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Genetic Counseling (Geneva, Switzerland)|July 16, 2008
Prenatal diagnosis of trisomy 21: registration results from a single genetic centerI Witters, J P FrynsJournal De Genetique Humaine|June 1, 1985
[Polycystic renal diseases: morphology and genetic counseling]P Moerman, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1990
Wolf-Hirschhorn and Cri du Chat syndromes resulting from familial translocations: 3 further examples of the Bp monosomy epistatic effectP Petit, J P FrynsAmerican Journal of Medical Genetics|January 8, 1999
Syndrome of facial, oral, and digital anomalies due to 7q21.2-->q22.1 duplicationT Lukusa, J P FrynsGenetic Counseling (Geneva, Switzerland)|August 2, 2002
The velocardiofacial syndrome: a reviewA Vogels, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1997
Interstitial deletion 2p accompanied by marker chromosome formation of the deleted segment resulting in a stable acentric marker chromosomeP Petit, J P FrynsGenetic Counseling (Geneva, Switzerland)|April 29, 1998
Oral-facial-digital syndrome type IV (Mohr-Majewski syndrome): a fetopathological studyP Moerman, J P FrynsBiochimica Et Biophysica Acta|November 3, 2007
WITHDRAWN: Human chromosome fragilityT Lukusa, J P FrynsJournal of Medical Genetics|April 1, 1993
Short limbed dwarfism, genital hypoplasia, sparse hair, and vertebral anomalies: a variant of Ellis-van Creveld syndrome?J P Fryns, P MoermanClinical Genetics|December 1, 1985
The Fryns syndrome: diaphragmatic defects, craniofacial dysmorphism, and distal digital hypoplasia. Further evidence for autosomal recessive inheritanceP Meinecke, J P FrynsPageof 90