilization patients.

21 January 2018

1 reference

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Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephaly

21 January 2018

1 reference

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Translocation (2;4)(p23;q25): an additional case of a new recurrent anomaly in acute myeloid leukemia

21 January 2018

1 reference

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Tyrosinase positive albinism with familial 46,XY,t(2;4) (q31.2;q31.22) balanced translocation

21 January 2018

1 reference

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10.1002/(SICI)1096-8628(20000228)90:5<423::AID-AJMG12>3.0.CO;2-K

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10706364%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

1 reference