344 related articles for article (PubMed ID: 8031533)
21. The Wolf-Hirschhorn syndrome. Deletion of the short arm of chromosome 4.
Fryns JP; François B; Timmermans J; Emmery L; Speybrouck J; Van Den Berghe H
Acta Paediatr Belg; 1979; 32(2):135-9. PubMed ID: 495091
[No Abstract] [Full Text] [Related]
22. Interstitial deletion of the short arm of chromosome 3 (3p14).
Short MP; Shah KD; Djamdjian S; Dische MR; Gilbert F
Am J Med Genet; 1986 Aug; 24(4):649-52. PubMed ID: 3740098
[TBL] [Abstract][Full Text] [Related]
23. Deletions of different segments of the long arm of chromosome 4.
Mitchell JA; Packman S; Loughman WD; Fineman RM; Zackai E; Patil SR; Emanual B; Bartley JA; Hanson JW
Am J Med Genet; 1981; 8(1):73-89. PubMed ID: 7246608
[TBL] [Abstract][Full Text] [Related]
24. [De novo monosomy 4q32.1 leads to 4qter in a newborn with multiple malformations (author's transl)].
Rethoré MO; Couturier J; Mselati JC; Cochois B; Lavaud J; Lejeune J
Ann Genet; 1979; 22(4):214-6. PubMed ID: 317783
[TBL] [Abstract][Full Text] [Related]
25. De novo deletion of chromosome 9 (9p-) in a child with multiple congenital anomalies and psychomotor retardation.
Murthy DS; Murthy SK; Banker GJ; Patel AJ
Indian Pediatr; 1991 May; 28(5):546-9. PubMed ID: 1684352
[No Abstract] [Full Text] [Related]
26. Angelman's syndrome and 15q11-q13 deletion.
Fryns JP; Kleczowska A; Decock P; van den Berghe H
Genet Couns; 1990; 1(1):57-62. PubMed ID: 2222923
[TBL] [Abstract][Full Text] [Related]
27. Is the autosomal dominant Optiz GBBB syndrome part of the DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2?
Wulfsberg EA
Am J Med Genet; 1996 Aug; 64(3):523-4. PubMed ID: 8862634
[No Abstract] [Full Text] [Related]
28. Small terminal deletions of the long arm of chromosome 2: two new cases.
Fisher AM; Ellis KH; Browne CE; Barber JC; Barker M; Kennedy CR; Foley H; Patton MA
Am J Med Genet; 1994 Dec; 53(4):366-9. PubMed ID: 7532357
[TBL] [Abstract][Full Text] [Related]
29. Interstitial deletion of the long arm of chromosome 11.
Carnevale A; Blanco B; Grether P; Castillejos AR
Ann Genet; 1987; 30(1):56-8. PubMed ID: 3498432
[TBL] [Abstract][Full Text] [Related]
30. [Brachmann-Cornelia de Lange syndrome].
Bonioli E; Bellini C; Ruffa G; Camera G; Gemme G
Minerva Pediatr; 1987 Feb; 39(3-4):135-8. PubMed ID: 3587191
[No Abstract] [Full Text] [Related]
31. 46,XX,der(2)t(2;10)(2pter-->2q37::10p13-->10pter)[127]/45,X,der(2)t(2;10) (2pter-->2q37::10p13-->10pter)[23]. Karyotype-phenotype correlation and genetic counselling in complex karyotypes.
Grammatico P; Majore S; Marrocco G; Poscente M; Mordenti C; Grammatico B; Del Porto G
Genet Couns; 1999; 10(4):351-8. PubMed ID: 10631922
[TBL] [Abstract][Full Text] [Related]
32. Interstitial deletion of chromosome 3p: report of a patient and delineation of a proximal 3p deletion syndrome.
Neri G; Reynolds JF; Westphal J; Hinz J; Daniel A
Am J Med Genet; 1984 Sep; 19(1):189-93. PubMed ID: 6496569
[TBL] [Abstract][Full Text] [Related]
33. A practical application of fluorescent in situ hybridization to the Wolf-Hirschhorn syndrome.
Fagan K; Colley P; Partington M
Pediatrics; 1994 May; 93(5):826-7. PubMed ID: 8165089
[No Abstract] [Full Text] [Related]
34. Loss of the N-myc oncogene in a patient with a small interstitial deletion of the short arm of chromosome 2.
Saal HM; King LJ; Zimmerman D; Johnson RC; Carr AG; Samango-Sprouse CA; Stanley W
Am J Med Genet; 1996 Dec; 66(4):373-7. PubMed ID: 8989454
[TBL] [Abstract][Full Text] [Related]
35. Velocardiofacial syndrome (Shprintzen syndrome, chromosome 22q11 deletion syndrome).
Olney AH; Kolodziej P
Ear Nose Throat J; 1998 Jun; 77(6):460-1. PubMed ID: 9674319
[No Abstract] [Full Text] [Related]
36. Narrowing the deleted region associated with the 15q21 syndrome.
Pramparo T; Mattina T; Gimelli S; Liehr T; Zuffardi O
Eur J Med Genet; 2005; 48(3):346-52. PubMed ID: 16179230
[TBL] [Abstract][Full Text] [Related]
37. [2 new cases of deletion of the short arm of chromosome 9].
Antonenko VG; Demintseva VS; Demina NA; Levina LIa
Pediatriia; 1987; (3):81-4. PubMed ID: 3601545
[No Abstract] [Full Text] [Related]
38. Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion.
McDonald-McGinn DM; Emanuel BS; Zackai EH
Am J Med Genet; 1996 Aug; 64(3):525-6. PubMed ID: 8862635
[No Abstract] [Full Text] [Related]
39. A common region of 10p deleted in DiGeorge and velocardiofacial syndromes.
Daw SC; Taylor C; Kraman M; Call K; Mao J; Schuffenhauer S; Meitinger T; Lipson T; Goodship J; Scambler P
Nat Genet; 1996 Aug; 13(4):458-60. PubMed ID: 8696341
[TBL] [Abstract][Full Text] [Related]
40. Terminal deletion of the long arm of chromosome 10: a new case with breakpoint in q25.3.
Petersen B; Strassburg HM; Feichtinger W; Kress W; Schmid M
Am J Med Genet; 1998 Apr; 77(1):60-2. PubMed ID: 9557896
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]