(Q28943387)

19

0 references

Anita Rauch

34

0 references

Diana Zelenika

6

0 references

Chrysovalanto Mamasoula

3

Chrysovalanto Mamasoula

1 reference

14 March 2017

16

Darroch Hall

1 reference

14 March 2017

28

David Winlaw

1 reference

14 March 2017

Shoumo Bhattacharya

27

0 references

Alex V Postma

Alex V. Postma

4

0 references

Marc Gewillig

Marc Gewillig

30

0 references

Mark Lathrop

35

Javier T Granados-Riveron

G. Mark Lathrop

1 reference

14 March 2017

25

A. Graham Stuart

1 reference

14 March 2017

36

Bernard D. Keavney

1 reference

14 March 2017

37

Judith A. Goodship

1 reference

14 March 2017

1

Heather J. Cordell

1 reference

14 March 2017

10

Javier Granados Riveron

1 reference

14 March 2017

5

Jamie Bentham

1 reference

14 March 2017

9

Catherine Cosgrove

1 reference

14 March 2017

31

Jeroen Breckpot

1 reference

14 March 2017

21

Kerry Setchfield

1 reference

14 March 2017

23

Chris Thornborough

1 reference

14 March 2017

12

Rachel Soemedi

1 reference

14 March 2017

15

Thahira J. Rahman

1 reference

14 March 2017

8

Gillian Blue

1 reference

14 March 2017

2

Ana Töpf

1 reference

14 March 2017

7

Simon Heath

1 reference

14 March 2017

18

Aelko H. Zwinderman

1 reference

14 March 2017

29

Seema Mital

1 reference

14 March 2017

33

Antoon F. M. Moorman

1 reference

14 March 2017

17

Barbara J. M. Mulder

1 reference

14 March 2017

Rebecca Darlay

11

1 reference

14 March 2017

Ian J. Wilson

13

1 reference

14 March 2017

Kristin L. Ayers

14

1 reference

14 March 2017

J. David Brook

20

1 reference

14 March 2017

Frances A. Bu'Lock

22

1 reference

14 March 2017

John O'Sullivan

24

1 reference

14 March 2017

Jonathan Parsons

describes a project that uses

26

1 reference

14 March 2017

1 April 2013

1 reference

14 March 2017

Human Molecular Genetics

1 reference

14 March 2017

22

1 reference

14 March 2017

1473–1481

1 reference

14 March 2017

7

1 reference

14 March 2017

genome-wide association study

1 reference

based on heuristic

inferred from title

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16 March 2017

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16 March 2017

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16 March 2017

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16 March 2017

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Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

16 March 2017

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Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome

16 March 2017

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Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis

16 March 2017

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Endothelial neuropilin disruption in mice causes DiGeorge syndrome-like malformations via mechanisms distinct to those caused by loss of Tbx1

3 June 2018

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Inheritance of coronary artery disease in men: an analysis of the role of the Y chromosome

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A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium

3 June 2018

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De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot

3 June 2018

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Mutations in the heparan-sulfate proteoglycan glypican 6 (GPC6) impair endochondral ossification and cause recessive omodysplasia

3 June 2018

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3 June 2018

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Racial and temporal variations in the prevalence of heart defects

3 June 2018

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3 June 2018

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Preliminary definition of a "critical region" of chromosome 13 in q32: report of 14 cases with 13q deletions and review of the literature.

3 June 2018

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A case report of a patient with retinoblastoma and chromosome 13q deletion: assignment of a new gene (gene for LCP1) on human chromosome 13.

3 June 2018

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GPC5 rs2352028 variant and risk of lung cancer in never smokers

3 June 2018

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22q11.2 Deletion Syndrome is under-recognised in adult patients with tetralogy of Fallot and pulmonary atresia.

21 January 2018

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21 January 2018

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Recurrence of Congenital Heart Defects in Families

26 November 2018

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12 December 2020

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