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Results: 1-9 |
Results: 9
PHENOTYPIC OVERLAP BETWEEN MCKUSICK-KAUFMAN AND BARDET-BIEDL SYNDROMES - ARE THEY RELATED
Authors: SCHAAP C TENTUSSCHER MPM SCHRANDER JJP KUIJTEN RH SCHRANDERSTUMPEL CTRM
Citation: C. Schaap et al., PHENOTYPIC OVERLAP BETWEEN MCKUSICK-KAUFMAN AND BARDET-BIEDL SYNDROMES - ARE THEY RELATED, European journal of pediatrics, 157(2), 1998, pp. 170-171
WHATS IN A NAME
Authors: SCHRANDERSTUMPEL CTRM
Citation: Ctrm. Schranderstumpel, WHATS IN A NAME, American journal of medical genetics, 79(3), 1998, pp. 228-228
SIBS WITH AXENFELD-RIEGER ANOMALY, HYDROCEPHALUS, AND LEPTOMENINGEAL CALCIFICATIONS - A NEW AUTOSOMAL RECESSIVE SYNDROME
Authors: MOOG U BLEEKERWAGEMAKERS EM CROBACH P VLES JSH SCHRANDERSTUMPEL CTRM
Citation: U. Moog et al., SIBS WITH AXENFELD-RIEGER ANOMALY, HYDROCEPHALUS, AND LEPTOMENINGEAL CALCIFICATIONS - A NEW AUTOSOMAL RECESSIVE SYNDROME, American journal of medical genetics, 78(3), 1998, pp. 263-266
FAMILIAL CYLINDROMATOSIS MIMICKING TUBEROUS SCLEROSIS COMPLEX AND CONFIRMATION OF THE CYLINDROMATOSIS LOCUS, CYLD1, IN A LARGE FAMILY
Authors: VERHOEF S SCHRANDERSTUMPEL CTRM VUZEVSKI VD TEMPELAARS A JANSEN LAJ MALFEYT GAM CEELEN TL LINDHOUT D HALLEY DJJ VANDENOUWELAND AMW
Citation: S. Verhoef et al., FAMILIAL CYLINDROMATOSIS MIMICKING TUBEROUS SCLEROSIS COMPLEX AND CONFIRMATION OF THE CYLINDROMATOSIS LOCUS, CYLD1, IN A LARGE FAMILY, Journal of Medical Genetics, 35(10), 1998, pp. 841-845
A GENETIC DIAGNOSTIC SURVEY IN AN INSTITUTIONALIZED POPULATION OF 116MODERATELY TO SEVERELY RETARDED PATIENTS
Authors: SCHAAP C SCHRANDERSTUMPEL CTRM COLLAPIJKELS E VANDRIESSCHE J KUSTERS R FRYNS JP
Citation: C. Schaap et al., A GENETIC DIAGNOSTIC SURVEY IN AN INSTITUTIONALIZED POPULATION OF 116MODERATELY TO SEVERELY RETARDED PATIENTS, American journal of medical genetics, 64(1), 1996, pp. 16-16
DELETION OF THE LONG ARM OF CHROMOSOME-6 - 2 NEW PATIENTS AND LITERATURE-REVIEW
Authors: EVERS LJM SCHRANDERSTUMPEL CTRM ENGELEN JJM HOORNTJE TM PULLESHEINTZBERGER CFM SCHRANDER JJP ALBRECHTS JCM PETERS J FRYNS JP
Citation: Ljm. Evers et al., DELETION OF THE LONG ARM OF CHROMOSOME-6 - 2 NEW PATIENTS AND LITERATURE-REVIEW, Clinical genetics, 50(3), 1996, pp. 138-144
CLINICAL FOLLOW-UP OF A GIRL WITH MENTAL-RETARDATION WITH PTERYGIA, SHORTNESS AND DISTINCT FACIAL APPEARANCE (HASPESLAGH SYNDROME)
Authors: SCHRANDERSTUMPEL CTRM PULLESHEINTZBERGER CFM FRYNS JP
Citation: Ctrm. Schranderstumpel et al., CLINICAL FOLLOW-UP OF A GIRL WITH MENTAL-RETARDATION WITH PTERYGIA, SHORTNESS AND DISTINCT FACIAL APPEARANCE (HASPESLAGH SYNDROME), Clinical genetics, 47(6), 1995, pp. 332-334
MOSAIC TETRASOMY 8P IN 2 PATIENTS - CLINICAL-DATA AND REVIEW OF THE LITERATURE
Authors: SCHRANDERSTUMPEL CTRM GOVAERTS CP ENGELEN JJM VANDERBLIJPHILIPSEN M BORGHGRAEF M LOOTS WJG PETERS JJM RIJNVOS WPM SMEETS DFCM FRYNS JP
Citation: Ctrm. Schranderstumpel et al., MOSAIC TETRASOMY 8P IN 2 PATIENTS - CLINICAL-DATA AND REVIEW OF THE LITERATURE, American journal of medical genetics, 50(4), 1994, pp. 377-380
COWS MILK PROTEIN INTOLERANCE IN INFANTS UNDER 1-YEAR-OF-AGE - A PROSPECTIVE EPIDEMIOLOGIC-STUDY
Authors: SCHRANDER JJP VANDENBOGAR JPH FORGET PP SCHRANDERSTUMPEL CTRM KUIJTEN RH KESTER ADM
Citation: Jjp. Schrander et al., COWS MILK PROTEIN INTOLERANCE IN INFANTS UNDER 1-YEAR-OF-AGE - A PROSPECTIVE EPIDEMIOLOGIC-STUDY, European journal of pediatrics, 152(8), 1993, pp. 640-644
Risultati: 1-9 |