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Results:
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Results: 8
A FAMILY WITH OSTEOGENESIS IMPERFECTA, FRONTONASAL DYSPLASIA, EAR ABNORMALITY AND MENTAL-RETARDATION
Authors:
CEYLANER G
CEYLANER S
DUNDAR M
Citation: G. Ceylaner et al., A FAMILY WITH OSTEOGENESIS IMPERFECTA, FRONTONASAL DYSPLASIA, EAR ABNORMALITY AND MENTAL-RETARDATION, Journal of Medical Genetics, 34, 1997, pp. 527-527
Authors:
DUNDAR M
CEYLANER S
CEYLANER G
Citation: M. Dundar et al., A CASE WITH MULTIPLE PTERGIUM SYNDROME (ESCOBAR-SYNDROME), Journal of Medical Genetics, 34, 1997, pp. 528-528
Authors:
KURTOGLU S
DUNDAR M
HALLAC IK
UZUM K
OKUMUS Y
OKTEM T
Citation: S. Kurtoglu et al., POLYCYSTIC KIDNEY-DISEASE, BILIARY DYSGENESIS IN A PATIENT WITH LARSENS-SYNDROME, Clinical genetics, 51(6), 1997, pp. 408-411
Authors:
DUNDAR M
DEMIRYILMAZ F
DEMIRYILMAZ I
KUMANDAS S
ERKILIC K
KENDIRCI M
TUNCEL M
OZYAZGAN I
TOLMIE JL
Citation: M. Dundar et al., AN AUTOSOMAL RECESSIVE ADDUCTED THUMB CLUB FOOT SYNDROME OBSERVED IN TURKISH COUSINS, Clinical genetics, 51(1), 1997, pp. 61-64
Authors:
DUNDAR M
ERKILIC K
DEMIRYILMAZ F
KUCUKAYDIN M
KENDIRCI M
OKUR H
KAZEZ A
Citation: M. Dundar et al., CONGENITAL ALACRIMA IN A PATIENT WITH G-(OPITZ-FRIAS)-SYNDROME, Human genetics, 97(4), 1996, pp. 540-542
Authors:
DUNDAR M
LANYON WG
CONNOR JM
Citation: M. Dundar et al., DETECTION OF GERMLINE MUTATIONS IN THE RB1 GENE USING AMPLIFICATION MISMATCH DETECTION (AMD) ANALYSIS AND DIRECT SEQUENCING OF PCR PRODUCTS, Journal of Medical Genetics, 32(2), 1995, pp. 154-155
Authors:
DUNDAR M
LANYON WG
CONNOR JM
Citation: M. Dundar et al., MOLECULAR PATHOLOGY OF THE RB1 GENE IN RETINOBLASTOMA, BREAST AND BLADDER-TUMORS, Journal of Medical Genetics, 32(2), 1995, pp. 155-155
Authors:
DUNDAR M
LANYON WG
CONNOR JM
Citation: M. Dundar et al., SCOTTISH FREQUENCY OF THE COMMON G985 MUTATION IN THE MEDIUM-CHAIN ACYL-COA DEHYDROGENASE (MCAD) GENE AND THE ROLE OF MCAD DEFICIENCY IN SUDDEN-INFANT-DEATH-SYNDROME (SIDS), Journal of inherited metabolic disease, 16(6), 1993, pp. 991-993
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