215 related articles for article (PubMed ID: 14151466)
1. [MOSAIC TRISOMY 21/NORMAL IN A FEMALE INFANT WITH VARIOUS MALFORMATIONS AND SIGNS OF MONGOLISM].
BISCATTI G
Pediatria (Napoli); 1964 Apr; 72():315-8. PubMed ID: 14151466
[No Abstract] [Full Text] [Related]
2. [THE MALFORMATIVE SYNDROME OF CHROMOSOME 18 TRISOMY].
NIGRO N; FRANCESCHINI P; VOLANTE G
Minerva Pediatr; 1964 Apr; 16():471-80. PubMed ID: 14158345
[No Abstract] [Full Text] [Related]
3. A MOSAIC MONGOL WITH NORMAL LEUCOCYTE CHROMOSOMES.
RIDLER MA; SHAPIRO A; DELHANTY JD; SMITH GF
Br J Psychiatry; 1965 Feb; 111():183-5. PubMed ID: 14270531
[No Abstract] [Full Text] [Related]
4. 21 TRISOMY/NORMAL MOSAICISM IN AN INTELLIGENT CHILD WITH SOME MONGOLOID CHARACTERS.
CLARKE CM; FORD CE; EDWARDS JH; SMALLPEICE V
Lancet; 1963 Dec; 2(7319):1229. PubMed ID: 14072963
[No Abstract] [Full Text] [Related]
5. 21-trisomy/normal mosaicism in an intelligent child with some mongoloid characters.
CLARKE CM; EDWARDS JH; SMALLPEICE V
Lancet; 1961 May; 1(7185):1028-30. PubMed ID: 13693884
[No Abstract] [Full Text] [Related]
6. [SYMPOSIUM ON THE GENERAL CARE OF THE NORMAL AND PATHOLOGICAL NEWBORN. II. PATHOLOGY OF THE NEWBORN. B. CONGENITAL MALFORMATIONS: DIAGNOSIS AND MANAGEMENT IN THE NEONATAL PERIOD].
DE PENNA HA; CURTI P; MANISSADJIAN A; BARBIERI D
Rev Paul Med; 1964 Jun; 64():321-407. PubMed ID: 14171499
[No Abstract] [Full Text] [Related]
7. [ATYPICAL FORM OF THE PIERRE ROBIN SYNDROME. PRESENTATION OF 2 CASES].
PERALTASERRANO A
Rev Clin Esp; 1964 Apr; 93():47-50. PubMed ID: 14150288
[No Abstract] [Full Text] [Related]
8. CONGENITAL MALFORMATIONS. CLINICAL AND COMMUNITY CONSIDERATIONS.
INGALLS TH; KLINGBERG MA
Am J Med Sci; 1965 Mar; 249():316-44. PubMed ID: 14273322
[No Abstract] [Full Text] [Related]
9. NORMAL-TRISOMY 13-15 MOSAICISM IN TWO INFANTS.
BAIN AD; INSLEY J; DOUGLAS DM; GAULD IK; SCOTT HA
Arch Dis Child; 1965 Aug; 40(212):442-5. PubMed ID: 14329263
[No Abstract] [Full Text] [Related]
10. Concurrent psu dic(21)(q22.3) and t(13;17)(q14.1;p12) in a mosaic Down's syndrome patient: review of thirty-one similar dicentrics.
Rivera H; Vásquez-Velásquez AI
J Genet; 2014 Apr; 93(1):189-92. PubMed ID: 24840838
[No Abstract] [Full Text] [Related]
11. [ON CONGENITAL FACIAL PARALYSIS].
BALDUS S
Monatsschr Ohrenheilkd Laryngorhinol; 1964 Jan; 98():25-30. PubMed ID: 14182791
[No Abstract] [Full Text] [Related]
12. [Apropos of several congenital malformations observed in the Congo].
BROWNE SG
Ann Soc Belg Med Trop (1920); 1962 Jun; 42():295-8. PubMed ID: 14016081
[No Abstract] [Full Text] [Related]
13. Trisomy 7 mosaicism prenatally misdiagnosed and maternal uniparental disomy in a child with pigmentary mosaicism and Russell- Silver syndrome.
Petit F; Holder-Espinasse M; Duban-Bedu B; Bouquillon S; Boute-Benejean O; Bazin A; Rouland V; Manouvrier-Hanu S; Delobel B
Clin Genet; 2012 Mar; 81(3):265-71. PubMed ID: 21204802
[TBL] [Abstract][Full Text] [Related]
14. Unilateral microtia in an infant with trisomy 18 mosaicism.
Giannatou E; Leze H; Katana A; Kolialexi A; Mavrou A; Kanavakis E; Kitsiou-Tzeli S
Genet Couns; 2009; 20(2):181-7. PubMed ID: 19650416
[TBL] [Abstract][Full Text] [Related]
15. Mosaic trisomy 9 presenting with congenital heart disease, facial dysmorphism and pigmentary skin lesions: intricate issues of genetic counseling.
Patil SJ; Ponnala R; Shah S; Dalal A
Indian J Pediatr; 2012 Jun; 79(6):806-9. PubMed ID: 21975655
[TBL] [Abstract][Full Text] [Related]
16. [RARE MALFORMATIONS OF THE FACE].
MOYSON F; JEANTY M
Arch Fr Pediatr; 1964 Oct; 21():939-55. PubMed ID: 14195289
[No Abstract] [Full Text] [Related]
17. Transient myeloproliferative disorder as the presenting feature for mosaic trisomy 21.
Baca N; Sanchez-Lara PA; Schreck R; Eno CC; Majlessipour F
Cold Spring Harb Mol Case Stud; 2021 Dec; 7(6):. PubMed ID: 34789514
[TBL] [Abstract][Full Text] [Related]
18. Maternal uniparental isodisomy 20 in a foetus with trisomy 20 mosaicism: clinical, cytogenetic and molecular analysis.
Velissariou V; Antoniadi T; Gyftodimou J; Bakou K; Grigoriadou M; Christopoulou S; Hatzipouliou A; Donoghue J; Karatzis P; Katsarou E; Petersen MB
Eur J Hum Genet; 2002 Nov; 10(11):694-8. PubMed ID: 12404100
[TBL] [Abstract][Full Text] [Related]
19. [THE POTTER SYNDROME (BILATERAL RENAL AGENESIS, FACIAL CHANGES AND OLIGOHYDRAMNIOS). STUDY OF A CASE].
RASORE-QUARTINO A; DEPAULINI GC
Pathologica; 1963; 55():459-62. PubMed ID: 14153633
[No Abstract] [Full Text] [Related]
20. MALFORMATIONS OF THE EAR.
WOLFF D
Arch Otolaryngol; 1964 Mar; 79():288-301. PubMed ID: 14090429
[No Abstract] [Full Text] [Related]
[Next] [New Search]