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Clinical Genetics|April 1, 1984
Severe limb malformations in 4p deletionM Haspeslagh, J P Fryns, P MoermanGenetic Counseling (Geneva, Switzerland)|April 29, 1998
Diaphragmatic hernia in the Coffin-Siris syndromeV Delvaux, P Moerman, J P FrynsGenetic 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)|January 1, 1996
Variable expression of phenotype in offspring with partial monosomy 7q and partial trisomy 8p in a family with a rcp (7;8)(134;p12) translocationS G Frints, P Moerman, J P FrynsEuropean Journal of Obstetrics, Gynecology, and Reproductive Biology|April 16, 1991
Abdominal distension as the first echographic sign of hydrometrocolpos in a female fetusP Petit, D Thomas, P Moerman, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Catel-Manzke palatodigital syndrome in a second trimester female foetus with nuchal oedema, costovertebral anomalies and radial ray defectP Petit, P Moerman, E Legius, et al.Pageof 89