Genetic screening of Congenital Short Bowel Syndrome patients confirms CLMP as the major gene involved in the recessive form of this disorder

Maria Alves; Danny Halim; R Maroofian; Bianca de Graaf; R Rooman; CS Van Der Werf; E van de Vijver; M Y V Mehrjardi; M Aflatoonian; B A Chioza; E L Baple; M Dehghani; A H Crosby; Robert Hofstra

doi:10.1038/ejhg.2016.58

Genetic screening of Congenital Short Bowel Syndrome patients confirms CLMP as the major gene involved in the recessive form of this disorder

Maria Alves, Danny Halim, R Maroofian, Bianca de Graaf, R Rooman, CS Van Der Werf, E van de Vijver, M Y V Mehrjardi, M Aflatoonian, B A Chioza, E L Baple, M Dehghani, A H Crosby, Robert Hofstra

Clinical Genetics

Research output: Contribution to journal › Article › Academic › peer-review

17 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	1627-1629
Number of pages	3
Journal	European Journal of Human Genetics
Volume	24
Issue number	11
DOIs	https://doi.org/10.1038/ejhg.2016.58
Publication status	Published - 2016

Research programs

EMC MGC-02-96-01

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10.1038/ejhg.2016.58

Cite this

Alves, M., Halim, D., Maroofian, R., de Graaf, B., Rooman, R., Van Der Werf, CS., van de Vijver, E., Mehrjardi, M. Y. V., Aflatoonian, M., Chioza, B. A., Baple, E. L., Dehghani, M., Crosby, A. H., & Hofstra, R. (2016). Genetic screening of Congenital Short Bowel Syndrome patients confirms CLMP as the major gene involved in the recessive form of this disorder. European Journal of Human Genetics, 24(11), 1627-1629. https://doi.org/10.1038/ejhg.2016.58

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author = "Maria Alves and Danny Halim and R Maroofian and {de Graaf}, Bianca and R Rooman and {Van Der Werf}, CS and {van de Vijver}, E and Mehrjardi, {M Y V} and M Aflatoonian and Chioza, {B A} and Baple, {E L} and M Dehghani and Crosby, {A H} and Robert Hofstra",

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Alves, M, Halim, D, Maroofian, R, de Graaf, B, Rooman, R, Van Der Werf, CS, van de Vijver, E, Mehrjardi, MYV, Aflatoonian, M, Chioza, BA, Baple, EL, Dehghani, M, Crosby, AH & Hofstra, R 2016, 'Genetic screening of Congenital Short Bowel Syndrome patients confirms CLMP as the major gene involved in the recessive form of this disorder', European Journal of Human Genetics, vol. 24, no. 11, pp. 1627-1629. https://doi.org/10.1038/ejhg.2016.58

TY - JOUR

T1 - Genetic screening of Congenital Short Bowel Syndrome patients confirms CLMP as the major gene involved in the recessive form of this disorder

AU - Alves, Maria

AU - Halim, Danny

AU - Maroofian, R

AU - de Graaf, Bianca

AU - Rooman, R

AU - Van Der Werf, CS

AU - van de Vijver, E

AU - Mehrjardi, M Y V

AU - Aflatoonian, M

AU - Chioza, B A

AU - Baple, E L

AU - Dehghani, M

AU - Crosby, A H

AU - Hofstra, Robert

PY - 2016

Y1 - 2016

U2 - 10.1038/ejhg.2016.58

DO - 10.1038/ejhg.2016.58

M3 - Article

C2 - 27352967

SN - 1018-4813

VL - 24

SP - 1627

EP - 1629

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 11

ER -