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Results: 1-11 |
Results: 11
Pallister-Hall syndrome with stenosis of the cricoid cartilage and microphallus without hypopituitarism
Authors: Stoll, C Martin, AD Donato, L Alembik, Y Sauvage, P Messer, J
Citation: C. Stoll et al., Pallister-Hall syndrome with stenosis of the cricoid cartilage and microphallus without hypopituitarism, GEN COUNSEL, 12(3), 2001, pp. 231-235
Severe hypernatremic dehydration in an infant with Netherton syndrome
Authors: Stoll, C Alembik, Y Tchomakov, D Messer, J Heid, E Boehm, N Calvas, P Hovnanian, A
Citation: C. Stoll et al., Severe hypernatremic dehydration in an infant with Netherton syndrome, GEN COUNSEL, 12(3), 2001, pp. 237-243
Associated malformations in cases with oral clefts
Authors: Stoll, C Alembik, Y Dott, B Roth, MP
Citation: C. Stoll et al., Associated malformations in cases with oral clefts, CLEF PAL-CR, 37(1), 2000, pp. 41-47
Evaluation of prenatal diagnosis of cleft lip/palate by foetal ultrasonographic examination
Authors: Stoll, C Dott, B Alembik, Y Roth, MP
Citation: C. Stoll et al., Evaluation of prenatal diagnosis of cleft lip/palate by foetal ultrasonographic examination, ANN GENET, 43(1), 2000, pp. 11-14
Maternal trace elements, vitamin B12, vitamin A, folic acid, and fetal malformations
Authors: Stoll, C Dott, B Alembik, Y Koehl, C
Citation: C. Stoll et al., Maternal trace elements, vitamin B12, vitamin A, folic acid, and fetal malformations, REPROD TOX, 13(1), 1999, pp. 53-57
Schinzel-Giedion syndrome with severe deafness and neurodegenerative process
Authors: Alembik, Y Christmann, D De Saint Martin, A Eliot, M Dollfus, H Pauly, F Stoll, C
Citation: Y. Alembik et al., Schinzel-Giedion syndrome with severe deafness and neurodegenerative process, ANN GENET, 42(4), 1999, pp. 225-230
Parental consanguinity as a cause for increased incidence of births defects in a study of 238,942 consecutive births
Authors: Stoll, C Alembik, Y Roth, MP Dott, B
Citation: C. Stoll et al., Parental consanguinity as a cause for increased incidence of births defects in a study of 238,942 consecutive births, ANN GENET, 42(3), 1999, pp. 133-139
Familial coarctation of the aorta in three generations
Authors: Stoll, C Alembik, Y Dott, B
Citation: C. Stoll et al., Familial coarctation of the aorta in three generations, ANN GENET, 42(3), 1999, pp. 174-176
Growth curves of children with Down syndrome
Authors: Toledo, C Alembik, Y Jaime, AA Stoll, C
Citation: C. Toledo et al., Growth curves of children with Down syndrome, ANN GENET, 42(2), 1999, pp. 81-90
Congenital anomalies associated with congenital hypothyroidism
Authors: Stoll, C Dott, B Alembik, Y Koehl, C
Citation: C. Stoll et al., Congenital anomalies associated with congenital hypothyroidism, ANN GENET, 42(1), 1999, pp. 17-20
A patient with 13q-syndrome with mild mental retardation and with growth retardation.
Authors: Stoll, C Alembik, Y
Citation: C. Stoll et Y. Alembik, A patient with 13q-syndrome with mild mental retardation and with growth retardation., ANN GENET, 41(4), 1998, pp. 209-212
Risultati: 1-11 |