(Q33653139)

28 July 2017

1 reference

title

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

1 reference

28 July 2017

Reddy KS

1

1 reference

28 July 2017

Flannery D

series ordinal

2

1 reference

28 July 2017

Farrer RJ

series ordinal

3

1 reference

28 July 2017

publication date

1 June 1999

1 reference

American Journal of Medical Genetics Part A

28 July 2017

published in

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28 July 2017

volume

84

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28 July 2017

issue

5

1 reference

28 July 2017

page(s)

460-468

1 reference

A submicroscopic deletion in Xq26 associated with familial situs ambiguus

28 July 2017

cites work

1 reference

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The human PD-1 gene: complete cDNA, genomic organization, and developmentally regulated expression in B cell progenitors

21 January 2018

1 reference

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Small terminal deletions of the long arm of chromosome 2: two new cases.

21 January 2018

1 reference

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Albright's hereditary osteodystrophy: a review

21 January 2018

1 reference

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Asplenia syndrome in a child with a balanced reciprocal translocation of chromosomes 11 and 20 [46,XX,t(11;20)(q13.1;q13.13)].

21 January 2018

1 reference

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Oxford medical databases.

21 January 2018

1 reference

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Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37).

21 January 2018

1 reference

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Fish mapping of a translocation breakpoint at 6q21 (or q22) in a patient with heterotaxia.

21 January 2018

1 reference

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Smallest terminal deletion of the long arm of chromosome 2 in a mildly affected boy

21 January 2018

1 reference

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Routine use of methods for improved G-band resolution in a population of patients with malformations and developmental delay

21 January 2018

1 reference

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Discovery of three novel G-protein-coupled receptor genes

21 January 2018

1 reference

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Paternal isodisomy of chromosome 7 associated with complete situs inversus and immotile cilia

21 January 2018

1 reference

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Albright hereditary osteodystrophy and del(2)(q37.3) in four unrelated individuals

21 January 2018

1 reference

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RDCI, the vasoactive intestinal peptide receptor: a candidate gene for the features of Albright hereditary osteodystrophy associated with deletion of 2q37

21 January 2018

1 reference

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The pattern of shortening of the bones of the hand in PHP and PPHP--A comparison with brachydactyly E, Turner Syndrome, and acrodysostosis

21 January 2018

1 reference

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

21 January 2018

1 reference

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21 January 2018

1 reference

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Wilms' tumor and gonadal dysgenesis in a child with the 2q37.1 deletion syndrome

21 January 2018

1 reference

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Terminal deletion of the long arm of chromosome 2 in a premature infant with karyotype: 46,XY,del(2)(q37).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990611%2984%3A5%3C460%3A%3AAID-AJMG10%3E3.0.CO%3B2-L

Autopsy findings in a severely affected infant with a 2q terminal deletion

21 January 2018

1 reference

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Balanced translocation 12/13 and situs abnormalities: homology of early pattern formation in man and lower organisms?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990611%2984%3A5%3C460%3A%3AAID-AJMG10%3E3.0.CO%3B2-L

10.1002/(SICI)1096-8628(19990611)84:5<460::AID-AJMG10>3.0.CO;2-L

21 January 2018

Identifiers

DOI

1 reference

28 July 2017

1 reference