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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 30, 2001
Neurodevelopmental risks in twin-to-twin transfusion syndrome: preliminary findings
F Haverkamp, C Lex, C Hanisch, et al.
Klinische Padiatrie
|
July 21, 2005
[Achievement motivation in children with migraine and their healthy siblings]
F Haverkamp, A Hönscheid, M Rünger, et al.
Klinische Padiatrie
|
May 1, 1997
[Subacute sclerosing panencephalitis (SSPE) as differential diagnosis in severe personality changes and ataxia--case report and literature review]
J Wölfle, J Schmidt, B Kreft, et al.
Hormone Research
|
January 1, 1991
Constitutional delay of growth and puberty: do they really reach their target height?
G von Kalckreuth, F Haverkamp, M Kessler, et al.
Annales De Genetique
|
January 1, 1988
Hydrops fetalis as an indication for prenatal chromosome analysis with the example of the diagnosis of a duplication 15q11 and 17q25 due to a familial translocation 15/17
G Schwanitz, K Zerres, M Niesen, et al.
International Journal of Pediatric Otorhinolaryngology
|
January 1, 1996
Craniometaphyseal dysplasia as a rare cause of a severe neonatal nasal obstruction
F Haverkamp, D Emons, H J Straehler-Pohl, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
June 1, 1990
[Listeria meningoencephalitis in a 2-year-old boy]
G von Kalckreuth, D Staab, F Haverkamp, et al.
Journal of Medical Genetics
|
March 1, 1995
Familial schizencephaly: further delineation of a rare disorder
F Haverkamp, K Zerres, B Ostertun, et al.
Clinical Genetics
|
August 1, 1997
Partial trisomy 6p from a de novo translocation (6;18) with variable mosaicism in different tissues
S Rudnik-Schöneborn, R Schubert, F Majewski, et al.
American Journal of Medical Genetics
|
December 1, 1991
Syndrome of developmental retardation, facial and skeletal anomalies, and hyperphosphatasia in two sisters: nosology and genetics of the Coffin-Siris syndrome
P Rabe, F Haverkamp, D Emons, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 65) with videos related to
Sort By:
Page
of 7
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 30, 2001
Neurodevelopmental risks in twin-to-twin transfusion syndrome: preliminary findings
F Haverkamp, C Lex, C Hanisch, et al.
Klinische Padiatrie
|
July 21, 2005
[Achievement motivation in children with migraine and their healthy siblings]
F Haverkamp, A Hönscheid, M Rünger, et al.
Klinische Padiatrie
|
May 1, 1997
[Subacute sclerosing panencephalitis (SSPE) as differential diagnosis in severe personality changes and ataxia--case report and literature review]
J Wölfle, J Schmidt, B Kreft, et al.
Hormone Research
|
January 1, 1991
Constitutional delay of growth and puberty: do they really reach their target height?
G von Kalckreuth, F Haverkamp, M Kessler, et al.
Annales De Genetique
|
January 1, 1988
Hydrops fetalis as an indication for prenatal chromosome analysis with the example of the diagnosis of a duplication 15q11 and 17q25 due to a familial translocation 15/17
G Schwanitz, K Zerres, M Niesen, et al.
International Journal of Pediatric Otorhinolaryngology
|
January 1, 1996
Craniometaphyseal dysplasia as a rare cause of a severe neonatal nasal obstruction
F Haverkamp, D Emons, H J Straehler-Pohl, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
June 1, 1990
[Listeria meningoencephalitis in a 2-year-old boy]
G von Kalckreuth, D Staab, F Haverkamp, et al.
Journal of Medical Genetics
|
March 1, 1995
Familial schizencephaly: further delineation of a rare disorder
F Haverkamp, K Zerres, B Ostertun, et al.
Clinical Genetics
|
August 1, 1997
Partial trisomy 6p from a de novo translocation (6;18) with variable mosaicism in different tissues
S Rudnik-Schöneborn, R Schubert, F Majewski, et al.
American Journal of Medical Genetics
|
December 1, 1991
Syndrome of developmental retardation, facial and skeletal anomalies, and hyperphosphatasia in two sisters: nosology and genetics of the Coffin-Siris syndrome
P Rabe, F Haverkamp, D Emons, et al.
Page
of 7