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Results: 1-7 |
Results: 7
MUTATION ANALYSIS FOR PRENATAL-DIAGNOSIS OF HEREDITARY TYROSINEMIA TYPE-1
Authors: MUSTONEN A VANAMSTEL HKP BERGER R SALO MK VIINIKKA L SIMOLA KOJ
Citation: A. Mustonen et al., MUTATION ANALYSIS FOR PRENATAL-DIAGNOSIS OF HEREDITARY TYROSINEMIA TYPE-1, Prenatal diagnosis, 17(10), 1997, pp. 964-966
APPLICABILITY OF A CHECKLIST FOR CLINICAL SCREENING OF THE FRAGILE-X-SYNDROME
Authors: ARVIO M PEIPPO M SIMOLA KOJ
Citation: M. Arvio et al., APPLICABILITY OF A CHECKLIST FOR CLINICAL SCREENING OF THE FRAGILE-X-SYNDROME, Clinical genetics, 52(4), 1997, pp. 211-215
USHERS SYNDROME TYPE-3 IN FINLAND
Authors: PAKARINEN L KARJALAINEN S SIMOLA KOJ LAIPPALA P KAITALO H
Citation: L. Pakarinen et al., USHERS SYNDROME TYPE-3 IN FINLAND, The Laryngoscope, 105(6), 1995, pp. 613-617
CLINICAL-FEATURES OF 9 MALES WITH MOLECULARLY DEFINED DELETIONS OF THE Y-CHROMOSOME LONG ARM
Authors: SALO P IGNATIUS J SIMOLA KOJ TAHVANAINEN E KAARIAINEN H
Citation: P. Salo et al., CLINICAL-FEATURES OF 9 MALES WITH MOLECULARLY DEFINED DELETIONS OF THE Y-CHROMOSOME LONG ARM, Journal of Medical Genetics, 32(9), 1995, pp. 711-715
THE 48,XXYY SYNDROME - A CASE DETECTED BY MATERNAL SERUM ALPHA-FETOPROTEIN SCREENING
Authors: NYBERG RH KARHU R KARIKOSKI R SIMOLA KOJ
Citation: Rh. Nyberg et al., THE 48,XXYY SYNDROME - A CASE DETECTED BY MATERNAL SERUM ALPHA-FETOPROTEIN SCREENING, Prenatal diagnosis, 14(7), 1994, pp. 644-645
X-LINKED LATERALITY SEQUENCE IN A FAMILY WITH CARRIER MANIFESTATIONS
Authors: MIKKILA SP JANAS M KARIKOSKI R TARKKILA T SIMOLA KOJ
Citation: Sp. Mikkila et al., X-LINKED LATERALITY SEQUENCE IN A FAMILY WITH CARRIER MANIFESTATIONS, American journal of medical genetics, 49(4), 1994, pp. 435-438
GENETIC-LINKAGE STUDIES IN USHER SYNDROME TYPE-3
Authors: SANKILA EM PAKARINEN L SIMOLA KOJ KAARIAINEN H DELACHAPELLE A
Citation: Em. Sankila et al., GENETIC-LINKAGE STUDIES IN USHER SYNDROME TYPE-3, American journal of human genetics, 53(3), 1993, pp. 1712-1712
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