UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Isolation of a candidate gene for Norrie disease by positional cloning

Nature genetics, 1992-06, Vol.1 (3), p.199-203

1992

Volltextzugriff (PDF)

The future of human genetics is the faster continuum of the past

Acta medica Croatica, 1999, Vol.53 (2), p.55

Zergollern, L

1999

Volltextzugriff (PDF)

Development of genetics in the world and in Croatia--forty years of the Croatian Society of Human Genetics of the Croatian Medical Association

Collegium antropologicum, 2014-09, Vol.38 (3), p.809-818

2014

Volltextzugriff (PDF)

Three generations and seven family members with a t(21q22q) chromosome

Journal of medical genetics, 1974-12, Vol.11 (4), p.379-381

Zergollern, L

1974

Volltextzugriff (PDF)

The genetics of polycystic ovaries

Liječnički vjesnik, 1996-03, Vol.118 Suppl 1, p.17

Zergollern, L

1996

Volltextzugriff (PDF)

Four siblings with Robert's syndrome

Clinical genetics, 1982-01, Vol.21 (1), p.1-6

1982

Volltextzugriff (PDF)

A follow-up on Hanhart's dwarfs of Krk

Birth defects original article series, 1971-05, Vol.7 (6), p.28

Zergollern, L

1971

Volltextzugriff (PDF)

Megalocornea-mental retardation syndrome: report of a new case

Journal of medical genetics, 1996-10, Vol.33 (10), p.882-883

1996

Volltextzugriff (PDF)

Human genetics and ethics

Liječnički vjesnik, 1990-01, Vol.112 (1-2), p.63

Zergollern, L

1990

Volltextzugriff (PDF)

An unusual hand and foot malformation (author's transl)

Liječnički vjesnik, 1976, Vol.98 (10), p.531

1976

Volltextzugriff (PDF)

Duplication 15q22 to 15qter and its phenotypic expression

Human genetics, 1981, Vol.59 (4), p.429-433

1981

Volltextzugriff (PDF)

Risk estimates for balanced reciprocal translocation carriers - prenatal diagnosis experience

Clinical genetics, 1996-03, Vol.49 (3), p.145-151

1996

Volltextzugriff (PDF)

Norrie-Warburg syndrome

Acta medica Iugoslavica, 1986, Vol.40 (4), p.263

1986

Volltextzugriff (PDF)

De novo terminal deletion del(3) (p25 leads to pter)

Acta medica Iugoslavica, 1983, Vol.37 (3), p.263

1983

Volltextzugriff (PDF)

First results in prenatal diagnosis

Acta medica Iugoslavica, 1982, Vol.36 (1), p.3

1982

Volltextzugriff (PDF)

Cytogenetics of spontaneous abortions

Acta medica Iugoslavica, 1982, Vol.36 (2), p.107

1982

Volltextzugriff (PDF)

Partial trisomy 22

Acta medica Iugoslavica, 1979-12, Vol.33 (5), p.459

1979

Volltextzugriff (PDF)

49,xxxxy syndrome associated with congenital heart disease (author's transl)

Liječnički vjesnik, 1976-07, Vol.98 (7), p.366

1976

Volltextzugriff (PDF)

Ring chromosome 21

Acta medica Iugoslavica, 1989, Vol.43 (2), p.147

1989

Volltextzugriff (PDF)

Focal dermal hypoplasia

Dermatologica, 1974-01, Vol.148 (4), p.240-246

1974

Volltextzugriff (PDF)

Diaphragmatic hernias as an associated symptom of chromosomopathies (author's transl)

Liječnički vjesnik, 1979-01, Vol.101 (1), p.18

1979

Volltextzugriff (PDF)

Medical genetics in pediatrics (author's transl)

Liječnički vjesnik, 1979-12, Vol.101 (12), p.743

Zergollern, L

1979

Volltextzugriff (PDF)

Cytomegalic Inclusion Disease: Report of a Case Diagnosed Radiologically

Acta radiologica (1987), 1972-01, Vol.13 (P1), p.3-7

1972

Volltextzugriff (PDF)

Fetal alcohol syndrome (embryopathia alcoholica)

Acta medica Iugoslavica, 1984, Vol.38 (5), p.355

1984

Volltextzugriff (PDF)

The Goltz-Gorlin syndrome in a male child

Liječnički vjesnik, 1989-03, Vol.111 (3), p.85

1989

Volltextzugriff (PDF)

1 – 25 von 94

Menü

Weitere Dienste

Einstellungen

Isolation of a candidate gene for Norrie disease by positional cloning

The future of human genetics is the faster continuum of the past

Development of genetics in the world and in Croatia--forty years of the Croatian Society of Human Genetics of the Croatian Medical Association

Three generations and seven family members with a t(21q22q) chromosome

The genetics of polycystic ovaries

Four siblings with Robert's syndrome

A follow-up on Hanhart's dwarfs of Krk

Megalocornea-mental retardation syndrome: report of a new case

Human genetics and ethics

An unusual hand and foot malformation (author's transl)

Duplication 15q22 to 15qter and its phenotypic expression

Risk estimates for balanced reciprocal translocation carriers - prenatal diagnosis experience

Norrie-Warburg syndrome

De novo terminal deletion del(3) (p25 leads to pter)

First results in prenatal diagnosis

Cytogenetics of spontaneous abortions

Partial trisomy 22

49,xxxxy syndrome associated with congenital heart disease (author's transl)

Ring chromosome 21

Focal dermal hypoplasia

Diaphragmatic hernias as an associated symptom of chromosomopathies (author's transl)

Medical genetics in pediatrics (author's transl)

Cytomegalic Inclusion Disease: Report of a Case Diagnosed Radiologically

Fetal alcohol syndrome (embryopathia alcoholica)

The Goltz-Gorlin syndrome in a male child

Suchergebnisse filtern