Benítez J - Search Results

1

[Prenatal diagnosis of hemophilia A by DNA analysis. First experience in Spain].

Baiget M, Nunes V, del Río E, Ramos C, Ayuso C, Benítez J, Díaz Recasens J. Baiget M, et al. Among authors: benitez j. Med Clin (Barc). 1987 May 16;88(19):770-2. Med Clin (Barc). 1987. PMID: 3613722 Spanish. No abstract available.

2

[Prenatal diagnosis in a family carrying the fragile X syndrome using recombinant DNA technics].

Benítez J, Fernández E, Ramos C, Nunes V, del Río E, Baiget M. Benítez J, et al. Rev Clin Esp. 1989 Apr;184(7):364-6. Rev Clin Esp. 1989. PMID: 2570446 Spanish.

3

[A clinical, cytogenetic and molecular study of 10 patients with the Prader-Willi syndrome].

Barabash A, Robledo M, Sanz R, Renedo M, Ramos C, Ayuso C, Benítez J. Barabash A, et al. Among authors: benitez j. Med Clin (Barc). 1997 Mar 1;108(8):304-6. Med Clin (Barc). 1997. PMID: 9121208 Spanish.

4

[DNA markers linked to Huntington's disease (D4S10 and D4S95) in Spanish families: preliminary results].

Benítez J, Ramos C, Fernández E, Ayuso C, Yébenes J. Benítez J, et al. Rev Clin Esp. 1992 Apr;190(6):299-301. Rev Clin Esp. 1992. PMID: 1350862 Spanish.

5

[Early cytogenetic diagnosis by chorion biopsy. Preliminary communication].

Ramos C, Recasens JD, Benítez J, Santaolaya J, Sánchez Cascos A. Ramos C, et al. Among authors: benitez j. Rev Clin Esp. 1984 Jul 15-31;174(1-2):21-3. Rev Clin Esp. 1984. PMID: 6515061 Spanish. No abstract available.

6

Study of the parental origin of sexual aneuploidy in ten families using RFLPs.

Villamar M, Fernandez E, Ayuso C, Ramos C, Benitez J. Villamar M, et al. Among authors: benitez j. Ann Genet. 1990;33(1):29-31. Ann Genet. 1990. PMID: 1973343

7

[The Pro347Leu mutation of the rhodopsin gene in a Spanish family with autosomal dominant pigmentary retinosis].

Trujillo MJ, del Río T, Reig C, Benítez J, García Sandoval B, Carballo M, Ayuso C. Trujillo MJ, et al. Among authors: benitez j. Med Clin (Barc). 1998 Apr 18;110(13):501-4. Med Clin (Barc). 1998. PMID: 9611733 Spanish.

8

Delta F508 gene deletion and prenatal diagnosis of cystic fibrosis in Italian and Spanish families.

Novelli G, Sangiuolo F, Dallapiccola B, Gasparini P, Savoia A, Pignatti PF, Fernandez E, Benitez J, Casals T, Nunes V, et al. Novelli G, et al. Among authors: benitez j. Prenat Diagn. 1990 Jun;10(6):413-4. doi: 10.1002/pd.1970100609. Prenat Diagn. 1990. PMID: 2217081 No abstract available.

9

Somatic stability in chorionic villi samples and other Huntington fetal tissues.

Benitez J, Robledo M, Ramos C, Ayuso C, Astarloa R, Garcia Yébenes J, Brambati B. Benitez J, et al. Hum Genet. 1995 Aug;96(2):229-32. doi: 10.1007/BF00207386. Hum Genet. 1995. PMID: 7635477

10

Parental origin of chromosomal nondisjunction in a 49,XXXXY male using recombinant-DNA techniques.

Villamar M, Benitez J, Fernández E, Ayuso C, Ramos C. Villamar M, et al. Among authors: benitez j. Clin Genet. 1989 Sep;36(3):152-5. doi: 10.1111/j.1399-0004.1989.tb03181.x. Clin Genet. 1989. PMID: 2791329

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