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J P Fryns
Observed name:
J-P FRYNS
OpenAlex ID:
A5113481554
Hyperacusis in Williams syndrome: a sample survey study.
1997
·
J Van Borsel
, L M Curfs
, et al.
·
PubMed
·
60
New MR/MCA syndrome with distinct facial appearance and general habitus, broad and webbed neck, hypoplastic inverted nipples, epilepsy, and pachygyria of the frontal lobes
2000
·
J-P FRYNS
, S AFTIMOS
·
Journal of Medical Genetics
·
24
PDF
Hereditary motor and sensory neuropathy (HMSN) IA, developmental delay and autism related disorder in a boy with duplication (17)(p11.2p12).
2004
·
U Moog
, J J Engelen
, et al.
·
PubMed
·
17
Second polar body inclusion results in diploid/triploid mixoploidy.
2003
·
H Brems
, A Vogels
, et al.
·
PubMed
·
8
Abnormal first trimester screen in partial deletion of chromosome 6p21: a case-report.
2007
·
M H Hulsbergen
, S G K Van Calenbergh
, et al.
·
PubMed
·
5
Eet- en spraakstoornissen bij patiënten met het velo-cardio-faciaal syndroom
1999
·
Nathalie Rommel
, G. Vantrappen
, et al.
DNA diagnostiek en mucoviscidose. Waar staan we vijf jaar na de idenficatie van het mucoviscidosegen
1995
·
K Devriendt
, Harry Cuppens
, et al.
·
Tijdschrift voor Geneeskunde
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Works count:
7
Citation count:
114
H-index:
5
I10-index:
3
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