Frydman M - Search Results

1

Familial simple hypohidrosis with abnormal palmar dermal ridges.

Frydman M, Cohen HA, Kauschansky A, Matoth Y. Frydman M, et al. Am J Med Genet. 1988 Nov;31(3):591-6. doi: 10.1002/ajmg.1320310313. Am J Med Genet. 1988. PMID: 3228139

2

Váradi syndrome (OFD VI) or Opitz trigonocephaly syndrome: overlapping manifestations in two cousins.

Cleper R, Kauschansky A, Varsano I, Frydman M. Cleper R, et al. Among authors: frydman m. Am J Med Genet. 1993 Sep 15;47(4):451-5. doi: 10.1002/ajmg.1320470402. Am J Med Genet. 1993. PMID: 8256802

3

Leukonychia totalis in two sibs.

Frydman M, Cohen HA. Frydman M, et al. Am J Med Genet. 1993 Sep 15;47(4):540-1. doi: 10.1002/ajmg.1320470420. Am J Med Genet. 1993. PMID: 8256820

4

Familial segregation of cervical ribs, Sprengel anomaly, preaxial polydactyly, anal atresia, and urethral obstruction: a new syndrome?

Frydman M, Cohen HA, Ashkenazi A, Varsano I. Frydman M, et al. Am J Med Genet. 1993 Mar 15;45(6):717-20. doi: 10.1002/ajmg.1320450611. Am J Med Genet. 1993. PMID: 8456850

5

Autosomal recessive Peters anomaly, typical facial appearance, failure to thrive, hydrocephalus, and other anomalies: further delineation of the Krause-Kivlin syndrome.

Frydman M, Weinstock AL, Cohen HA, Savir H, Varsano I. Frydman M, et al. Am J Med Genet. 1991 Jul 1;40(1):34-40. doi: 10.1002/ajmg.1320400107. Am J Med Genet. 1991. PMID: 1887847 Review.

6

Ambiguous genitalia in the Proteus syndrome.

Frydman M, Kauschansky A, Vrsano I. Frydman M, et al. Am J Med Genet. 1990 Aug;36(4):511-2. doi: 10.1002/ajmg.1320360428. Am J Med Genet. 1990. PMID: 2389808

7

Trigonocephaly: a new familial syndrome.

Frydman M, Kauschansky A, Elian E. Frydman M, et al. Am J Med Genet. 1984 May;18(1):55-9. doi: 10.1002/ajmg.1320180109. Am J Med Genet. 1984. PMID: 6741996

8

Familial isolated growth-hormone deficiency with advanced sexual maturation.

Kauschansky A, Cohen HA, Varsano I, Laron Z, Frydman M. Kauschansky A, et al. Among authors: frydman m. Am J Dis Child. 1993 Feb;147(2):170-3. doi: 10.1001/archpedi.1993.02160260060023. Am J Dis Child. 1993. PMID: 8427240

9

MODED: microcephaly-oculo-digito-esophageal-duodenal syndrome.

Frydman M, Katz M, Cabot SG, Soen G, Kauschansky A, Sirota L. Frydman M, et al. Am J Med Genet. 1997 Aug 22;71(3):251-7. doi: 10.1002/(sici)1096-8628(19970822)71:3<251::aid-ajmg1>3.0.co;2-x. Am J Med Genet. 1997. PMID: 9268091

10

Syndrome of alopecia totalis and 17b-hydroxysteroid dehydrogenase deficiency.

Kauschansky A, Shohat M, Frydman M, Rösler A, Greenbaum E, Sirota L. Kauschansky A, et al. Among authors: frydman m. Am J Med Genet. 1998 Feb 26;76(1):28-31. Am J Med Genet. 1998. PMID: 9508060

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