Search research articles
Contact Us
Filters
Showing results (21-30 of 177) with videos related to
Page
of 18
Sort By:
American Journal of Medical Genetics
|
August 15, 1994
Intermittent hair loss in a child with PIBI(D)S syndrome and trichothiodystrophy with defective DNA repair-xeroderma pigmentosum group D
W J Kleijer, F A Beemer, B W Boom
European Journal of Pediatrics
|
December 1, 1986
The velo-cardio-facial (Shprintzen) syndrome. Clinical variability in eight patients
P Meinecke, F A Beemer, A Schinzel, et al.
Lancet (London, England)
|
March 21, 1981
Early diagnosis of skeletal dysplasia by real-time ultrasound
J W Wladimiroff, F A Beemer, A M Hemmes
Clinical Dysmorphology
|
January 1, 1994
DOOR syndrome: additional case and literature review
C J Bos, P F Ippel, F A Beemer
American Journal of Medical Genetics
|
January 1, 1986
Cerebral gigantism (Sotos syndrome) in two patients with fra(X) chromosomes
F A Beemer, H Veenema, J M de Pater
Clinical Dysmorphology
|
April 18, 1998
Unusual association of congenital malformations: craniosynostosis, heart defect, abnormal intestinal innervation and urogenital abnormalities
B P Van Nesselrooij, W Spliet, F A Beemer
Nederlands Tijdschrift Voor Geneeskunde
|
May 28, 1994
[An unusual cause of hypertension during pregnancy with fatal outcome]
G J Brouwers-Smalbraak, F A Beemer, C J Lips
Clinical Genetics
|
October 1, 1984
Duplication in chromosome 15q in a boy with the Prader-Willi syndrome; further cytogenetic confusion
H F de France, F A Beemer, P F Ippel
Nature
|
August 5, 1984
How did retinoblastoma arise?
F A Beemer, C W Van Veelen, G E Staal
Nederlands Tijdschrift Voor Geneeskunde
|
September 22, 1984
[Abnormal transaminase values in children: consider the muscles]
T W Schulpen, F A Beemer, C van der Heiden
Page
of 18
Search research articles
Search
Showing results (21-30 of 177) with videos related to
Sort By:
Page
of 18
American Journal of Medical Genetics
|
August 15, 1994
Intermittent hair loss in a child with PIBI(D)S syndrome and trichothiodystrophy with defective DNA repair-xeroderma pigmentosum group D
W J Kleijer, F A Beemer, B W Boom
European Journal of Pediatrics
|
December 1, 1986
The velo-cardio-facial (Shprintzen) syndrome. Clinical variability in eight patients
P Meinecke, F A Beemer, A Schinzel, et al.
Lancet (London, England)
|
March 21, 1981
Early diagnosis of skeletal dysplasia by real-time ultrasound
J W Wladimiroff, F A Beemer, A M Hemmes
Clinical Dysmorphology
|
January 1, 1994
DOOR syndrome: additional case and literature review
C J Bos, P F Ippel, F A Beemer
American Journal of Medical Genetics
|
January 1, 1986
Cerebral gigantism (Sotos syndrome) in two patients with fra(X) chromosomes
F A Beemer, H Veenema, J M de Pater
Clinical Dysmorphology
|
April 18, 1998
Unusual association of congenital malformations: craniosynostosis, heart defect, abnormal intestinal innervation and urogenital abnormalities
B P Van Nesselrooij, W Spliet, F A Beemer
Nederlands Tijdschrift Voor Geneeskunde
|
May 28, 1994
[An unusual cause of hypertension during pregnancy with fatal outcome]
G J Brouwers-Smalbraak, F A Beemer, C J Lips
Clinical Genetics
|
October 1, 1984
Duplication in chromosome 15q in a boy with the Prader-Willi syndrome; further cytogenetic confusion
H F de France, F A Beemer, P F Ippel
Nature
|
August 5, 1984
How did retinoblastoma arise?
F A Beemer, C W Van Veelen, G E Staal
Nederlands Tijdschrift Voor Geneeskunde
|
September 22, 1984
[Abnormal transaminase values in children: consider the muscles]
T W Schulpen, F A Beemer, C van der Heiden
Page
of 18