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Results: 1-9 |
Results: 9
DE-NOVO 7Q36 DELETION - BREAKPOINT ANALYSIS AND TYPES OF HOLOPROSENCEPHALY
Authors: FRINTS SGM SCHOENMAKERS EFPM SMEETS E PETIT P FRYNS JP
Citation: Sgm. Frints et al., DE-NOVO 7Q36 DELETION - BREAKPOINT ANALYSIS AND TYPES OF HOLOPROSENCEPHALY, American journal of medical genetics, 75(2), 1998, pp. 153-158
CLONING OF SUCROSE - SUCROSE 1-FRUCTOSYLTRANSFERASE FROM ONION AND SYNTHESIS OF STRUCTURALLY DEFINED FRUCTAN MOLECULES FROM SUCROSE
Authors: VIJN I VANDIJKEN A LUSCHER M BOS A SMEETS E WEISBEEK P WIEMKEN A SMEEKENS S
Citation: I. Vijn et al., CLONING OF SUCROSE - SUCROSE 1-FRUCTOSYLTRANSFERASE FROM ONION AND SYNTHESIS OF STRUCTURALLY DEFINED FRUCTAN MOLECULES FROM SUCROSE, Plant physiology, 117(4), 1998, pp. 1507-1513
CATAPLEXY IN COFFIN-LOWRY-SYNDROME
Authors: FRYNS JP SMEETS E
Citation: Jp. Fryns et E. Smeets, CATAPLEXY IN COFFIN-LOWRY-SYNDROME, Journal of Medical Genetics, 35(8), 1998, pp. 702-702
WOLF-HIRSCHHORN-SYNDROME WITH CRYPTIC 4P16.3 DELETION AND BALANCED UNBALANCED MOSAICISM IN THE MOTHER (VOL 41, PG 73, 1998)/
Authors: FRYNS JP SMEETS E DEVRIENDT K PETIT P
Citation: Jp. Fryns et al., WOLF-HIRSCHHORN-SYNDROME WITH CRYPTIC 4P16.3 DELETION AND BALANCED UNBALANCED MOSAICISM IN THE MOTHER (VOL 41, PG 73, 1998)/, Annales de genetique, 41(3), 1998, pp. 148-148
WOLF-HIRSCHHORN-SYNDROME WITH CRYPTIC 4P16.3 DELETION AND BALANCED UNBALANCED MOSAICISM IN THE MOTHER/
Authors: FRYNS JP SMEETS E DEVRIENDT K PETIT P
Citation: Jp. Fryns et al., WOLF-HIRSCHHORN-SYNDROME WITH CRYPTIC 4P16.3 DELETION AND BALANCED UNBALANCED MOSAICISM IN THE MOTHER/, Annales de genetique, 41(2), 1998, pp. 73-76
ON THE NOSOLOGY OF THE PRIMARY TRUE MICROCEPHALY, CHORIORETINAL DYSPLASIA, LYMPHEDEMA ASSOCIATION
Authors: FRYNS JP SMEETS E VANDENBERGHE H
Citation: Jp. Fryns et al., ON THE NOSOLOGY OF THE PRIMARY TRUE MICROCEPHALY, CHORIORETINAL DYSPLASIA, LYMPHEDEMA ASSOCIATION, Clinical genetics, 48(3), 1995, pp. 131-133
REGIONAL PROTEUS-SYNDROME AND SOMATIC MOSAICISM
Authors: SMEETS E FRYNS JP COHEN MM
Citation: E. Smeets et al., REGIONAL PROTEUS-SYNDROME AND SOMATIC MOSAICISM, American journal of medical genetics, 51(1), 1994, pp. 29-31
ECTOMORPHIC HABITUS, SEVERE MENTAL-RETARDATION, AND CHARACTERISTIC FACE - A NEW MCA MR SYNDROME/
Authors: FRYNS JP SMEETS E THIRY P GEUTJENS J VINKEN L VANDENBERGHE H
Citation: Jp. Fryns et al., ECTOMORPHIC HABITUS, SEVERE MENTAL-RETARDATION, AND CHARACTERISTIC FACE - A NEW MCA MR SYNDROME/, American journal of medical genetics, 49(1), 1994, pp. 91-93
MELKERSSON-ROSENTHAL SYNDROME AND DE-NOVO AUTOSOMAL T(921)(P11P11) TRANSLOCATION
Authors: SMEETS E FRYNS JP VANDENBERGHE H
Citation: E. Smeets et al., MELKERSSON-ROSENTHAL SYNDROME AND DE-NOVO AUTOSOMAL T(921)(P11P11) TRANSLOCATION, Clinical genetics, 45(6), 1994, pp. 323-324
Risultati: 1-9 |