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Journal of Medical Genetics|July 1, 1988
Unknown syndrome: abnormal facies, hypothyroidism, and severe retardation: a second patientJ P Fryns, P MoermanGenetic Counseling (Geneva, Switzerland)|January 1, 1992
Laryngeal atresia sequence as part of the DiGeorge developmental field defectP Moerman, F de Zegher, K Vandenberghe, et al.Journal of Medical Genetics|March 1, 1996
Mental retardation, distinct craniofacial dysmorphism, and central nervous system malformation: confirmation of a syndromeK Devriendt, L D'Espallier, J P FrynsAmerican Journal of Medical Genetics|March 1, 1996
Progressive extrapyramidal disorder with primary hypogonadism and alopecia in sibs: a new syndrome?K Devriendt, E Legius, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1996
Macrocephaly, hypospadias grade III-IV, and fragile X-like behavior in identical twins without involvement of the FMR-1 geneJ P Fryns, M D'Hooghe, K DevriendtAnnales De Genetique|August 6, 1999
A 3p deletion syndrome in a child with both del(3)(p25-->pter) and dup(17)(q23-->qter)T Lukusa, K Devriendt, J P FrynsClinical Genetics|July 11, 1998
Deletion in chromosome region 22q11 in a child with CHARGE associationK Devriendt, A Swillen, J P FrynsGenetic Counseling (Geneva, Switzerland)|October 20, 1998
Further delineation of the KBG syndromeK Devriendt, M Holvoet, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1993
Nager acrofacial dysostosis and preaxial polydactyly: a further example with lethal outcomeP Petit, P Moerman, J P FrynsPageof 105