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Table of contents of journal: *Clinical genetics

Results: 1-25/1026

Authors: MORRISON PJ
Citation: Pj. Morrison, GENETIC TESTING AND INSURANCE IN THE UNITED-KINGDOM, Clinical genetics, 54(5), 1998, pp. 375-379

Authors: BUTLER MG HEDGES L HOVIS CL FEURER ID
Citation: Mg. Butler et al., GENETIC-VARIANTS OF THE HUMAN OBESITY (OB) GENE IN SUBJECTS WITH AND WITHOUT PRADER-WILLI-SYNDROME - COMPARISON WITH BODY-MASS INDEX AND WEIGHT, Clinical genetics, 54(5), 1998, pp. 385-393

Authors: HEGELE RA HARRIS SB CONNELLY PW HANLEY AJG TSUI LC ZINMAN B SCHERER SW
Citation: Ra. Hegele et al., GENETIC-VARIATION IN PARAOXONASE-2 IS ASSOCIATED WITH VARIATION IN PLASMA-LIPOPROTEINS IN CANADIAN OJI-CREE, Clinical genetics, 54(5), 1998, pp. 394-399

Authors: BUENO AL RAMOS FJ BUENO O OLIVARES JL BELLO ML BUENO M
Citation: Al. Bueno et al., SEVERE MALFORMATIONS IN MALES FROM FAMILIES WITH OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS, Clinical genetics, 54(5), 1998, pp. 400-405

Authors: PETEK E KROISEL PM WAGNER K
Citation: E. Petek et al., ISOLATION OF A 370 KB YAC FRAGMENT SPANNING A TRANSLOCATION BREAKPOINT AT 3P14.1 ASSOCIATED WITH HOLOPROSENCEPHALY, Clinical genetics, 54(5), 1998, pp. 406-412

Authors: KING PH WALDROP R LUPSKI JR SHAFFER LG
Citation: Ph. King et al., CHARCOT-MARIE-TOOTH PHENOTYPE PRODUCED BY A DUPLICATED PMP22 GENE AS PART OF A 17P TRISOMY-TRANSLOCATION TO THE X-CHROMOSOME, Clinical genetics, 54(5), 1998, pp. 413-416

Authors: ANGLE B HERSH JH CHRISTENSEN KM
Citation: B. Angle et al., MOLECULARLY PROVEN HYPOCHONDROPLASIA WITH CLOVERLEAF SKULL DEFORMITY - A NOVEL ASSOCIATION, Clinical genetics, 54(5), 1998, pp. 417-420

Authors: KULHARYA AS GARCIAHERAS J RADTKE HB NORRIS KS KEPPEN LD FLANNERY DB
Citation: As. Kulharya et al., PRENATAL-DIAGNOSIS OF A TRISOMY 17P DERIVED FROM A DE-NOVO NON-MOSAICSATELLITED MARKER, Clinical genetics, 54(5), 1998, pp. 421-425

Authors: YAQOOB M CNATTINGIUS S JALIL F ZAMAN S ISELIUS L GUSTAVSON KH
Citation: M. Yaqoob et al., RISK-FACTORS FOR MORTALITY IN YOUNG-CHILDREN LIVING UNDER VARIOUS SOCIOECONOMIC CONDITIONS IN LAHORE, PAKISTAN - WITH PARTICULAR REFERENCE TO INBREEDING, Clinical genetics, 54(5), 1998, pp. 426-434

Authors: GIWERCMAN YL XU C ARVER S POUSETTE A RENELAND R LITHELL H WEDELL A
Citation: Yl. Giwercman et al., NO ASSOCIATION BETWEEN THE ANDROGEN RECEPTOR GENE CAG REPEAT AND IMPAIRED SPERM PRODUCTION IN SWEDISH MEN, Clinical genetics, 54(5), 1998, pp. 435-436

Authors: CARTAULT F STEFFANN J VIDAUD D BOUSQUET S LESURE F RENOUIL M MCDONNELL N FEINGOLD J BELDJORD C BIENVENU T
Citation: F. Cartault et al., DETECTION OF MORE THAN 91-PERCENT CYSTIC-FIBROSIS MUTATIONS IN A SAMPLE OF THE POPULATION FROM REUNION-ISLAND AND IDENTIFICATION OF 2 NOVELMUTATIONS (A309G, S1255L) AND ONE NOVEL POLYMORPHISM (L49L), Clinical genetics, 54(5), 1998, pp. 437-439

Authors: BALCI S KAYIKCIOGLU A DAGLI AS
Citation: S. Balci et al., 2 BROTHERS WITH HYPOSPADIAS, HYPERTELORISM, UPPER LID COLOBOMA AND MIXED-TYPE HEARING-LOSS - A NEW SYNDROME, Clinical genetics, 54(5), 1998, pp. 440-442

Authors: JONES KJ NORTH KN
Citation: Kj. Jones et Kn. North, DEVELOPMENTAL DELAY, EXPRESSIVE APHASIA, HYPOTONIA AND DYSMORPHISM IN2 BROTHERS - AN X-LINKED MENTAL-RETARDATION SYNDROME, Clinical genetics, 54(5), 1998, pp. 443-445

Authors: GASSER T
Citation: T. Gasser, GENETICS OF PARKINSONS-DISEASE, Clinical genetics, 54(4), 1998, pp. 259-265

Authors: VANHEYNINGEN V
Citation: V. Vanheyningen, DEVELOPMENTAL EYE DISEASE - A GENOME ERA PARADIGM, Clinical genetics, 54(4), 1998, pp. 272-282

Authors: CHUDLEY AE
Citation: Ae. Chudley, GENETIC LANDMARKS THROUGH PHILATELY - THE HABSBURG JAW, Clinical genetics, 54(4), 1998, pp. 283-284

Authors: FROSSARD PM HILL SH ELSHAHAT YI OBINECHE EN BOKHARI AM LESTRINGANT GG JOHN A ABDULLE AM
Citation: Pm. Frossard et al., ASSOCIATIONS OF ANGIOTENSINOGEN GENE-MUTATIONS WITH HYPERTENSION AND MYOCARDIAL-INFARCTION IN A GULF POPULATION, Clinical genetics, 54(4), 1998, pp. 285-293

Authors: CHIESA J HOFFET M ROUSSEAU O BOURGEOIS JM SARDA P MARES P BUREAU JP
Citation: J. Chiesa et al., PALLISTER-KILLIAN-SYNDROME [I(12P)] - FIRST PRENATAL-DIAGNOSIS USING CORDOCENTESIS IN THE 2ND-TRIMESTER CONFIRMED BY IN-SITU HYBRIDIZATION, Clinical genetics, 54(4), 1998, pp. 294-302

Authors: FRIDMAN C VARELA MC NICHOLLS RD KOIFFMANN CP
Citation: C. Fridman et al., UNUSUAL CLINICAL-FEATURES IN AN ANGELMAN-SYNDROME PATIENT WITH UNIPARENTAL DISOMY DUE TO A TRANSLOCATION 15Q15Q, Clinical genetics, 54(4), 1998, pp. 303-308

Authors: RUSSO S BRISCIOLI V COGLIATI F MACCHI M LALATTA F LARIZZA L
Citation: S. Russo et al., AN UNUSUAL FRAGILE-X SIBSHIP - FEMALE COMPOUND HETEROZYGOTE AND MALE WITH A PARTIALLY METHYLATED FULL MUTATION, Clinical genetics, 54(4), 1998, pp. 309-314

Authors: DECRECCHIO G SIMONELLI F NUNZIATA G MAZZEO S GRECO GM RINALDI E VENTRUTO V CICCODICOLA A MIANO MG TESTA F CURCI A DURSO M RINALDI MM CAVALIERE ML CASTELLUCCIO P
Citation: G. Decrecchio et al., AUTOSOMAL RECESSIVE FAMILIAL EXUDATIVE VITREORETINOPATHY - EVIDENCE FOR GENETIC-HETEROGENEITY, Clinical genetics, 54(4), 1998, pp. 315-320

Authors: LISKER R CARNEVALE A VILLA JA ARMENDARES S WERTZ DC
Citation: R. Lisker et al., MEXICAN GENETICISTS OPINIONS ON DISCLOSURE ISSUES, Clinical genetics, 54(4), 1998, pp. 321-329

Authors: FRIZELL ER SUTPHEN R DIAMOND FB SHERWOOD M OVERHAUSER J
Citation: Er. Frizell et al., T(1-18)(Q32.1-Q22.1) ASSOCIATED WITH GENITOURINARY MALFORMATIONS, Clinical genetics, 54(4), 1998, pp. 330-333

Authors: BENZACKEN B LAPIERRE JM SIFFROI JP CHALVON A TACHDJIAN G
Citation: B. Benzacken et al., IDENTIFICATION AND CHARACTERIZATION OF A DE-NOVO PARTIAL TRISOMY 10P BY COMPARATIVE GENOMIC HYBRIDIZATION (CGH), Clinical genetics, 54(4), 1998, pp. 334-340

Authors: JENDERNY J SCHMIDT W HELD KR
Citation: J. Jenderny et al., PRESENCE OF THE AZF REGION IN A FEMALE WITH AN IDIC(Y)(Q11), Clinical genetics, 54(4), 1998, pp. 341-344
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