UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 47

Sortiert nach

Co-occurrence of Joubert syndrome and Jeune asphyxiating thoracic dystrophy

American journal of medical genetics. Part A, 2010-06, Vol.152A (6), p.1411-1419

2010

Volltextzugriff (PDF)

FOXL2 copy number changes in the molecular pathogenesis of BPES: unique cohort of 17 deletions

Human mutation, 2010-05, Vol.31 (5), p.E1332-E1347

2010

Volltextzugriff (PDF)

An update on the frequency of mucopolysaccharide syndromes in British Columbia

Human genetics, 1990-08, Vol.85 (3), p.389-390

1990

Volltextzugriff (PDF)

Interstitial Deletions at 6q14.1q15 Associated with Developmental Delay and a Marfanoid Phenotype

Molecular syndromology, 2013-09, Vol.4 (6), p.280-284

2013

Volltextzugriff (PDF)

Father-to-son transmission of an X-linked gene: A case of paternal sex chromosome heterodisomy

American journal of medical genetics. Part A, 2009-12, Vol.149A (12), p.2871-2873

2009

Volltextzugriff (PDF)

Bowen–Conradi syndrome: A clinical and genetic study

American journal of medical genetics, 2003-07, Vol.120A (3), p.423-428

2003

Volltextzugriff (PDF)

Association between congenital foot anomalies and gestational age at amniocentesis

Prenatal diagnosis, 2001-12, Vol.21 (13), p.1137-1141

2001

Volltextzugriff (PDF)

Cataracts, microcephaly, kyphosis, and limited joint movement in two siblings: A new syndrome

The Journal of pediatrics, 1971-08, Vol.79 (2), p.282-284

1971

Volltextzugriff (PDF)

Errors of morphogenesis: Concepts and terms

The Journal of pediatrics, 1982, Vol.100 (1), p.160-165

1982

Volltextzugriff (PDF)

Epidemiologic and morphologic studies of congenital anomalies and syndromes

Lowry, R.B

1989

Volltextzugriff (PDF)

A surface enhanced Raman spectroscopic study of electrode/electrolyte interface

Lowry, R.B

1988

Volltextzugriff (PDF)

Autosomal recessive, fatal infantile hypertonic muscular dystrophy among Canadian Natives

Canadian journal of neurological sciences, 1994-08, Vol.21 (3), p.203

1994

Volltextzugriff (PDF)

Reply

The Journal of pediatrics, 1973-02, Vol.82 (2), p.351-352

1973

Volltextzugriff (PDF)

Klippel-Trenaunay and Sturge-Weber syndrome with extensive Mongolian spots, hypoplastic larynx and subglottic stenosis

Clinical and experimental dermatology, 1988-03, Vol.13 (2), p.128-132

1988

Volltextzugriff (PDF)

LEGG-PERTHES' DISEASE AND GENITOURINARY-TRACT ANOMALIES

The Lancet (British edition), 1971-07, Vol.298 (7718), p.266-266

Lowry, R.B.

1971

Volltextzugriff (PDF)

RECURRENCE RISKS FOR CLEFT LIP AND CLEFT PALATE IN BRITISH COLUMBIA INDIANS

The Lancet (British edition), 1970-10, Vol.296 (7675), p.727-727

Lowry, R.B.

1970

Volltextzugriff (PDF)

Fourier transform SERS studies of the chemisorption of ferricyanide on gold electrode surfaces

Spectrochimica acta. Part A: Molecular spectroscopy, 1993-05, Vol.49 (5), p.831-836

Lowry, R.B.

1993

Volltextzugriff (PDF)

CLASSIFICATION AND NOMENCLATURE OF MALFORMATIONS

The Lancet (British edition), 1974-09, Vol.304 (7882), p.719-719

Lowry, R.B

1974

Volltextzugriff (PDF)

Characterization of an interstitial deletion del(13)(q22q32) using microdissection and sequential FISH and G-banding

Genetic testing, 2000, Vol.4 (3), p.279-282

2000

Volltextzugriff (PDF)

Tertiary trisomy (22q11q),47,+der(22),t(11;22)

Human genetics, 1980-02, Vol.53 (2), p.173-177

1980

Volltextzugriff (PDF)

INHERITANCE OF TUBEROUS SCLEROSIS

The Lancet (British edition), 1979-01, Vol.313 (8109), p.216-216

1979

Volltextzugriff (PDF)

Absent vagina and the Klippel-Feil anomaly

American journal of obstetrics and gynecology, 1974-01, Vol.118 (2), p.290-291

1974

Volltextzugriff (PDF)

The use of spontaneous abortuses and stillbirths in genetic counseling

American journal of obstetrics and gynecology, 1974-02, Vol.118 (3), p.322-326

1974

Volltextzugriff (PDF)

An electrochemical and SERS investigation of the influence of pH on the effectiveness of some corrosion inhibitors of copper

Journal of electroanalytical chemistry and interfacial electrochemistry, 1987-01, Vol.217 (1), p.187-202

1987

Volltextzugriff (PDF)

CLEFT PALATE AND CONGENITAL HEART-DISEASE

The Lancet (British edition), 1971-06, Vol.297 (7712), p.1302-1303

1971

Volltextzugriff (PDF)

1 – 25 von 47

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(37)
Mit Volltextzugriff
(40)

Publikationsform

Sprache

Englisch
(47)
Japanisch
(5)

Erscheinungsjahr

n.n

Thema

Science & Technology
(30)
Life Sciences & Biomedicine
(22)
Humans
(20)
Female
(14)
Male
(12)
Genetics & Heredity
(9)
Biological And Medical Sciences
(8)
Child
(6)
Medical Sciences
(6)
Child, Preschool
(5)
Infant
(5)
Pedigree
(5)
Physical Sciences
(5)
Abnormalities, Multiple - Genetics
(3)
Adolescent
(3)
Adult
(3)
Agriculture
(3)
Agriculture, Dairy & Animal Science
(3)
Animals
(3)
Fundamental And Applied Biological Sciences. Psychology
(3)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Co-occurrence of Joubert syndrome and Jeune asphyxiating thoracic dystrophy

FOXL2 copy number changes in the molecular pathogenesis of BPES: unique cohort of 17 deletions

An update on the frequency of mucopolysaccharide syndromes in British Columbia

Interstitial Deletions at 6q14.1q15 Associated with Developmental Delay and a Marfanoid Phenotype

Father-to-son transmission of an X-linked gene: A case of paternal sex chromosome heterodisomy

Bowen–Conradi syndrome: A clinical and genetic study

Association between congenital foot anomalies and gestational age at amniocentesis

Cataracts, microcephaly, kyphosis, and limited joint movement in two siblings: A new syndrome

Errors of morphogenesis: Concepts and terms

Epidemiologic and morphologic studies of congenital anomalies and syndromes

A surface enhanced Raman spectroscopic study of electrode/electrolyte interface

Autosomal recessive, fatal infantile hypertonic muscular dystrophy among Canadian Natives

Reply

Klippel-Trenaunay and Sturge-Weber syndrome with extensive Mongolian spots, hypoplastic larynx and subglottic stenosis

LEGG-PERTHES' DISEASE AND GENITOURINARY-TRACT ANOMALIES

RECURRENCE RISKS FOR CLEFT LIP AND CLEFT PALATE IN BRITISH COLUMBIA INDIANS

Fourier transform SERS studies of the chemisorption of ferricyanide on gold electrode surfaces

CLASSIFICATION AND NOMENCLATURE OF MALFORMATIONS

Characterization of an interstitial deletion del(13)(q22q32) using microdissection and sequential FISH and G-banding

Tertiary trisomy (22q11q),47,+der(22),t(11;22)

INHERITANCE OF TUBEROUS SCLEROSIS

Absent vagina and the Klippel-Feil anomaly

The use of spontaneous abortuses and stillbirths in genetic counseling

An electrochemical and SERS investigation of the influence of pH on the effectiveness of some corrosion inhibitors of copper

CLEFT PALATE AND CONGENITAL HEART-DISEASE

Suchergebnisse filtern