49 related articles for article (PubMed ID: 7473664)
1. Myeloblastic leukemia and congenital hemihypertrophy.
Vergara B; Svarch E
J Pediatr; 1977 Jun; 90(6):1036-7. PubMed ID: 192872
[No Abstract] [Full Text] [Related]
2. Filippi syndrome: Three new families suggest that urinary system abnormalities may belong to clinical spectrum of the disease.
Bas H; Durmaz CD; Tombak MC; Cetin GO; Karaer K
Am J Med Genet A; 2024 May; ():e63654. PubMed ID: 38738944
[TBL] [Abstract][Full Text] [Related]
3. Filippi Syndrome: Report of a Rare Case.
Goyal L; Goyal JP; Bhakhri BK; Chug A
J Clin Diagn Res; 2015 Dec; 9(12):SD01-3. PubMed ID: 26813917
[TBL] [Abstract][Full Text] [Related]
4. Multiple dental and skeletal abnormalities in an individual with filippi syndrome.
Sandhu M; Malik P; Saha R
Case Rep Dent; 2013; 2013():845405. PubMed ID: 24222867
[TBL] [Abstract][Full Text] [Related]
5. Filippi syndrome: a new case with skeletal abnormalities.
Héron D; Billette de Villemeur T; Munnich A; Lyonnet S
J Med Genet; 1995 Aug; 32(8):659-61. PubMed ID: 7473664
[TBL] [Abstract][Full Text] [Related]
6. Filippi syndrome: further clinical characterization.
Battaglia A; Filippi T; Pusceddu S; Williams CA
Am J Med Genet A; 2008 Jul; 146A(14):1848-52. PubMed ID: 18553552
[TBL] [Abstract][Full Text] [Related]
7. Filippi syndrome: report of three additional cases.
Williams MS; Williams JL; Wargowski DS; Pauli RM; Pletcher BA
Am J Med Genet; 1999 Nov; 87(2):128-33. PubMed ID: 10533026
[TBL] [Abstract][Full Text] [Related]
8. Identification of a novel pathogenic variant in CKAP2L and literature review in a child with Filippi syndrome and congenital talipes equinovarus.
Karakaya T; Bilgic AE; Eris D; Baser B; Mermer S; Yildiz O
Am J Med Genet A; 2021 Jul; 185(7):2198-2203. PubMed ID: 33913579
[TBL] [Abstract][Full Text] [Related]
9. Microcephaly, mild mental retardation, short stature, and skeletal anomalies in siblings.
Zackai EH; Sly WS; McAlister WG
Am J Dis Child; 1972 Jul; 124(1):111-5. PubMed ID: 5033742
[No Abstract] [Full Text] [Related]
10. Short stature, microcephaly, characteristic face, syndactyly and mental retardation: the Filippi syndrome. Report on a second family.
Meinecke P
Genet Couns; 1993; 4(2):147-51. PubMed ID: 8395190
[TBL] [Abstract][Full Text] [Related]
11. Craniodigital syndromes: report of a child with Filippi syndrome and discussion of differential diagnosis.
Toriello HV; Higgins JV
Am J Med Genet; 1995 Jan; 55(2):200-4. PubMed ID: 7717418
[TBL] [Abstract][Full Text] [Related]
12. Unusual facial appearance, microcephaly, growth and mental retardation, and syndactyly. A new syndrome?
Filippi G
Am J Med Genet; 1985 Dec; 22(4):821-4. PubMed ID: 4073130
[TBL] [Abstract][Full Text] [Related]
13.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
14.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
15.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
