List of bibliographic references
Number of relevant bibliographic references: 40.
[0-20] [
0 - 20][
0 - 40][
20-40]
| Ident. | Authors (with country if any) | Title |
|---|
| 000700 (2011) |
Liran Horev [Israël] ; Melissa M. Lees [Royaume-Uni] ; Irene Anteby [Israël] ; John M. Gomori [Israël] ; Roxana Gunny [Royaume-Uni] ; Ziva Ben-Neriah [Israël] | Oculoectodermal syndrome with coarctation of the aorta and moyamoya disease: Expanding the phenotype to include vascular anomalies |
| 000B71 (2010) |
| A ‐ Dysmorphology and Multiple Anomalies |
| 000D94 (2009) |
Maria Leine Guion-Almeida [Brésil] ; Antonio Richieri-Costa [Brésil] | Frontonasal dysplasia, severe neuropsychological delay, and midline central nervous system anomalies: Report of 10 Brazilian male patients |
| 001087 (2008) |
Mireile N. Bekker [Pays-Bas] ; Nynke M. S. Van Den Akker [Pays-Bas] ; Yolanda M. De Mooij [Pays-Bas] ; Margot M. Bartelings [Pays-Bas] ; John M. G. Van Vugt [Pays-Bas] ; Adriana C. Gittenberger-De Groot [Pays-Bas] | Jugular Lymphatic Maldevelopment in Turner Syndrome and Trisomy 21: Different Anomalies Leading to Nuchal Edema |
| 001254 (2007) |
Miikka Vikkula [Belgique] | Vascular anomalies |
| 001451 (2007) |
Jiri Sonek [États-Unis] | First trimester ultrasonography in screening and detection of fetal anomalies |
| 002256 (2003) |
Roopal V. Kundu ; Ilona J. Frieden [États-Unis] | Presence of Vascular Anomalies with Congenital Hemihypertrophy and Wilms Tumor: An Evidence‐Based Evaluation |
| 002583 (2002) |
Edmond G. Lemire [Canada] | Noonan syndrome or new autosomal dominant condition with coarctation of the aorta, hypertrophic cardiomyopathy, and minor anomalies |
| 002F26 (2000) |
John B. Mulliken [États-Unis] ; Steven J. Fishman [États-Unis] ; Patricia E. Burrows [États-Unis] | Vascular anomalies |
| 002F94 (2000) |
Peter Michael Kroisel [Autriche] ; Erwin Petek [Autriche] ; Klaus Wagner [Autriche] | Skin pigmentary anomalies in a mosaic form of partial tetrasomy 3q |
| 003198 (2000) |
John M. Opitz [États-Unis] | Heterogeneity and minor anomalies |
| 003199 (2000) |
John M. Opitz [États-Unis] | Heterogeneity and minor anomalies |
| 003640 (1999) |
Anne M. Hubbard [États-Unis] ; Patricia Harty [États-Unis] | Prenatal magnetic resonance imaging of fetal anomalies |
| 003F07 (1997) |
M. S. Williams [États-Unis] ; K. D. Josephson [États-Unis] | Unusual autosomal recessive lymphatic anomalies in two unrelated Amish families |
| 004074 (1997) |
Luis Requena ; Omar P. Sangueza | Cutaneous vascular anomalies. Part I. Hamartomas, malformations, and dilatation of preexisting vessels |
| 004352 (1996) |
Axel Bohring [Allemagne] ; Josef Sonntag [Allemagne] ; Heinz Schröder [Allemagne] ; Hans-Rudolf Wiedemann [Allemagne] | Unusual complex of ventral midline anomalies: A multiple congenital anomalies/mental retardation syndrome |
| 004525 (1996) |
Tomonobu Hasegawa [Japon] ; Tsutomu Ogata [Japon] ; Yukihiro Hasegawa [Japon] ; Masataka Honda [Japon] ; Toshiro Nagai [Japon] ; Yoshimitsu Fukushima [Japon] ; Yutaka Nakahori [Japon] ; Nobutake Matsuo [Japon] | Coarctation of the aorta and renal hypoplasia in a boy with Turner/Noonan surface anomalies and a 46,XY karyotype: A clinical model for the possible impairment of a putative lymphogenic gene(s) for Turner somatic stigmata |
| 004E06 (1993) |
M. Urioste [Espagne] ; José I. Rodríguez [Espagne] ; José M. Barcia [Espagne] ; Martín Martín [Espagne] ; Rosa Escribá [Espagne] ; Marina Pardo [Espagne] ; J. Camino [Espagne] ; María Luisá Martínez- Frías [Espagne] | Persistence of müllerian derivatives, lymphangiectasis, hepatic failure, postaxial polydactyly, renal and craniofacial anomalies |
| 004E40 (1993) |
M. E. Spearritt [Australie] ; A. E. G. Tannenberg [Australie] ; D. J. Payton [Australie] | Lethal multiple pterygium syndrome: Report of a case with neurological anomalies |
| 005086 (1992) |
A. Richieri-Costa [Brésil] ; M. L. Guion-Almeida [Brésil] ; A. L. Ramos [Brésil] | New syndrome: Mental retardation, microbrachycephaly, hypotelorism, palpebral ptosis, thin/long face, cleft lip, and lumbosacral/pelvic anomalies |
| 005087 (1992) |
Zvi Borochowitz [Israël] ; Lorenzo Pavone [Italie] ; Galia Mazor [Israël] ; Renata Rizzo [Italie] ; Hanna Dar [Israël] | New multiple congenital anomalies: Mental retardation syndrome (MCA/MR) with facio‐cutaneous‐skeletal involvement |
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