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...

Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease

Nature genetics, 1992-09, Vol.2 (1), p.37-41

1992

Volltextzugriff (PDF)

Mapping of a gene determining tuberous sclerosis to human chromosome 11q1411q23

Genomics (San Diego, Calif.), 1990, Vol.6 (1), p.105-114

1990

Volltextzugriff (PDF)

A single base mutation that converts glycine 907 of the alpha 2(I) chain of type I procollagen to aspartate in a lethal variant of osteogenesis imperfecta. The single amino acid substitution near the carboxyl terminus destabilizes the whole triple helix

The Journal of biological chemistry, 1989-02, Vol.264 (5), p.3002-3006

1989

Volltextzugriff (PDF)

A single base mutation that converts glycine 907 of the α2(I) chain of type I procollagen to aspartate in a lethal variant of osteogenesis imperfecta: the single amino acid substitution near the carboxyl terminus destabilizes the whole triple helix

The Journal of biological chemistry, 1989, Vol.264 (5), p.3002-3006

1989

Volltextzugriff (PDF)

Genetic associate training program

Academic medicine, 1978-09, Vol.53 (9), p.768-70

Dumars, K W

1978

Volltextzugriff (PDF)

Parental drug usage: effect upon chromosomes of progeny

Pediatrics (Evanston), 1971-06, Vol.47 (6), p.1037-1041

Dumars, Jr, K W

1971

Volltextzugriff (PDF)

The Adopted Child and Congenital Malformations

Clinical pediatrics, 1967-12, Vol.6 (12), p.696-698

Dumars, K.W.

1967

Volltextzugriff (PDF)

Prevention of developmental disabilities: A model for organizing clinical activities

Research in developmental disabilities, 1987, Vol.8 (4), p.507-520

1987

Volltextzugriff (PDF)

Screening for developmental disabilities

The Western journal of medicine, 1985-09, Vol.143 (3), p.349

1985

Volltextzugriff (PDF)

Amniotic-fluid-cell-culture failure and syringe toxicity revisited

American journal of human genetics, 1982-09, Vol.34 (5), p.823-826

1982

Volltextzugriff (PDF)

Cancer, chromosomes and congenital abnormalities

Cancer, 1967-06, Vol.20 (6), p.1006-1014

1967

Volltextzugriff (PDF)

Cutis aplasia and cerebral malformation

Pediatrics (Evanston), 1973-12, Vol.52 (6), p.861-864

1973

Volltextzugriff (PDF)

Antiviral Activities of Amniotic Fluid

Experimental biology and medicine (Maywood, N.J.), 1981-12, Vol.168 (3), p.403-407

1981

Volltextzugriff (PDF)

Association of terminal chromosome 1 deletion with Sertoli cell-only syndrome

American journal of medical genetics, 1998-12, Vol.80 (4), p.396-398

1998

Volltextzugriff (PDF)

LE CRI DU CHAT (CRYING CAT) SYNDROME

American journal of diseases of children (1960), 1964-11, Vol.108 (5), p.533

1964

Volltextzugriff (PDF)

Roentgenographic features of the cerebrohepatorenal syndrome of Zellweger

American journal of roentgenology (1976), 1972-07, Vol.115 (3), p.607-610

1972

Volltextzugriff (PDF)

Midline defects of the back: Pediatric view

GP, 1969-10, Vol.40 (4), p.132

Dumars, Jr, K W

1969

Volltextzugriff (PDF)

Prenatal diagnosis of chromosomal and enzymatic defects

Obstetrics and gynecology (New York. 1953), 1976-04, Vol.47 (4), p.503

1976

Volltextzugriff (PDF)

Variation in pituitary-gonadal function in adolescent male homosexuals and heterosexuals

The journal of clinical endocrinology and metabolism, 1974-10, Vol.39 (4), p.796-801

1974

Volltextzugriff (PDF)

Fetal sex determination

Acta cytologica, 1973-05, Vol.17 (3), p.233

1973

Volltextzugriff (PDF)

INCOMPLETE EXSTROPHY OF THE CLOACA

The Journal of urology, 1964-05, Vol.91 (5), p.549-552

1964

Volltextzugriff (PDF)

Prenatal diagnosis and genetic counseling

The Western journal of medicine, 1976-05, Vol.124 (5), p.377

1976

Volltextzugriff (PDF)

Minimizing the risk of amniocentesis for prenatal diagnosis

JAMA : the journal of the American Medical Association, 1977-03, Vol.237 (13), p.1336

1977

Volltextzugriff (PDF)

Oculo-auriculo-vertebral dysplasia--Goldenhar's syndrome

Rocky Mountain medical journal, 1968-04, Vol.65 (4), p.44

1968

Volltextzugriff (PDF)

Familial t(4;13) with abnormal offspring in three generations

American journal of medical genetics, 1983-09, Vol.16 (1), p.15-22

1983

Volltextzugriff (PDF)

1 – 25 von 60

Menü

Weitere Dienste

Einstellungen

Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease

Mapping of a gene determining tuberous sclerosis to human chromosome 11q1411q23

A single base mutation that converts glycine 907 of the alpha 2(I) chain of type I procollagen to aspartate in a lethal variant of osteogenesis imperfecta. The single amino acid substitution near the carboxyl terminus destabilizes the whole triple helix

A single base mutation that converts glycine 907 of the α2(I) chain of type I procollagen to aspartate in a lethal variant of osteogenesis imperfecta: the single amino acid substitution near the carboxyl terminus destabilizes the whole triple helix

Genetic associate training program

Parental drug usage: effect upon chromosomes of progeny

The Adopted Child and Congenital Malformations

Prevention of developmental disabilities: A model for organizing clinical activities

Screening for developmental disabilities

Amniotic-fluid-cell-culture failure and syringe toxicity revisited

Cancer, chromosomes and congenital abnormalities

Cutis aplasia and cerebral malformation

Antiviral Activities of Amniotic Fluid

Association of terminal chromosome 1 deletion with Sertoli cell-only syndrome

LE CRI DU CHAT (CRYING CAT) SYNDROME

Roentgenographic features of the cerebrohepatorenal syndrome of Zellweger

Midline defects of the back: Pediatric view

Prenatal diagnosis of chromosomal and enzymatic defects

Variation in pituitary-gonadal function in adolescent male homosexuals and heterosexuals

Fetal sex determination

INCOMPLETE EXSTROPHY OF THE CLOACA

Prenatal diagnosis and genetic counseling

Minimizing the risk of amniocentesis for prenatal diagnosis

Oculo-auriculo-vertebral dysplasia--Goldenhar's syndrome

Familial t(4;13) with abnormal offspring in three generations

Suchergebnisse filtern