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Genetic Counseling (Geneva, Switzerland)|January 1, 1991
Lobar holoprosencephaly and Xq22 deletionP Petit, P Moerman, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1991
Pre- and postnatal growth retardation--severe mental retardation--acral limb deficiencies with poorly keratinized nails. Another example of a distinct syndrome of inherited intrauterine dwarfism?J Cartwright, M Nelson, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1991
The fetal phenotype of partial trisomy of the long arm of chromosome 4 (4q22----4qter)P Petit, P Moerman, J P FrynsAmerican Journal of Medical Genetics|May 1, 1988
The concurrence of Klinefelter syndrome and fragile X syndromeJ P Fryns, H Van den BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1992
Smith-Lemli-Opitz syndrome: the changing phenotype with ageC de Die-Smulders, J P FrynsAmerican Journal of Medical Genetics|December 26, 2001
Unusual chromosomal mosaicism in Wolf-Hirschhorn syndrome: del(4)(p16)/der(4)(qter-q31.3::pter-qter)M Syrrou, M Borghgraef, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1995
Costello syndrome: the natural history of a true postnatal growth retardation syndromeS Umans, P Decock, J P FrynsGenetic Counseling (Geneva, Switzerland)|April 29, 1998
Diaphragmatic hernia in the Coffin-Siris syndromeV Delvaux, P Moerman, J P FrynsAnnales De Genetique|January 1, 1980
Partial duplication of the long arm of chromosome 4J P Fryns, H van den BerghePageof 90