PREVALENCE OF EDWARDS' SYNDROME. CLUSTERING AND SEASONAL VARIATION. = FREQUENCE DU SYNDROME D'EDWARDS. FOCALISATION ET VARIATION SAISONNIERE.NIELSEN J; HOLM V; HAAHR J et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 26; NO 2; PP. 113-116; BIBL. 8REF.Article

INVERSION 19 AND ISOCHROMOSOME SHORT ARM 17 OR 18.NIELSEN J; HOMMA A; HOLM V et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 37; NO 3; PP. 347-350; BIBL. 6 REF.Article

RELATIVE BIOAVAILABILITY OF PHENOXYMETHYLPENICILLIN PREPARATIONS IN A CROSS-OVER STUDYBERGAN T; BERDAL BP; HOLM V et al.1976; ACTA PHARMACOL. TOXICOL.; DANEM.; DA. 1976; VOL. 38; NO 4; PP. 308-320; BIBL. 18 REF.Article

ABSORPTION STUDY OF NITRAZEPAM TABLETS (APODORM)BJELLAND L; GJERMUNDSEN R; HOLM V et al.1974; MEDD. NORSK FARM. SELSK.; NORGE; DA. 1974; VOL. 36; NO 3; PP. 129-142; BIBL. 13REF.Article

RELATIVE BIOAVAILABILITY OF METHAQUALONE FROM TABLETS, ALONE AND IN COMBINATION WITH DIPHENHYDRAMINE.FREDERICHSEN P; WAALER T; GJERMUNDSEN R et al.1977; MEDD. NORSK. FARM. SELSK.; NORGE; DA. 1977; VOL. 39; NO 2; PP. 99-109; BIBL. 9 REF.Article

BOERN MED KROMOSOMABNORMITETER I EN PAEDIATRISK AFDELING = LES ENFANTS PORTEURS D'ANOMALIES CHROMOSOMIQUES DANS UN DEPARTEMENT DE PEDIATRIENIELSEN J; FRIEDRICH U; HOLM V et al.1973; UGESKR. LAEGER; DANM.; DA. 1973; VOL. 135; NO 8; PP. 408-415; ABS. ANGL.; BIBL. 24 REF.Serial Issue

TURNER-FAENOTYPE HOS MAEND = PHENOTYPES DE TURNER CHEZ DES HOMMESNIELSEN J; FRIEDRICH U; HOLM V et al.1973; UGESKR. LAEGER; DANM.; DA. 1973; VOL. 135; NO 3; PP. 122-124; ABS. ANGL.; BIBL. 10 REF.Article

CHROMOSOME ABNORMALITIES IN CHILDREN, IN TWO DANISH COUNTIES, BORN DURING THE PERIOD 1967-1978. CLINICAL DATANIELSEN J; KRAG OLSEN B; DIRDAL M et al.1982; HEREDITAS; ISSN 0018-0661; SWE; DA. 1982; VOL. 96; NO 2; PP. 195-210; BIBL. 38 REF.Article

FRAGILE SITE LONG ARM CHROMOSOME 16S NONORESEN K; NIELSEN J; HOLM V et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 48; NO 1; PP. 131-134; BIBL. 10 REF.Article

CHROMOSOME VARIANTS IN CHILDREN REFERRED FOR CYTOGENETIC EXAMINATION FROM TWO PAEDIATRIC DEPARTMENTS DURING A 12-YEAR-PERIODKRAG OLSEN B; NIELSEN J; DIRDAL M et al.1980; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1980; VOL. 56; NO 1; PP. 67-69; BIBL. 15 REF.Article

Prader-Willi Syndrome Association. Annual scientific meetingHOLM, V. A.Dysmorphology and clinical genetics. 1992, Vol 6, Num 1, pp 22-33, issn 0893-6633Conference Proceedings

New directory, foreign and domestic growth, other news and notesDysmorphology and clinical genetics. 1992, Vol 6, Num 1, pp 44-46, issn 0893-6633Conference Paper

Advances in human molecular genetics influence clinical genetic practiceWARREN, S. T.Dysmorphology and clinical genetics. 1992, Vol 6, Num 1, pp 34-36, issn 0893-6633Conference Paper

New syndromes : updates to the Birth Defects EncyclopediaTORIELLO, H. V.Dysmorphology and clinical genetics. 1992, Vol 6, Num 1, pp 39-43, issn 0893-6633Conference Paper

A two-year follow-up of autistic children treated with fenfluramineVARLEY, C. K; HOLM, V. A.Journal of the American Academy of Child and Adolescent Psychiatry. 1990, Vol 29, Num 1, pp 137-140, issn 0890-8567Article

Quality changes in semi-hard cheese packaged in a poly(lactic acid) materialHOLM, V. K; MORTENSEN, G; RISBO, J et al.Food chemistry. 2006, Vol 97, Num 3, pp 401-410, issn 0308-8146, 10 p.Article

Deletion of chromosome 15(q11-13) in a Prader-Labhart-Willi syndrome clinic populationCASSIDY, S. B; THULINE, H. C; HOLM, V. A et al.American journal of medical genetics. 1984, Vol 17, Num 2, pp 485-495, issn 0148-7299Article

Infant walkers and cerebral palsyHOLM, V. A; HARTHUN-SMITH, L; TADA, W. L et al.American journal of diseases of children (1960). 1983, Vol 137, Num 12, pp 1189-1190, issn 0002-922XArticle

Annual Scientific Conference of the Prader-Willi Syndrome Association (USA)HOLM, V. A; HUDGINS, L; CASSIDY, S. B et al.American journal of medical genetics. 1996, Vol 64, Num 4, pp 573-579, issn 0148-7299Conference Proceedings

Oxandrolone therapy in six boys with the Prader-Willi syndromeHOLM, V. A; NUGENT, J. K; RUVALCABA, R. H. A et al.The Journal of pediatrics. 1989, Vol 114, Num 2, pp 325-327, issn 0022-3476Article

Aldolization of butyraldehyde with formaldehyde over a commercial anion-exchange resin: kinetics and selectivity aspectsSERRA-HOLM, V; SALMI, T; MULTAMÄKI, J et al.Applied catalysis. A, General. 2000, Vol 198, Num 1-2, pp 207-221, issn 0926-860XArticle

A new Rett syndrome family consistent with X-linked inheritance expands the X chromosome exclusion mapSCHANEN, N. C; DAHLE, E. J. R; CAPOZZOLI, F et al.American journal of human genetics. 1997, Vol 61, Num 3, pp 634-641, issn 0002-9297Article

Proximal trisomy 1q in a girl with developmental delay and minor anomaliesFURFORO, L; RITTLER, M; SLAVUTSKY, I. R et al.American journal of medical genetics. 1996, Vol 64, Num 4, pp 551-555, issn 0148-7299Conference Paper

Variant of Coffin-Siris syndrome or previously undescribed syndrome ?BRAUN-QUENTIN, C; KAPFERER, L; KOTZOT, D et al.American journal of medical genetics. 1996, Vol 64, Num 4, pp 568-572, issn 0148-7299Conference Paper

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