(Q48887067)

16 February 2018

title

Holoprosencephaly associated with an apparent isolated 2q37.1-->2q37.3 deletion. (English)

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16 February 2018

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1

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author name string

Zaleski DH

series ordinal

2

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16 February 2018

Sanger WG

series ordinal

3

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16 February 2018

Adickes ED

series ordinal

4

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16 February 2018

publication date

1 May 2001

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16 February 2018

American Journal of Medical Genetics Part A

published in

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16 February 2018

volume

100

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issue

3

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16 February 2018

page(s)

179-181

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Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired

cites work

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

21 January 2018

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Holoprosencephaly: epidemiologic and clinical characteristics of a California population

21 January 2018

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Deletion of chromosome 2q37 and autism: a distinct subtype?

21 January 2018

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Holoprosencephaly: a defect in brain patterning.

21 January 2018

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Growth factor properties of VIP during early brain development. Whole embryo culture and in vivo studies

21 January 2018

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Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination

21 January 2018

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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

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Palpebral fissure size in newborn infants

21 January 2018

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Holoprosencephaly and related midline cerebral anomalies: a review

21 January 2018

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Chromosomal mapping of A1 and A2 adenosine receptors, VIP receptor, and a new subtype of serotonin receptor

21 January 2018

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The HOX complex neighbored by the EVX gene, as well as two other homeobox-containing genes, the GBX-class and the EN-class, are located on the same chromosomes 2 and 7 in humans

21 January 2018

1 reference

Microdeletion of chromosome sub-band 2q37.3 in two patients with abnormal situs viscerum

21 January 2018

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Mutations in the human Sonic Hedgehog gene cause holoprosencephaly

21 January 2018

1 reference

Structure and chromosomal localization of the human PD-1 gene (PDCD1)

21 January 2018

1 reference

Lambotte syndrome: microcephaly, holoprosencephaly, intrauterine growth retardation, facial anomalies, and early lethality--a new sublethal multiple congenital anomaly/mental retardation syndrome in four sibs

21 January 2018

1 reference

Molecular mechanisms of holoprosencephaly

21 January 2018

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Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly

21 January 2018

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Holoprosencephaly in the west of Scotland 1975-1994.

21 January 2018

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Localization of the gene for high-density lipoprotein binding protein (HDLBP) to human chromosome 2q37

21 January 2018

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Holoprosencephaly in infants of diabetic mothers

21 January 2018

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Prenatal diagnosis of terminal deletion 7q and partial trisomy 3p in fetuses with holoprosencephaly

21 January 2018

1 reference

Alobar Holoprosencephaly (Arhinencephaly) with Median Cleft Lip and Palate: Clinical, Electroencephalographic and Nosologic Considerations (Part 1 of 2)

21 January 2018

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Holoprosencephaly in RSH/Smith-Lemli-Opitz syndrome: does abnormal cholesterol metabolism affect the function of Sonic Hedgehog?

21 January 2018

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Arhinencephaly. The spectrum of associated malformations

21 January 2018

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The dup(3)(p25 leads to pter) syndrome: a case with holoprosencephaly

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/AJMG.1245

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16 February 2018

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16 February 2018