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Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Dysmorphology report: on the association of microcephaly and preaxial polydactyly. Another example of Howard-Young syndromeP Collignon, N Philip, G Simonin, et al.Genetic Counseling (Geneva, Switzerland)|February 19, 2010
Prenatal diagnosis of a de novo supernumerary marker chromosome originating from chromosome 16S Yakut, Z Cetin, M Simşek, et al.Genetic Counseling (Geneva, Switzerland)|February 19, 2010
Fluorescence in situ hybridization and single nucleotide polymorphism of a new case with inv dup del(8p)A O Caglayan, J J M Engelen, S Ghesquiere, et al.Genetic Counseling (Geneva, Switzerland)|February 19, 2010
A provisionally unique syndrome with features including "molar tooth" sign and "femoral hypoplasia"A O Caglayan, H Gumus, A Yikilmaz, et al.Genetic Counseling (Geneva, Switzerland)|February 19, 2010
A prenatally sonographically diagnosed conotruncal anomaly with mosaic type trisomy 21 and 22q11.2 microdeletion/DiGeorge syndromeS Balci, F S Altugan, D Alehan, et al.Genetic Counseling (Geneva, Switzerland)|February 19, 2010
Report of a girl with vacterl syndrome and right pulmonary agenesisS Avcu, C Akgun, H Temel, et al.Genetic 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)|April 30, 2009
Deletion of Xpter encompassing the SHOX gene and PAR1 region in familial patients with Leri-Weill Dyschondrosteosis syndromeL Mutesa, J F Vanbellinghen, A C Hellin, et al.Genetic Counseling (Geneva, Switzerland)|April 30, 2009
Mutations of the noggin (NOG) and of the activin A type I receptor (ACVR1) genes in a series of twenty-seven French fibrodysplasia ossificans progressiva (FOP) patientsG Lucotte, A Houzet, C Hubans, et al.Genetic Counseling (Geneva, Switzerland)|April 23, 2005
De novo deletion 7q36 resulting from a distal 7q/8q translocation: phenotypic expression and comparison to the literatureT Lukusa, J R Vermeesch, J P FrynsPageof 116