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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
The fetal phenotype of partial trisomy of the long arm of chromosome 4 (4q22----4qter)P Petit, P Moerman, J P FrynsClinical Genetics|April 1, 1984
Severe limb malformations in 4p deletionM Haspeslagh, J P Fryns, P MoermanGenetic Counseling (Geneva, Switzerland)|October 24, 2000
Prenatal echographic diagnosis of laryngeal atresia as part of a multiple congenital anomalies (MCA) syndromeI Witters, P Moerman, J P FrynsAmerican Journal of Medical Genetics|February 1, 1992
Acrofacial dysostosis syndrome type Rodriguez: a new lethal MCA syndromeP Petit, P Moerman, J P FrynsClinical Genetics|April 1, 1992
Full 69,XXY triploidy and sex-reversal: a further example of true hermaphrodism associated with multiple malformationsP Petit, P Moerman, J P FrynsJournal De Genetique Humaine|June 1, 1984
[Prune belly syndrome, a secondary urethral functional obstruction due to prostatic hypoplasia]P Moerman, J P Fryns, P GoodeerisGenetic Counseling (Geneva, Switzerland)|January 1, 1996
Caudal developmental field defect with female pseudohermaphroditism and VACTERL anomaliesT Lukusa, P Moerman, J P FrynsGenetic Counseling (Geneva, Switzerland)|April 29, 1998
Diaphragmatic hernia in the Coffin-Siris syndromeV Delvaux, P Moerman, J P FrynsGenetic Counseling (Geneva, Switzerland)|November 6, 2001
Further evidence for germinal mosaicism in cleft hand/cleft foot syndrome. Two affected halfsisters and normal fatherL De Smet, K Devriendt, J P FrynsPageof 105