List of bibliographic references indexed by Abnormalities, Multiple
Number of relevant bibliographic references: 22.
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20-40]
| Ident. | Authors (with country if any) | Title |
|---|
| 004122 (2012) |
Natalia Pastora [Espagne] ; Jesus Peralta ; Irene Canal-Fontcuberta ; Anna Grabowska ; Jose S. Pulido ; Jose Abelairas ; Felix Armada ; Alfredo Garcia-Alix | Microcephaly-lymphedema-chorioretinal dysplasia associated with pachymicrogyria and atrophy of the cerebellar vermis: an integration of brain-ocular migration disorders. |
| 005651 (2010) |
Alexander Kreuter ; Tim Waterboer ; Ulrike Wieland | Regression of cutaneous warts in a patient with WILD syndrome following recombinant quadrivalent human papillomavirus vaccination. |
| 005D27 (2010) |
Sahar Mansour [Royaume-Uni] ; Fiona Connell [Royaume-Uni] ; Colin Steward [Royaume-Uni] ; Pia Ostergaard [Royaume-Uni] ; Glen Brice [Royaume-Uni] ; Sarah Smithson [Royaume-Uni] ; Peter Lunt [Royaume-Uni] ; Steve Jeffery [Royaume-Uni] ; Inderjeet Dokal [Royaume-Uni] ; Tom Vulliamy [Royaume-Uni] ; Brenda Gibson [Royaume-Uni] ; Shirley Hodgson [Royaume-Uni] ; Sally Cottrell [Royaume-Uni] ; Louise Kiely [Royaume-Uni] ; Lorna Tinworth [Royaume-Uni] ; Kamini Kalidas [Royaume-Uni] ; Ghulam Mufti [Royaume-Uni] ; Jackie Cornish [Royaume-Uni] ; Russell Keenan [Royaume-Uni] ; Peter Mortimer (dermatologue) [Royaume-Uni] ; Victoria Murday [Royaume-Uni] | Emberger syndrome—Primary lymphedema with myelodysplasia: Report of seven new cases |
| 006856 (2008) |
Kemal Ni Li [Turquie] ; Naci Oner ; Hülya Kayserili ; Türkan Ertu Rul | [A case of Hennekam syndrome presenting with massive pericardial effusion]. |
| 007258 (2007) |
Mylène Béri-Deixheimer [France] ; Marie-José Gregoire ; Annick Toutain ; Karène Brochet ; Sylvain Briault ; Jean-Luc Schaff ; Bruno Leheup ; Philippe Jonveaux | Genotype-phenotype correlations to aid in the prognosis of individuals with uncommon 20q13.33 subtelomere deletions: a collaborative study on behalf of the 'association des Cytogénéticiens de langue Française'. |
| 007C66 (2006) |
David A. Stevenson [États-Unis] ; Theodore J. Pysher [États-Unis] ; Robert M. Ward [États-Unis] ; John C. Carey [États-Unis] | Familial congenital non‐immune hydrops, chylothorax, and pulmonary lymphangiectasia |
| 008801 (2004) |
Vera Lúcia Gil Da Silva Lopes ; Maria Leine Guion-Almeida ; Silvyo David Araújo Giffoni | Frontonasal dysplasia, neuronal migration error and lymphoedema of limbs. |
| 009581 (2002) |
F. Forzano [Italie] ; F. Faravelli [Italie] ; A. Loy [Italie] ; M. Di Rocco [Italie] | Severe lymphedema, intestinal lymphangiectasia, seizures and mild mental retardation: Further case of Hennekam syndrome with a severe phenotype |
| 00BF55 (1996) |
K. Mishima [Japon] ; T. Sugahara [Japon] ; Y. Mori [Japon] ; M. Sakuda [Japon] | Three cases of oblique facial cleft |
| 00C091 (1996) |
Emily Chen ; Susan K. Larabell ; Jamilyn M. Daniels [États-Unis] ; Stanley Goldstein [États-Unis] | Distichiasis‐lymphedema syndrome: Tetralogy of Fallot, chylothorax, and neonatal death |
| 00D077 (1992) |
J. Stein [États-Unis] ; S J Myers | Spinal cord arteriovenous malformation in a person with congenital lymphatic abnormalities. |
| 00D888 (1991) |
A. B. Jamjoom [Arabie saoudite] ; B. G. Mathew ; H. B. Coakham | A variant of the syndrome of spinal arachnoid cysts with multiple congential defects |
| 00DB76 (1990) |
G. I. Muguti [Zimbabwe] | The amniotic band syndrome: single-stage correction |
| 00EB95 (1986) |
W. Dennis Opitz | Editorial comment on the paper by Crowe and Dickerman: On congenital lymphedema |
| 00EC82 (1985) |
F. Piattoni ; D. Bergonzi ; V. Sala ; F. Argir ; M. Masarone | [Pseudochondroplastic spondyloepiphyseal dysplasia associated with nonfamilial congenital lymphedema and ichthyosis. Description of a case]. |
| 00F621 (1982) |
A A Adeyokunnu | The incidence of Turner's syndrome in Ibadan, Nigeria. |
| 00FA01 (1980) |
M. Burroni ; Q. Catena ; G. Franchi ; U. Gobbi ; F. Perrotta ; T. Ricci ; B. Valentini ; M. Milani Comparetti | [Turner's syndrome in the newborn infant. Description of 3 cases]. |
| 010615 (1974) |
S. Lal ; S. Choudry ; B R Garg ; K K Srivastava | Congenital constrictions. |
| 010A81 (1971) |
R E Hoover ; J S Kelley | Distichiasis and lymphedema: a hereditary syndrome with possible multiple defects. A report of a family. |
| 011610 (1964) |
Harold F. Falls [États-Unis] ; Elsa D. Kertesz [États-Unis] | A New Syndrome Combining Pterygium Colli with Developmental Anomalies of the Eyelids and Lymphatics of the Lower Extremities* |
| 012B38 (????) |
Maria N. Kelly [États-Unis] ; Nausheen Khuddus ; Silus Motamarry ; Sanjeev Tuli | Microcephaly, lymphedema, chorioretinal dysplasia (MLCRD) syndrome. |
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