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American Journal of Medical Genetics
|
October 1, 1990
Agnathia, holoprosencephaly, and situs inversus: a third report
P Meinecke, B Padberg, R Laas
Klinische Padiatrie
|
January 1, 1983
[Congenital contractural arachnodactyly (CCA syndrome)--an autosomal dominant hereditary connective tissue disease]
P Meinecke, E Schaefer, E Passarge
Clinical Dysmorphology
|
July 1, 1992
Setleis (bitemporal 'forceps marks') syndrome in a German family: evidence for autosomal dominant inheritance
A Artlich, E Schwinger, P Meinecke
Genetic Counseling (Geneva, Switzerland)
|
February 1, 2003
Defective clavicles in Kabuki syndrome
B Hinrichs, B Gramss, P Meinecke
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
February 1, 1990
[Brachmann-de Lange syndrome in 16 of our patients]
R Pankau, W Johannson, P Meinecke
Clinical Dysmorphology
|
January 1, 1992
Microgastria-hypoplastic upper limb association: a severe expression including microphthalmia, single nostril and arhinencephaly
P Meinecke, C G Bönnemann, R Laas
American Journal of Medical Genetics
|
May 1, 1991
Microcephalic osteodysplastic primordial dwarfism: further evidence for identity of the so-called types I and III
P Meinecke, E Schaefer, H R Wiedemann
Journal of Medical Genetics
|
January 1, 1991
Balanced t(6;8)(6p8p;6q8q) and the CHARGE association
J A Hurst, P Meinecke, M Baraitser
Journal of Medical Genetics
|
October 1, 1991
Encephalopathy with intracerebral calcification, white matter lesions, growth hormone deficiency, microcephaly, and retinal degeneration: two sibs confirming a probably distinct entity
C G Bönnemann, P Meinecke, H Reich
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
April 1, 1989
[Knee pterygium syndrome in a newborn infant]
P Meinecke, J Menzel, U Froster-Iskenius
Page
of 10
Search research articles
Search
Showing results (41-50 of 93) with videos related to
Sort By:
Page
of 10
American Journal of Medical Genetics
|
October 1, 1990
Agnathia, holoprosencephaly, and situs inversus: a third report
P Meinecke, B Padberg, R Laas
Klinische Padiatrie
|
January 1, 1983
[Congenital contractural arachnodactyly (CCA syndrome)--an autosomal dominant hereditary connective tissue disease]
P Meinecke, E Schaefer, E Passarge
Clinical Dysmorphology
|
July 1, 1992
Setleis (bitemporal 'forceps marks') syndrome in a German family: evidence for autosomal dominant inheritance
A Artlich, E Schwinger, P Meinecke
Genetic Counseling (Geneva, Switzerland)
|
February 1, 2003
Defective clavicles in Kabuki syndrome
B Hinrichs, B Gramss, P Meinecke
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
February 1, 1990
[Brachmann-de Lange syndrome in 16 of our patients]
R Pankau, W Johannson, P Meinecke
Clinical Dysmorphology
|
January 1, 1992
Microgastria-hypoplastic upper limb association: a severe expression including microphthalmia, single nostril and arhinencephaly
P Meinecke, C G Bönnemann, R Laas
American Journal of Medical Genetics
|
May 1, 1991
Microcephalic osteodysplastic primordial dwarfism: further evidence for identity of the so-called types I and III
P Meinecke, E Schaefer, H R Wiedemann
Journal of Medical Genetics
|
January 1, 1991
Balanced t(6;8)(6p8p;6q8q) and the CHARGE association
J A Hurst, P Meinecke, M Baraitser
Journal of Medical Genetics
|
October 1, 1991
Encephalopathy with intracerebral calcification, white matter lesions, growth hormone deficiency, microcephaly, and retinal degeneration: two sibs confirming a probably distinct entity
C G Bönnemann, P Meinecke, H Reich
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
April 1, 1989
[Knee pterygium syndrome in a newborn infant]
P Meinecke, J Menzel, U Froster-Iskenius
Page
of 10