182 related articles for article (PubMed ID: 6882130)
1. [Association of hereditary hydrocephalus and holoprosencephaly].
Lambert JC; Ferrari M; Donzeau M; Hericort P; Boutte P; Walbaum R; Ayraud N
Arch Fr Pediatr; 1983 May; 40(5):397-9. PubMed ID: 6882130
[TBL] [Abstract][Full Text] [Related]
2. [Association of VACTERL and hydrocephalus: a new familial entity].
Briard ML; le Merrer M; Plauchu H; Dodinval P; Lambotte C; Moraine C; Serville F
Ann Genet; 1984; 27(4):220-3. PubMed ID: 6335367
[TBL] [Abstract][Full Text] [Related]
3. Holoprosencephaly, ear abnormalities, congenital heart defect, and microphallus in a patient with 11q- mosaicism.
Helmuth RA; Weaver DD; Wills ER
Am J Med Genet; 1989 Feb; 32(2):178-81. PubMed ID: 2494886
[TBL] [Abstract][Full Text] [Related]
4. Microcephaly in familial holoprosencephaly.
Ardinger HH; Bartley JA
J Craniofac Genet Dev Biol; 1988; 8(1):53-61. PubMed ID: 3209679
[TBL] [Abstract][Full Text] [Related]
5. Brief clinical report: HARD (+/- E) syndrome: report of a sixth family with support for autosomal-recessive inheritance.
Aymé S; Mattei JF
Am J Med Genet; 1983 Apr; 14(4):759-66. PubMed ID: 6405616
[TBL] [Abstract][Full Text] [Related]
6. Holoprosencephaly and trisomy 21 in a child born to a nondiabetic mother.
Urioste M; Valcarcel E; Gomez MA; Pinel I; Garcia de León R; Diaz de Bustamante A; Tebar R; Martinez-Frias ML
Am J Med Genet; 1988 Aug; 30(4):925-8. PubMed ID: 2973234
[TBL] [Abstract][Full Text] [Related]
7. X-linked aqueductal stenosis.
Sovik O; van der Hagen B; Loken AC
Clin Genet; 1977 Jun; 11(6):416-20. PubMed ID: 301802
[TBL] [Abstract][Full Text] [Related]
8. X-linked VACTERL with hydrocephalus: the VACTERL-H syndrome.
Genuardi M; Chiurazzi P; Capelli A; Neri G
Birth Defects Orig Artic Ser; 1993; 29(1):235-41. PubMed ID: 8280876
[No Abstract] [Full Text] [Related]
9. Single central maxillary incisor and holoprosencephaly.
Hattori H; Okuno T; Momoi T; Kataoka K; Mikawa H; Shiota K
Am J Med Genet; 1987 Oct; 28(2):483-7. PubMed ID: 3425622
[TBL] [Abstract][Full Text] [Related]
10. [General considerations on holoprosencephaly. Description of 2 cases of alobar holoprosencephaly].
Caramia G; Rossi R; Carotti L; Eugeni CE
Minerva Pediatr; 1987 Jan; 39(1-2):37-41. PubMed ID: 3600557
[No Abstract] [Full Text] [Related]
11. [Familial hydrocephalus, recessive hereditary gonosomic disease (Bickers and Adams syndrome)].
Martin C; Got M; Babin JP; Cazauran JM
Arch Fr Pediatr; 1971 Nov; 28(9):971-4. PubMed ID: 5144696
[No Abstract] [Full Text] [Related]
12. [Clinical and etiopathogenetic aspects of lissencephaly type II syndrome].
Mielke R; Lu JH; Kochs G; Kowalewski S
Monatsschr Kinderheilkd; 1987 Nov; 135(11):780-3. PubMed ID: 3431559
[TBL] [Abstract][Full Text] [Related]
13. Aqueductal atresia as a feature of arhinencephalic syndromes.
Vogel H; Gessaga EC; Horoupian DS; Urich H
Clin Neuropathol; 1990; 9(4):191-5. PubMed ID: 2225595
[TBL] [Abstract][Full Text] [Related]
14. Cyclopia-otocephaly association: a new case of the most severe variant of agnathia-holoprosencephaly complex.
Carles D; Serville F; Mainguené M; Dubecq JP
J Craniofac Genet Dev Biol; 1987; 7(2):107-13. PubMed ID: 3114309
[TBL] [Abstract][Full Text] [Related]
15. VACTERL with hydrocephalus: spontaneous chromosome breakage and rearrangement in a family showing apparent sex-linked recessive inheritance.
Wang H; Hunter AG; Clifford B; McLaughlin M; Thompson D
Am J Med Genet; 1993 Aug; 47(1):114-7. PubMed ID: 8368240
[TBL] [Abstract][Full Text] [Related]
16. VACTERL with hydrocephalus: a further case with probable autosomal recessive inheritance.
Corsello G; Giuffrè L
Am J Med Genet; 1994 Jan; 49(1):137-8. PubMed ID: 8172244
[No Abstract] [Full Text] [Related]
17. A novel L1CAM mutation with L1 spectrum disorders.
Silan F; Ozdemir I; Lissens W
Prenat Diagn; 2005 Jan; 25(1):57-9. PubMed ID: 15662685
[TBL] [Abstract][Full Text] [Related]
18. Median cleft face syndrome in association with hydrocephalus, agenesis of the corpus callosum, holoprosencephaly and choanal atresia.
Bömelburg T; Lenz W; Eusterbrock T
Eur J Pediatr; 1987 May; 146(3):301-2. PubMed ID: 3595651
[TBL] [Abstract][Full Text] [Related]
19. Holoprosencephaly and endocrine dysgenesis in brothers.
Begleiter ML; Harris DJ
Am J Med Genet; 1980; 7(3):315-8. PubMed ID: 7193414
[TBL] [Abstract][Full Text] [Related]
20. [The hydrolethalus syndrome--a new hereditary malformation syndrome in Finland].
Salonen R; Herva R; Norio R
Duodecim; 1981; 97(16):1312-9. PubMed ID: 7327122
[No Abstract] [Full Text] [Related]
[Next] [New Search]