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Prenatal Diagnosis|April 1, 1992
Evaluation of prenatal diagnosis by a registry of congenital anomaliesC Stoll, Y Alembik, B Dott, et al.Archives Francaises De Pediatrie|October 1, 1991
[Congenital malformations in a series of 131,760 consecutive births during 10 years]C Stoll, B Dott, Y Alembik, et al.Pediatric Nephrology (Berlin, Germany)|July 1, 1990
Risk factors in internal urinary system malformationsC Stoll, Y Alembik, M P Roth, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Rett-like syndrome in fragile X syndromeY Alembik, B Dott, C StollAnnales De Genetique|December 9, 2003
Limb reduction defects in the first generation and deafness in the second generation of intrauterine exposed fetuses to diethylstilbestrolC Stoll, Y Alembik, B DottGenetic Counseling (Geneva, Switzerland)|August 23, 2007
Associated malformations in cases with neural tube defectsC Stoll, Y Alembik, B DottAnnales De Genetique|October 20, 1999
Familial coarctation of the aorta in three generationsC Stoll, Y Alembik, B DottGenetic Counseling (Geneva, Switzerland)|April 29, 1998
Oligodontia, microcephaly and facial dysmorphia syndromeC Stoll, B Dott, Y AlembikAnnales De Genetique|May 26, 1998
Impact of routine fetal ultrasonographic screening on the prevalence of Down syndrome in non aged mothersC Stoll, Y Alembik, B DottGenetic Counseling (Geneva, Switzerland)|January 1, 1995
Complex congenital heart disease, microcephaly, pheochromocytoma and neurofibromatosis type I in a girl born from consanguineous parentsC Stoll, Y Alembik, B DottPageof 33