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Hoefsloot, Lies H
227
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Online (227)
Mediatypes
Articles (Online) (140)
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english (220)
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1
Response to the comment on Diderich et al. "The role of a m..:
Diderich, Karin E.M.
;
Klapwijk, Jasmijn E.
;
van der Schoot, Vyne
...
European Journal of Medical Genetics. 67 (2024) - p. 104884 , 2024
Link:
https://doi.org/10.1016/..
?
2
Identification of Rare Variants Involved in High Myopia Unr..:
Haarman, Annechien E.G.
;
Klaver, Caroline C.W.
;
Tedja, Milly S.
...
Ophthalmology Science. 3 (2023) 4 - p. 100303 , 2023
Link:
https://doi.org/10.1016/..
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3
What proportion of couples with a history of recurrent preg..:
van Zutven, Laura J. C. M.
;
Mijalkovic, Jona
;
van Veghel-Plandsoen, Monique
...
Molecular Cytogenetics. 16 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1186/..
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4
The role of a multidisciplinary team in managing variants o..:
Diderich, Karin E.M.
;
Klapwijk, Jasmijn E.
;
van der Schoot, Vyne
...
European Journal of Medical Genetics. 66 (2023) 10 - p. 104844 , 2023
Link:
https://doi.org/10.1016/..
?
5
Early onset X‐linked female limited high myopia in three mu..:
Mazijk, Ralph
;
Haarman, Annechien E.G.
;
Hoefsloot, Lies H.
...
Human Mutation. 43 (2022) 3 - p. 380-388 , 2022
Link:
https://doi.org/10.1002/..
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6
High‐yield identification of pathogenicNF1variants by skin ..:
Douben, Hannie C. W.
;
Nellist, Mark
;
van Unen, Leontine
...
Human Mutation. 43 (2022) 12 - p. 2130-2140 , 2022
Link:
https://doi.org/10.1002/..
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7
Whole exome sequencing of known eye genes reveals genetic c..:
Haarman, Annechien E G
;
Thiadens, Alberta A H J
;
van Tienhoven, Marianne
...
Human Molecular Genetics. 31 (2022) 19 - p. 3290-3298 , 2022
Link:
https://doi.org/10.1093/..
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8
Prenatal ultrasound finding of atypical genitalia: Counseli..:
van Bever, Yolande
;
Groenenberg, Irene A. L.
;
Knapen, Maarten F. C. M.
...
Prenatal Diagnosis. 43 (2022) 2 - p. 162-182 , 2022
Link:
https://doi.org/10.1002/..
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9
The potential diagnostic yield of whole exome sequencing in..:
Diderich, Karin E. M.
;
Romijn, Kathleen
;
Joosten, Marieke
...
Acta Obstetricia et Gynecologica Scandinavica. 100 (2020) 6 - p. 1106-1115 , 2020
Link:
https://doi.org/10.1111/..
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10
Novel GAA Variants and Mosaicism in Pompe Disease Identifie..:
in 't Groen, Stijn L.M.
;
de Faria, Douglas O.S.
;
Iuliano, Alessandro
...
Molecular Therapy - Methods & Clinical Development. 17 (2020) - p. 337-348 , 2020
Link:
https://doi.org/10.1016/..
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11
Segmental and total uniparental isodisomy (UPiD) as a disea..:
Labrijn-Marks, Ineke
;
Somers-Bolman, Galhana M.
;
In 't Groen, Stijn L. M.
...
European Journal of Human Genetics. 27 (2019) 6 - p. 919-927 , 2019
Link:
https://doi.org/10.1038/..
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12
Social and medical need for whole genome high resolution NI..:
Srebniak, Malgorzata I.
;
Knapen, Maarten F. C. M.
;
Govaerts, Lutgarde C. P.
...
Molecular Genetics & Genomic Medicine. 8 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1002/..
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13
Holoprosencephaly, orofacial cleft, and frontonaso‐orbital ..:
Richieri‐Costa, Antonio
;
Zechi‐Ceide, Roseli M.
;
Candido‐Souza, Rosana M.
...
American Journal of Medical Genetics Part A. 179 (2019) 11 - p. 2170-2177 , 2019
Link:
https://doi.org/10.1002/..
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14
Placental studies elucidate discrepancies between NIPT show..:
Van Opstal, Diane
;
van Veen, Stefanie
;
Joosten, Marieke
...
Prenatal Diagnosis. 39 (2019) 11 - p. 1016-1025 , 2019
Link:
https://doi.org/10.1002/..
?
15
Mucolipidosis type III, a series of adult patients:
Oussoren, Esmee
;
van Eerd, David
;
Murphy, Elaine
...
Journal of Inherited Metabolic Disease. 41 (2018) 5 - p. 839-848 , 2018
Link:
https://doi.org/10.1007/..
1-15