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Results: 1-25 | 26-33 |
Results: 26-33/33
UNIFORM GENETIC DIAGNOSIS CODE REGISTRATION
Authors: GERAEDTS JPM BIJLSMA MB HENNEKAM FAM LINDHOUT D BEEMER FA BAKKER E KLEIJER WJ DEFRANCE HF DEDIESMULDERS CEM DURAN M VANGENNIP AH VANMENS JT MANTEL G VERHAGE RE ZWAMBORNHANSSEN AMN
Citation: Jpm. Geraedts et al., UNIFORM GENETIC DIAGNOSIS CODE REGISTRATION, American journal of human genetics, 57(4), 1995, pp. 491-491
SYMPTOMATOLOGY OF PATIENTS WITH OLIGODONTIA
Authors: SCHALKVANDERWEIDE Y BEEMER FA FABER JAJ BOSMAN F
Citation: Y. Schalkvanderweide et al., SYMPTOMATOLOGY OF PATIENTS WITH OLIGODONTIA, Journal of oral rehabilitation, 21(3), 1994, pp. 247-261
INTERMITTENT HAIR LOSS IN A CHILD WITH PIBI(D)S-SYNDROME AND TRICHOTHIODYSTROPHY WITH DEFECTIVE-DNA REPAIR XERODERMA-PIGMENTOSUM GROUP-D
Authors: KLEIJER WJ BEEMER FA BOOM BW
Citation: Wj. Kleijer et al., INTERMITTENT HAIR LOSS IN A CHILD WITH PIBI(D)S-SYNDROME AND TRICHOTHIODYSTROPHY WITH DEFECTIVE-DNA REPAIR XERODERMA-PIGMENTOSUM GROUP-D, American journal of medical genetics, 52(2), 1994, pp. 227-230
ADDITIONAL CASE OF OPSISMODYSPLASIA SUPPORTING AUTOSOMAL RECESSIVE INHERITANCE
Authors: BEEMER FA KOZLOWSKI KS
Citation: Fa. Beemer et Ks. Kozlowski, ADDITIONAL CASE OF OPSISMODYSPLASIA SUPPORTING AUTOSOMAL RECESSIVE INHERITANCE, American journal of medical genetics, 49(3), 1994, pp. 344-347
CLINICAL SCREENING AS COMPARED WITH DNA ANALYSIS IN FAMILIES WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A
Authors: LIPS CJM LANDSVATER RM HOPPENER JWM GEERDINK RA BLIJHAM G VANVEEN JMJS VANGILS APG DEWIT MJ ZEWALD RA BERENDS MJH BEEMER FA BROUWERSSMALBRAAK J JANSEN RPM VANAMSTEL HKP VANVROONHOVEN TJM VROOM TM
Citation: Cjm. Lips et al., CLINICAL SCREENING AS COMPARED WITH DNA ANALYSIS IN FAMILIES WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A, The New England journal of medicine, 331(13), 1994, pp. 828-835
REDUCTIONS IN SIZE AND LEFT-RIGHT ASYMMETRY OF TEETH IN HUMAN OLIGODONTIA
Authors: SCHALKVANDERWEIDE Y STEEN WHA BEEMER FA BOSMAN F
Citation: Y. Schalkvanderweide et al., REDUCTIONS IN SIZE AND LEFT-RIGHT ASYMMETRY OF TEETH IN HUMAN OLIGODONTIA, Archives of oral biology, 39(11), 1994, pp. 935-939
PATERNAL DUPLICATION OF CHROMOSOME-5Q11.2-5Q14 IN A MALE BORN WITH CRANIOSTENOSIS, EAR TAGS, KIDNEY DYSPLASIA AND SEVERAL OTHER ANOMALIES
Authors: BRESLAUSIDERIUS EJ WIJNEN JT DAUWERSE JG DEPATER JM BEEMER FA KHAN PM
Citation: Ej. Breslausiderius et al., PATERNAL DUPLICATION OF CHROMOSOME-5Q11.2-5Q14 IN A MALE BORN WITH CRANIOSTENOSIS, EAR TAGS, KIDNEY DYSPLASIA AND SEVERAL OTHER ANOMALIES, Human genetics, 92(5), 1993, pp. 481-485
CYTOPLASMIC CATALASE AND GHOSTLIKE PEROXISOMES IN THE LIVER FROM A CHILD WITH ATYPICAL CHONDRODYSPLASIA PUNCTATA
Authors: ESPEEL M HEIKOOP JC SMEITINK JAM BEEMER FA DECRAEMER D VANDENBERG M HASHIMOTO T WANDERS RJA SCHUTGENS RBH POLLTHE BT ROELS F
Citation: M. Espeel et al., CYTOPLASMIC CATALASE AND GHOSTLIKE PEROXISOMES IN THE LIVER FROM A CHILD WITH ATYPICAL CHONDRODYSPLASIA PUNCTATA, Ultrastructural pathology, 17(6), 1993, pp. 623-636
Risultati: 1-25 | 26-33 |