[Neural tube defects]

Same author

Genetic services in Romania.

European journal of human genetics : EJHG·1997

Same author

Distal arthrogryposis with autosomal dominant inheritance and reduced penetrance in females: the Gordon syndrome.

Clinical genetics·1993

Same author

Distal deletion of the long arm of chromosome number 1 (q43-->qter) associated with severe mental retardation and a nonspecific dysmorphic syndrome.

Annales de genetique·1992

Same author

Madelung deformity as a pathognomonic feature of the onycho-osteodysplasia syndrome.

Genetic counseling (Geneva, Switzerland)·1992

Same author

A syndrome of mental retardation, short stature, craniofacial anomalies with palpebral ptosis and pulmonary stenosis in three siblings with normal parents. An example of autosomal recessive inheritance of the Noonan phenotype?

Genetic counseling (Geneva, Switzerland)·1992

Same author

[Bioethics in Romania. Science is a challenge, bioethics is a response].

Endocrinologie·1991

Same journal

Monoclonal antibodies for prophylactic and therapeutic use against viral infections.

Pediatria polska·2020

Same journal

[Advances in clinical diagnosis, laboratory diagnosis and therapy of infectious diseases in the period 1908-2008].

Pediatria polska·2020

Same journal

[Barriers in breast feeding: contraindications].

Pediatria polska·1996

Same journal

[Echinococcosis infection in three children].

Pediatria polska·1996

Same journal

[Newborn baby with extreme acidosis].

Pediatria polska·1996

Same journal

[Robin sequence].

Pediatria polska·1996

Related Experiment Videos

[Neural tube defects]

Related Concept Videos

Genetic services in Romania.

Distal arthrogryposis with autosomal dominant inheritance and reduced penetrance in females: the Gordon syndrome.

Distal deletion of the long arm of chromosome number 1 (q43-->qter) associated with severe mental retardation and a nonspecific dysmorphic syndrome.

Madelung deformity as a pathognomonic feature of the onycho-osteodysplasia syndrome.

A syndrome of mental retardation, short stature, craniofacial anomalies with palpebral ptosis and pulmonary stenosis in three siblings with normal parents. An example of autosomal recessive inheritance of the Noonan phenotype?

[Bioethics in Romania. Science is a challenge, bioethics is a response].

Monoclonal antibodies for prophylactic and therapeutic use against viral infections.

[Advances in clinical diagnosis, laboratory diagnosis and therapy of infectious diseases in the period 1908-2008].

[Barriers in breast feeding: contraindications].

[Echinococcosis infection in three children].

[Newborn baby with extreme acidosis].

[Robin sequence].

Related Experiment Videos

[Neural tube defects]

Related Concept Videos

Related Articles

Genetic services in Romania.

Distal arthrogryposis with autosomal dominant inheritance and reduced penetrance in females: the Gordon syndrome.

Distal deletion of the long arm of chromosome number 1 (q43-->qter) associated with severe mental retardation and a nonspecific dysmorphic syndrome.

Madelung deformity as a pathognomonic feature of the onycho-osteodysplasia syndrome.

A syndrome of mental retardation, short stature, craniofacial anomalies with palpebral ptosis and pulmonary stenosis in three siblings with normal parents. An example of autosomal recessive inheritance of the Noonan phenotype?

[Bioethics in Romania. Science is a challenge, bioethics is a response].

Monoclonal antibodies for prophylactic and therapeutic use against viral infections.

[Advances in clinical diagnosis, laboratory diagnosis and therapy of infectious diseases in the period 1908-2008].

[Barriers in breast feeding: contraindications].

[Echinococcosis infection in three children].

[Newborn baby with extreme acidosis].

[Robin sequence].