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
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
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
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
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:
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:
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