Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders

M. S. Oud; B. J. Houston; Lummila Volozonoka; F. K. Mastrorosa; B. Alobaidi; P.F. de Vries; G. Astuti; L. Ramos; R. Burke; R. I. McLachlan; M. K. O'Bryan; J. A. Veltman; H. E. Chemes; H. Sheth

Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders

M. S. Oud, B. J. Houston, Lummila Volozonoka, F. K. Mastrorosa, B. Alobaidi, P.F. de Vries, G. Astuti, L. Ramos, R. Burke, R. I. McLachlan, M. K. O'Bryan, J. A. Veltman, H. E. Chemes, H. Sheth

Rīga Stradiņš University

Research output: Contribution to journal › Meeting Abstract › peer-review

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Original language	English
Pages (from-to)	29-30
Journal	European Journal of Human Genetics
Volume	28
Issue number	SUPPL 1
Publication status	Published - Dec 2020
Event	53rd European Society of Human Genetics (ESHG) Conference - Virtual Conference Duration: 6 Jun 2020 → 9 Jun 2020 Conference number: 53 https://www.nature.com/collections/eaabehjbcc/

Field of Science*

1.6 Biological sciences

Publication Type*

3.3. Publications in conference proceedings indexed in Web of Science and/or Scopus database

Access to Document

Exome sequencing reveals variants in known and novelFinal published version, 3.97 MB

https://www.nature.com/articles/s41431-020-00740-6.pdf

Cite this

Oud, M. S., Houston, B. J., Volozonoka, L., Mastrorosa, F. K., Alobaidi, B., de Vries, P. F., Astuti, G., Ramos, L., Burke, R., McLachlan, R. I., O'Bryan, M. K., Veltman, J. A., Chemes, H. E., & Sheth, H. (2020). Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders. European Journal of Human Genetics, 28(SUPPL 1), 29-30. https://www.nature.com/articles/s41431-020-00740-6.pdf

@article{5377b5e341df4d5b8083953b2d760ed6,

title = "Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders",

author = "Oud, {M. S.} and Houston, {B. J.} and Lummila Volozonoka and Mastrorosa, {F. K.} and B. Alobaidi and {de Vries}, P.F. and G. Astuti and L. Ramos and R. Burke and McLachlan, {R. I.} and O'Bryan, {M. K.} and Veltman, {J. A.} and Chemes, {H. E.} and H. Sheth",

year = "2020",

month = dec,

language = "English",

volume = "28",

pages = "29--30",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

publisher = "Springer Nature",

number = "SUPPL 1",

note = "53rd European Society of Human Genetics (ESHG) Conference, ESHG ; Conference date: 06-06-2020 Through 09-06-2020",

url = "https://www.nature.com/collections/eaabehjbcc/",

}

Oud, MS, Houston, BJ, Volozonoka, L, Mastrorosa, FK, Alobaidi, B, de Vries, PF, Astuti, G, Ramos, L, Burke, R, McLachlan, RI, O'Bryan, MK, Veltman, JA, Chemes, HE & Sheth, H 2020, 'Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders', European Journal of Human Genetics, vol. 28, no. SUPPL 1, pp. 29-30. <https://www.nature.com/articles/s41431-020-00740-6.pdf>

TY - JOUR

T1 - Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders

AU - Oud, M. S.

AU - Houston, B. J.

AU - Volozonoka, Lummila

AU - Mastrorosa, F. K.

AU - Alobaidi, B.

AU - de Vries, P.F.

AU - Astuti, G.

AU - Ramos, L.

AU - Burke, R.

AU - McLachlan, R. I.

AU - O'Bryan, M. K.

AU - Veltman, J. A.

AU - Chemes, H. E.

AU - Sheth, H.

N1 - Conference code: 53

PY - 2020/12

Y1 - 2020/12

M3 - Meeting Abstract

SN - 1018-4813

VL - 28

SP - 29

EP - 30

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - SUPPL 1

T2 - 53rd European Society of Human Genetics (ESHG) Conference

Y2 - 6 June 2020 through 9 June 2020

ER -