205 related articles for article (PubMed ID: 8897040)
1. A case of achondrogenesis type IA with an occipital encephalocele.
Chen CP; Liu FF; Jan SW; Lin YN; Lan CC
Genet Couns; 1996; 7(3):193-9. PubMed ID: 8897040
[TBL] [Abstract][Full Text] [Related]
2. The boneless neonate: a severe form of achondrogenesis type I.
Jaeger HJ; Schmitz-Stolbrink A; Hulde J; Novak M; Roggenkamp K; Mathias K
Pediatr Radiol; 1994; 24(5):319-21. PubMed ID: 7824361
[TBL] [Abstract][Full Text] [Related]
3. [New subtype of familial achondrogenesis type IA (Houston-Harris)].
Ramírez-García SA; García-Cruz D; Cervantes-Aragón I; Bitar-Alatorre WE; Dávalos-Rodríguez IP; Dávalos-Rodríguez NO; Corona-Rivera JR; Sánchez-Corona J
Cir Cir; 2018; 86(1):89-98. PubMed ID: 29681641
[TBL] [Abstract][Full Text] [Related]
4. Achondrogenesis type II with normally developed extremities: a case report.
Kocakoc E; Kiris A
Prenat Diagn; 2002 Jul; 22(7):594-7. PubMed ID: 12124695
[TBL] [Abstract][Full Text] [Related]
5. [Meckel-Gruber syndrome].
Flessa A; Rempen A; Schmausser B; Marx A
Z Geburtshilfe Neonatol; 1996; 200(2):66-8. PubMed ID: 8767290
[TBL] [Abstract][Full Text] [Related]
6. Rapid detection of K650E mutation in FGFR3 using uncultured amniocytes in a pregnancy affected with fetal cloverleaf skull, occipital pseudoencephalocele, ventriculomegaly, straight short femurs, and thanatophoric dysplasia type II.
Chen CP; Chang TY; Lin MH; Chern SR; Su JW; Wang W
Taiwan J Obstet Gynecol; 2013 Sep; 52(3):420-5. PubMed ID: 24075385
[TBL] [Abstract][Full Text] [Related]
7. Achondrogenesis type II (Langer-Saldino achondrogenesis): a case report.
Lee HS; Doh JW; Kim CJ; Chi JG
J Korean Med Sci; 2000 Oct; 15(5):604-8. PubMed ID: 11069003
[TBL] [Abstract][Full Text] [Related]
8. Achondrogenesis type I. A familial subvariant?
Lauder I; Ellis HA; Ashcroft T; Burridge A
Arch Dis Child; 1976 Jul; 51(7):550-7. PubMed ID: 962365
[TBL] [Abstract][Full Text] [Related]
9. Goldston syndrome reconsidered.
Moerman P; Pauwels P; Vandenberghe K; Lauweryns JM; Fryns JP
Genet Couns; 1993; 4(2):97-102. PubMed ID: 8357569
[TBL] [Abstract][Full Text] [Related]
10. Lethal short-limbed chondrodysplasia in early infancy.
Yang SS; Heidelberger KP; Brough AJ; Corbett DP; Bernstein J
Perspect Pediatr Pathol; 1976; 3():1-40. PubMed ID: 972830
[TBL] [Abstract][Full Text] [Related]
11. Cephalocele detection in utero: sonographic and clinical features.
Budorick NE; Pretorius DH; McGahan JP; Grafe MR; James HE; Slivka J
Ultrasound Obstet Gynecol; 1995 Feb; 5(2):77-85. PubMed ID: 7719871
[TBL] [Abstract][Full Text] [Related]
12. [Iniencephaly: description of a case].
Zatterale A; Della Pietra B; Perna A; Pozzolo S; Camera G
Pathologica; 1995 Dec; 87(6):726-8. PubMed ID: 8927443
[TBL] [Abstract][Full Text] [Related]
13. Pseudo-achondrogenesis with fractures.
Harris R; Patton JT; Barson AJ
Clin Genet; 1972; 3(6):435-41. PubMed ID: 4568361
[No Abstract] [Full Text] [Related]
14. Neonatal death dwarfism. (A further report).
Kozlowski K; Masel J; Morris L; Kunze D
Rofo; 1978 Nov; 129(5):626-33. PubMed ID: 152275
[TBL] [Abstract][Full Text] [Related]
15. Achondroplasia-hypochondroplasia complex in a newborn infant.
Huggins MJ; Smith JR; Chun K; Ray PN; Shah JK; Whelan DT
Am J Med Genet; 1999 Jun; 84(5):396-400. PubMed ID: 10360392
[TBL] [Abstract][Full Text] [Related]
16. Achondrogenesis Type IA (Houston-Harris): a still-unresolved molecular phenotype.
Aigner T; Rau T; Niederhagen M; Zaucke F; Schmitz M; Pöhls U; Stöss H; Rauch A; Thiel CT
Pediatr Dev Pathol; 2007; 10(4):328-34. PubMed ID: 17638425
[TBL] [Abstract][Full Text] [Related]
17. Achondrogenesis type II with cutaneous hamartomata.
Wainwright H; Beighton P
Clin Dysmorphol; 2008 Jul; 17(3):207-209. PubMed ID: 18541971
[No Abstract] [Full Text] [Related]
18. Bone dysplasia series. Achondroplasia, hypochondroplasia and thanatophoric dysplasia: review and update.
Lemyre E; Azouz EM; Teebi AS; Glanc P; Chen MF
Can Assoc Radiol J; 1999 Jun; 50(3):185-97. PubMed ID: 10405653
[TBL] [Abstract][Full Text] [Related]
19. [Combination of Cantrell pentalogy and amniotic band syndrome: a case report].
Schüppler U; Weisner D; Schollmeyer T; Grillo M; Franz W
Zentralbl Gynakol; 1994; 116(2):115-9. PubMed ID: 8147187
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of recurrent Meckel syndrome.
Ramadani HM; Nasrat HA
Int J Gynaecol Obstet; 1992 Dec; 39(4):327-32. PubMed ID: 1361467
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]