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American Journal of Medical Genetics|July 15, 1994
Apparently enhanced visual information processing in female fragile X carriers: preliminary findingsJ Steyaert, M Borghgraef, J P FrynsGenetic Counseling (Geneva, Switzerland)|February 26, 2009
A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphismH Peeters, J Vermeesch, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1996
Temperament in Williams syndromeL Plissart, M Borghgraef, J P FrynsJournal De Genetique Humaine|September 1, 1989
On the occurrence of macroorchidism and mental handicap in the Aarskog syndromeJ P Fryns, H Van den BergheAnnales De Genetique|January 1, 1979
Familial paracentric inversion of the short arm of chromosome 3J P Fryns, H van den BergheHuman Genetics|October 1, 1986
8q24.12 Interstitial deletion in trichorhinophalangeal syndrome type IJ P Fryns, H Van den BergheHuman Genetics|January 19, 1979
Langer type of mesomelic dwarfism as the possible homozygous expression of dyschondrosteosisJ P Fryns, H Van Den BergheCellular and Molecular Life Sciences : CMLS|October 2, 2001
Transcription factor GATA3 and the human HDR syndromeH Van Esch, K DevriendtPhysical Review. E|January 20, 2018
Unified mean-field framework for susceptible-infected-susceptible epidemics on networks, based on graph partitioning and the isoperimetric inequalityK Devriendt, P Van MieghemGenetic Counseling (Geneva, Switzerland)|August 2, 2002
Oculo-dento-digital dysplasia (OMIM *164200). Full manifestation of the syndrome in a 9.5 year-old girl and type III syndactyly in the fatherD M Ioan, D Dagomiz, J P FrynsPageof 90