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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
CLINICAL FINDINGS WITH IMPLICATIONS FOR GENETIC TESTING IN FAMILIES WITH CLUSTERING OF COLORECTAL-CANCER
Authors: WIJNEN JT VASEN HFA KHAN PM ZWINDERMAN AH VANDERKLIFT H MULDER A TOPS C MOLLER P FODDE R MENKO F TAAL B NAGENGAST F BRUNNER H KLEIBEUKER J SIJMONS R GRIFFIOEN G BROCKERVRIENDS A BAKKER E VANLEEUWENCORNELISSE I MEIJERSHEIJBOER A LINDHOUT D BREUNING M POST J SCHAAP C APOLD J HEIMDAL K BERTARIO L BISGAARD ML GOETZ P
Citation: Jt. Wijnen et al., CLINICAL FINDINGS WITH IMPLICATIONS FOR GENETIC TESTING IN FAMILIES WITH CLUSTERING OF COLORECTAL-CANCER, The New England journal of medicine, 339(8), 1998, pp. 511-518
THE PREVENTION OF RELATIONSHIP DISTRESS FOR COUPLES AT RISK - A CONTROLLED EVALUATION WITH 9-MONTH AND 2-YEAR FOLLOW-UPS
Authors: VANWIDENFELT B HOSMAN C SCHAAP C VANDERSTAAK C
Citation: B. Vanwidenfelt et al., THE PREVENTION OF RELATIONSHIP DISTRESS FOR COUPLES AT RISK - A CONTROLLED EVALUATION WITH 9-MONTH AND 2-YEAR FOLLOW-UPS, Family relations, 45(2), 1996, pp. 156-165
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
FAMILIAL MEDULLARY-THYROID CARCINOMA - NOT A DISTINCT ENTITY - GENOTYPE-PHENOTYPE CORRELATION IN A LARGE FAMILY
Authors: MOERS AMJ LANDSVATER RM SCHAAP C VANVEEN JMJS DEVALK IAJ BLIJHAM GH HOPPENER JWM VROOM TM VANAMSTEL HKP LIPS CJM
Citation: Amj. Moers et al., FAMILIAL MEDULLARY-THYROID CARCINOMA - NOT A DISTINCT ENTITY - GENOTYPE-PHENOTYPE CORRELATION IN A LARGE FAMILY, The American journal of medicine, 101(6), 1996, pp. 635-641
RECURRENCE OF DIGEORGE-SYNDROME - PRENATAL DETECTION BY FISH OF A MOLECULAR 22Q11 DELETION
Authors: VANHEMEL JO SCHAAP C VANOPSTAL D MULDER MP NIERMEIJER MF MEIJERS JHC
Citation: Jo. Vanhemel et al., RECURRENCE OF DIGEORGE-SYNDROME - PRENATAL DETECTION BY FISH OF A MOLECULAR 22Q11 DELETION, Journal of Medical Genetics, 32(8), 1995, pp. 657-658
SEVERE PROGRESSIVE NEUROLOGICAL DISORDER ASSOCIATED WITH HYDROCEPHALUS IN A MAN WITH FRAGILE-X-SYNDROME
Authors: SCHAAP C FRYNS JP
Citation: C. Schaap et Jp. Fryns, SEVERE PROGRESSIVE NEUROLOGICAL DISORDER ASSOCIATED WITH HYDROCEPHALUS IN A MAN WITH FRAGILE-X-SYNDROME, American journal of medical genetics, 51(4), 1994, pp. 403-404
FAMILY-THERAPY AND PSYCHOPATHOLOGY - DEVELOPMENTS IN RESEARCH AND APPROACHES TO TREATMENT
Authors: LANGE A SCHAAP C VANWIDENFELT B
Citation: A. Lange et al., FAMILY-THERAPY AND PSYCHOPATHOLOGY - DEVELOPMENTS IN RESEARCH AND APPROACHES TO TREATMENT, Journal of family therapy, 15(2), 1993, pp. 113-146
THE HETEROGENEITY OF SCHIZOPHRENIC INFORMATION-PROCESSING AND NEGATIVE VERSUS POSITIVE SYMPTOMS
Authors: VERBRAAK MJPM HOOGDUIN CAL SCHAAP C
Citation: Mjpm. Verbraak et al., THE HETEROGENEITY OF SCHIZOPHRENIC INFORMATION-PROCESSING AND NEGATIVE VERSUS POSITIVE SYMPTOMS, The Journal of nervous and mental disease, 181(12), 1993, pp. 738-743
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